Chemokine CCL27
Chemokine CCL21
Chemokine CCL22
Chemokine CCL17
Chemokine CCL2
Chemokine CCL19
Chemokine CCL5
Chemokine CCL20
Chemokine CCL1
Chemokines, CC
Receptors, Chemokine
Chemokine CCL3
Chemokine CCL7
Chemokines
Receptors, CCR10
Chemokine CCL4
Chemokine CXCL12
Receptors, CCR1
Chemokine CXCL10
Chemokine CCL8
Receptors, CCR2
Chemokine CCL11
Chemokine CCL24
Receptors, CCR7
Receptors, CCR8
Chemokine CXCL1
Chemotaxis, Leukocyte
Receptors, CCR4
Chemokines, CXC
Chemokine CX3CL1
Macrophage Inflammatory Proteins
Receptors, CCR5
Receptors, CCR3
Mice, Inbred C57BL
Cell Movement
Chemokine CXCL2
Chemokine CXCL13
Receptors, CXCR4
Chemokine CXCL11
Chemotaxis
Chemokine CXCL6
Cells, Cultured
Dendritic Cells
Chemokine CXCL5
Cytokines
Mice, Knockout
Receptors, CXCR3
Mice, Inbred BALB C
Monocytes
Macrophages
Gene Expression Regulation
RNA, Messenger
T-Lymphocytes
Inflammation
Reverse Transcriptase Polymerase Chain Reaction
Enzyme-Linked Immunosorbent Assay
Flow Cytometry
Receptors, Interleukin-8B
Signal Transduction
Dermatitis, Atopic
Up-Regulation
Monocyte Chemoattractant Proteins
Disease Models, Animal
Skin
Mice, Transgenic
Interleukin-8
Ligands
Receptors, CCR6
CD4-Positive T-Lymphocytes
Receptors, Interleukin-8A
Lymph Nodes
NF-kappa B
Carbon Tetrachloride
Immunohistochemistry
Receptors, Cytokine
T-Lymphocytes, Regulatory
Tumor Necrosis Factor-alpha
Chemokines, CX3C
Receptors, CXCR5
Protein Binding
Chemotactic Factors
CD8-Positive T-Lymphocytes
Endothelial Cells
Lymphocyte Activation
Monokines
Receptors, HIV
Carbon Tetrachloride Poisoning
Duffy Blood-Group System
Chemotactic Factors, Eosinophil
Neutrophil Infiltration
Neutrophils
Heterocyclic Compounds
Lung
Leukocytes
Gene Expression
Inflammation Mediators
Interferon-gamma
Th2 Cells
Cell Migration Inhibition
HIV-1
Molecular Sequence Data
Eosinophils
Intercellular Signaling Peptides and Proteins
Lipopolysaccharides
Down-Regulation
Amino Acid Sequence
Epithelial Cells
Leukocytes, Mononuclear
Th1 Cells
Lymphoid Tissue
T-Lymphocyte Subsets
Gene Expression Profiling
Platelet Factor 4
Stromal Cells
Immunity, Innate
Bronchoalveolar Lavage Fluid
Transfection
Drug-Induced Liver Injury
Endothelium, Lymphatic
Expression and cellular localization of the CC chemokines PARC and ELC in human atherosclerotic plaques. (1/275)
Local immune responses are thought to play an important role in the development of atherosclerosis. Histological studies have shown that human atherosclerotic lesions contain T lymphocytes throughout all stages of development, many of which are in an activated state. A number of novel CC chemokines have been described recently, which are potent chemoattractants for lymphocytes: PARC (pulmonary and activation-regulated chemokine), ELC (EBI1-ligand chemokine), LARC (liver and activation-regulated chemokine), and SLC (secondary lymphoid-tissue chemokine). Using reverse transcriptase-polymerase chain reaction and in situ hybridization, we have found gene expression for PARC and ELC but not for LARC or SLC in human atherosclerotic plaques. Immunohistochemical staining of serial plaque sections with specific cell markers revealed highly different expression patterns of PARC and ELC. PARC mRNA was restricted to CD68+ macrophages (n = 14 of 18), whereas ELC mRNA was widely expressed by macrophages and intimal smooth muscle cells (SMC) in nearly all of the lesions examined (n = 12 of 14). ELC mRNA was also found to be expressed in the medial SMC wall of highly calcified plaques (n = 4). Very low levels of ELC mRNA expression could also be detected in normal mammary arteries but no mRNA expression for PARC was detected in these vessels (n = 4). In vitro, ELC mRNA was found to be up-regulated in aortic SMC stimulated with tumor necrosis factor-a and interferon-gamma but not in SMC stimulated with serum. Both PARC and ELC mRNA were expressed by monocyte-derived macrophages but not monocytes. The expression patterns of PARC and ELC mRNA in human atherosclerotic lesions suggest a potential role for these two recently described CC chemokines in attracting T lymphocytes into atherosclerotic lesions. (+info)Cutting edge: immature dendritic cells generated from monocytes in the presence of TGF-beta 1 express functional C-C chemokine receptor 6. (2/275)
Although CD34+ progenitor-derived immature dendritic cells (DCs) express CCR6, several recent studies reported that monocyte-derived immature DCs do not do so. We observed that DCs generated from monocytes in the presence of GM-CSF, IL-4, and TGF-beta 1 consistently responded to liver and activation-regulated chemokine (LARC, also known as macrophage inflammatory protein-3 alpha). These immature DCs expressed one class of high-affinity binding sites for LARC, and expressed both CCR6 mRNA and protein. Therefore, LARC-CCR6 interaction presumably also contributes to the regulation of trafficking of monocyte-derived DCs, and utilization of TGF-beta can potentially provide a ready source of CCR6+ monocyte-derived DCs for therapeutic purposes. (+info)Beta-defensins: linking innate and adaptive immunity through dendritic and T cell CCR6. (3/275)
Defensins contribute to host defense by disrupting the cytoplasmic membrane of microorganisms. This report shows that human beta-defensins are also chemotactic for immature dendritic cells and memory T cells. Human beta-defensin was selectively chemotactic for cells stably transfected to express human CCR6, a chemokine receptor preferentially expressed by immature dendritic cells and memory T cells. The beta-defensin-induced chemotaxis was sensitive to pertussis toxin and inhibited by antibodies to CCR6. The binding of iodinated LARC, the chemokine ligand for CCR6, to CCR6-transfected cells was competitively displaced by beta-defensin. Thus, beta-defensins may promote adaptive immune responses by recruiting dendritic and T cells to the site of microbial invasion through interaction with CCR6. (+info)MIP-3alpha induces human eosinophil migration and activation of the mitogen-activated protein kinases (p42/p44 MAPK). (4/275)
The CC chemokine macrophage inflammatory protein-3alpha (MIP-3alpha) is the product of recent electronic cloning efforts, however, little characterization of its spectrum of biological effects has been undertaken. Human eosinophils exhibited pertussis-toxin-sensitive migration in response to human recombinant (hr)MIP-3alpha. Messenger RNA for the MIP-3alpha receptor, CCR-6, and low levels of surface expression were demonstrated by reverse transcriptase-polymerase chain reaction and FACS analysis. Analyses of cell signaling revealed dose-dependent increases in intracellular calcium mobilization, calcium transients that were, however, greatly reduced when compared with MCP-3-induced responses. Further investigations of MIP-3alpha-induced signal transduction revealed time- and dose-dependent, partially pertussis toxin-dependent, increases in phosphorylation of the p42/p44 mitogen-activated protein kinases (MAPK) that occurred at 10- to 100-fold lower concentrations, and that were linked to a phosphoinositide 3-kinase pathway. These results suggest that MIP-3alpha can regulate multiple, parallel signal transduction pathways in eosinophils, and suggest that MAPK activation by MIP-3alpha in eosinophils is a significant signaling pathway for migration induction. (+info)In breast carcinoma tissue, immature dendritic cells reside within the tumor, whereas mature dendritic cells are located in peritumoral areas. (5/275)
We have analyzed the presence of immature and mature dendritic cells (DCs) within adenocarcinoma of the breast using immunohistochemistry. Immature DCs were defined by expression of CD1a-, Langerin-, and intracellular major histocompatibility complex class II-rich vesicles. Mature DCs were defined by expression of CD83 and DC-Lamp. Breast carcinoma cells were defined by morphology and/or cytokeratin expression. We demonstrate two levels of heterogeneity of DCs infiltrating breast carcinoma tissue: (a) immature CD1a(+) DCs, mostly of the Langerhans cell type (Langerin(+)), were retained within the tumor bed in 32/32 samples and (b) mature DCs, CD83(+)DC-Lamp(+), present in 20/32 samples, are confined to peritumoral areas. The high numbers of immature DCs found in the tumor may be best explained by high levels of macrophage inflammatory protein 3alpha expression by virtually all tumor cells. Confirming the immature/mature DC compartmentalization pattern, in vitro-generated immature DCs adhere to the tumor cells, whereas mature DCs adhere selectively to peritumoral areas. In some cases, T cells are clustering around the mature DCs in peritumoral areas, thus resembling the DC-T cell clusters of secondary lymphoid organs, which are characteristic of ongoing immune reactions. (+info)Down-regulation of the beta-chemokine receptor CCR6 in dendritic cells mediated by TNF-alpha and IL-4. (6/275)
Chemokines are involved in the control of dendritic cell (DC) trafficking, which is critical for the immune response. We have generated DC from human umbilical cord blood CD34+ progenitors cultured with granulocyte-macrophage colony-stimulating factor, tumor necrosis factor alpha (TNF-alpha), and stem cell factor. Using an anti-CCR6 monoclonal antibody, we observed that these cells showed maximum expression of this beta-chemokine receptor when they were immature, as determined by their relatively low expression of several DC maturation markers such as CD1a, CD11c, CD14, CD40, CD80, and CD83. Immature DC responded strongly to macrophage inflammatory protein-3alpha (MIP-3alpha), the CCR6 ligand, in migration and calcium mobilization assays. CCR6 expression decreased in parallel with the DC maturation induced by prolonged TNF-alphaq treatments. Interleukin-4 was also able to decrease CCR6 protein levels. Our findings suggest that the MIP-3alpha/CCR6 interaction plays an important role in the trafficking of immature DC to chemokine production sites such as injured or inflamed peripheral tissues, where DC undergo maturation on contact with antigens. (+info)Macrophage inflammatory protein 3alpha is involved in the constitutive trafficking of epidermal langerhans cells. (7/275)
Certain types of dendritic cells (DCs) appear in inflammatory lesions of various etiologies, whereas other DCs, e.g., Langerhans cells (LCs), populate peripheral organs constitutively. Until now, the molecular mechanism behind such differential behavior has not been elucidated. Here, we show that CD1a(+) LC precursors respond selectively and specifically to the CC chemokine macrophage inflammatory protein (MIP)-3alpha. In contrast, CD14(+) precursors of DC and monocytes are not attracted by MIP-3alpha. LCs lose the migratory responsiveness to MIP-3alpha during their maturation, and non-LC DCs do not acquire MIP-3alpha sensitivity. The notion that MIP-3alpha may be responsible for selective LC recruitment into the epidermis is further supported by the following observations: (a) MIP-3alpha is expressed by keratinocytes and venular endothelial cells in clinically normal appearing human skin; (b) LCs express CC chemokine receptor (CCR)6, the sole MIP-3alpha receptor both in situ and in vitro; and (c) non-LC DCs that are not found in normal epidermis lack CCR6. The mature forms of LCs and non-LC DCs display comparable sensitivity for MIP-3beta, a CCR7 ligand, suggesting that DC subtype-specific chemokine responses are restricted to the committed precursor stage. Although LC precursors express primarily CCR6, non-LC DC precursors display a broad chemokine receptor repertoire. These findings reflect a scenario where the differential expression of chemokine receptors by two different subpopulations of DCs determines their functional behavior. One type, the LC, responds to MIP-3alpha and enters skin to screen the epidermis constitutively, whereas the other type, the "inflammatory" DC, migrates in response to a wide array of different chemokines and is involved in the amplification and modulation of the inflammatory tissue response. (+info)The exodus subfamily of CC chemokines inhibits the proliferation of chronic myelogenous leukemia progenitors. (8/275)
Chemokines are a family of related proteins that regulate leukocyte infiltration into inflamed tissue and play important roles in disease processes. Among the biologic activities of chemokines is inhibition of proliferation of normal hematopoietic progenitors. However, chemokines that inhibit normal progenitors rarely inhibit proliferation of hematopoietic progenitors from patients with chronic myelogenous leukemia (CML). We and others recently cloned a subfamily of CC chemokines that share similar amino-terminal peptide sequences and a remarkable ability to chemoattract T cells. These chemokines, Exodus-1/LARC/MIP-3alpha, Exodus-2/SLC/6Ckine/TCA4, and Exodus-3/CKbeta11/MIP-3beta, were found to inhibit proliferation of normal human marrow progenitors. The study described here found that these chemokines also inhibited the proliferation of progenitors in every sample of marrow from patients with CML that was tested. This demonstration of consistent inhibition of CML progenitor proliferation makes the 3 Exodus chemokines unique among chemokines. (Blood. 2000;95:1506-1508) (+info)Chemokine CCL27, also known as interleukin-17E (IL-17E), is a type of cytokine that plays a role in the immune system. It is a member of the C-C chemokine family, which is a group of proteins that help to regulate the movement of immune cells within the body. CCL27 is primarily produced by cells of the immune system, including T cells and dendritic cells, and it is involved in the recruitment and activation of immune cells in response to infection or inflammation. It is also involved in the development and function of certain types of immune cells, such as Th17 cells, which play a role in the immune response to pathogens. In the medical field, CCL27 has been studied in relation to a number of different conditions, including psoriasis, atopic dermatitis, and inflammatory bowel disease. It is thought to play a role in the development and progression of these conditions by promoting inflammation and immune cell recruitment to the affected tissues.
Chemokine CCL21 is a type of protein that plays a role in the immune system. It is also known as Exodus-2, 6Ckine, and CC chemokine ligand 21. CCL21 is produced by cells in the lymphatic system and is involved in the recruitment and migration of immune cells, such as T cells and B cells, to specific areas of the body where they are needed. It does this by binding to specific receptors on the surface of these cells, which triggers a signaling cascade that leads to their movement. CCL21 is also involved in the development and maintenance of immune system tissues, such as lymph nodes and the spleen. In the medical field, CCL21 is being studied as a potential target for the treatment of various diseases, including cancer, autoimmune disorders, and infectious diseases.
Chemokine CCL22, also known as macrophage inflammatory protein 13 (MIP-13), is a type of chemokine protein that plays a role in the immune system. It is produced by various cells, including macrophages, dendritic cells, and T cells, and is involved in the recruitment and activation of immune cells to sites of inflammation or infection. CCL22 is a small protein that binds to specific receptors on the surface of immune cells, such as CCR4, and acts as a chemoattractant, guiding these cells to the site of inflammation. It has been implicated in a number of immune-related disorders, including asthma, allergies, and certain types of cancer. In the medical field, CCL22 is often studied as a potential target for the development of new therapies for these and other conditions. For example, drugs that block the interaction between CCL22 and its receptors have been shown to reduce inflammation and improve symptoms in animal models of asthma and other immune disorders.
Chemokine CCL17, also known as TARC (Thymus and Activation-Related Chemokine), is a type of chemokine that plays a role in the immune system. It is a small protein that is produced by various cells, including T cells, B cells, and dendritic cells, and is involved in the recruitment and activation of immune cells, particularly T cells, to sites of inflammation or infection. CCL17 is a chemoattractant, meaning that it attracts immune cells to a specific location in the body. It does this by binding to specific receptors on the surface of immune cells, which triggers a signaling cascade that leads to the movement of the cells towards the source of the chemokine. CCL17 has been implicated in a number of different diseases and conditions, including asthma, atopic dermatitis, and certain types of cancer. In asthma, for example, CCL17 is thought to play a role in the recruitment of T cells to the airways, which can contribute to inflammation and airway remodeling. In atopic dermatitis, CCL17 is thought to contribute to the recruitment of immune cells to the skin, which can lead to itching and inflammation. In cancer, CCL17 has been shown to promote the growth and spread of certain types of tumors by recruiting immune cells to the tumor site and promoting angiogenesis, the formation of new blood vessels.
Chemokine CCL2, also known as monocyte chemoattractant protein-1 (MCP-1), is a small protein that plays a crucial role in the immune system. It is a member of the chemokine family of proteins, which are responsible for regulating the movement of immune cells within the body. CCL2 is primarily produced by cells such as monocytes, macrophages, and endothelial cells in response to inflammatory stimuli. It functions as a chemoattractant, drawing immune cells towards the site of inflammation or infection. Specifically, CCL2 attracts monocytes and T cells to the site of injury or infection, where they can help to clear the infection and promote tissue repair. In addition to its role in immune cell recruitment, CCL2 has also been implicated in a variety of other physiological processes, including angiogenesis (the formation of new blood vessels), tissue repair, and cancer progression. Dysregulation of CCL2 expression or function has been linked to a number of diseases, including atherosclerosis, diabetes, and certain types of cancer.
Chemokine CCL19, also known as Exodus-2, is a type of chemokine protein that plays a role in the immune system. It is a small signaling molecule that is produced by various cells in the body, including immune cells such as dendritic cells and T cells. CCL19 is involved in the recruitment and migration of immune cells to specific areas of the body, such as the lymph nodes and the spleen. It does this by binding to specific receptors on the surface of immune cells, which triggers a signaling cascade that leads to the movement of the cells towards the source of the chemokine. In the medical field, CCL19 is of interest because it has been implicated in a number of different diseases and conditions, including cancer, autoimmune disorders, and infectious diseases. For example, CCL19 has been shown to play a role in the spread of cancer cells to other parts of the body, and it may also be involved in the development of certain autoimmune diseases such as multiple sclerosis. As such, CCL19 is a potential target for the development of new therapies for these conditions.
Chemokine CCL5, also known as RANTES (regulated on activation, normal T cell expressed and secreted), is a small protein that plays a role in the immune system. It is a type of chemokine, which are signaling molecules that help to direct the movement of immune cells to specific areas of the body in response to infection or injury. CCL5 is produced by a variety of cells, including immune cells such as T cells, macrophages, and dendritic cells, as well as non-immune cells such as endothelial cells and fibroblasts. It acts on specific receptors on the surface of immune cells to attract them to the site of infection or injury. CCL5 has been implicated in a number of different diseases and conditions, including asthma, chronic obstructive pulmonary disease (COPD), and certain types of cancer. It is also involved in the recruitment of immune cells to sites of inflammation, and has been shown to play a role in the development of autoimmune diseases such as rheumatoid arthritis. Overall, CCL5 is an important molecule in the immune system that helps to regulate the movement of immune cells and plays a role in the body's response to infection and injury.
Chemokine CCL20, also known as macrophage inflammatory protein 3 alpha (MIP-3α), is a small protein that plays a role in the immune system. It is a type of chemokine, which are signaling molecules that help to direct the movement of immune cells to specific areas of the body in response to infection or injury. CCL20 is produced by a variety of cells, including macrophages, dendritic cells, and epithelial cells. It is involved in the recruitment of immune cells, such as T cells and B cells, to the lymph nodes and other areas of the body where they can help to fight infection. In the context of the medical field, CCL20 has been studied in relation to a number of different conditions, including cancer, autoimmune diseases, and infectious diseases. For example, CCL20 has been shown to play a role in the development and progression of certain types of cancer, such as breast cancer and lung cancer. It has also been implicated in the pathogenesis of autoimmune diseases, such as multiple sclerosis, and in the recruitment of immune cells to sites of infection. Overall, CCL20 is an important molecule in the immune system that helps to regulate the movement of immune cells and plays a role in the body's response to infection and injury.
Chemokine CCL1, also known as macrophage inflammatory protein 1 alpha (MIP-1α), is a type of chemokine protein that plays a role in the immune system. It is produced by various cells, including macrophages, monocytes, and T cells, and is involved in the recruitment and activation of immune cells to sites of inflammation or infection. CCL1 is a small protein that binds to specific receptors on the surface of immune cells, triggering a signaling cascade that leads to the movement of the cells towards the source of the chemokine. This process is known as chemotaxis. In the context of the medical field, CCL1 has been studied for its potential role in various diseases, including cancer, autoimmune disorders, and infectious diseases. For example, high levels of CCL1 have been associated with the progression of certain types of cancer, such as breast and lung cancer. Additionally, CCL1 has been shown to play a role in the recruitment and activation of immune cells in autoimmune disorders such as rheumatoid arthritis and multiple sclerosis. Overall, CCL1 is an important molecule in the immune system and its study may provide insights into the development of new treatments for various diseases.
Chemokines, CC are a family of small proteins that play a crucial role in the immune system by regulating the movement of immune cells, such as white blood cells, to specific areas of the body in response to infection or injury. They are classified based on the number of cysteine residues in their amino acid sequence, with CC chemokines having two cysteines at the amino terminus. CC chemokines are involved in the recruitment of immune cells to sites of inflammation and are also involved in the development of certain types of cancer.
Receptors, Chemokine are proteins found on the surface of cells that bind to specific chemokines, which are small signaling molecules that play a role in immune cell trafficking and inflammation. These receptors are involved in the regulation of immune cell migration and are important for the recruitment of immune cells to sites of infection or injury. There are several different types of chemokine receptors, each of which is specific to a particular chemokine or group of chemokines. Dysregulation of chemokine receptors has been implicated in a variety of diseases, including cancer, autoimmune disorders, and infectious diseases.
Chemokine CCL3, also known as macrophage inflammatory protein 1α (MIP-1α), is a type of chemokine protein that plays a role in the immune system. It is produced by various cells, including macrophages, monocytes, and dendritic cells, in response to infection or inflammation. CCL3 functions as a chemoattractant, drawing immune cells to the site of infection or injury. It also has other functions, such as promoting the activation and differentiation of immune cells, and regulating the inflammatory response. In the medical field, CCL3 is often studied in the context of various diseases, including HIV/AIDS, cancer, and autoimmune disorders. For example, high levels of CCL3 have been associated with poor outcomes in HIV/AIDS, and it has been proposed as a potential therapeutic target for the disease. Additionally, CCL3 has been implicated in the development and progression of certain types of cancer, such as breast cancer and lung cancer.
Chemokine CCL7, also known as monocyte chemoattractant protein-1 (MCP-1), is a small protein that plays a role in the immune system. It is a type of chemokine, which are a group of signaling molecules that help to direct the movement of immune cells to specific areas of the body in response to infection or injury. CCL7 is produced by a variety of cells, including monocytes, macrophages, and endothelial cells, and it is involved in the recruitment of monocytes and other immune cells to sites of inflammation. It does this by binding to specific receptors on the surface of immune cells, which triggers a signaling cascade that leads to the activation and movement of these cells. In the medical field, CCL7 is often studied in the context of various diseases and conditions, including cancer, autoimmune disorders, and infectious diseases. For example, high levels of CCL7 have been associated with the development and progression of certain types of cancer, such as breast cancer and lung cancer. It is also involved in the recruitment of immune cells to sites of inflammation in autoimmune disorders, such as rheumatoid arthritis, and it plays a role in the immune response to infections, such as tuberculosis. Overall, CCL7 is an important molecule in the immune system that helps to regulate the movement of immune cells to specific areas of the body. It is involved in a variety of physiological processes and has been implicated in the development and progression of certain diseases and conditions.
Chemokines are a family of small signaling proteins that play a crucial role in the immune system. They are produced by various cells in response to infection, injury, or inflammation and act as chemical messengers to attract immune cells to the site of injury or infection. Chemokines bind to specific receptors on the surface of immune cells, such as neutrophils, monocytes, and lymphocytes, and guide them to the site of infection or injury. They also play a role in regulating the migration and activation of immune cells within tissues. In the medical field, chemokines are important for understanding and treating various diseases, including cancer, autoimmune disorders, and infectious diseases. They are also being studied as potential therapeutic targets for the development of new drugs to treat these conditions.
Receptors, CCR10 are a type of cell surface receptor protein that are expressed on certain immune cells, such as T cells and B cells. They are activated by a specific chemokine called CCL27, which is produced by cells in the skin and other tissues. Activation of CCR10 receptors by CCL27 has been shown to play a role in the recruitment of immune cells to the skin, and is thought to be involved in the development of certain skin conditions, such as atopic dermatitis.
Chemokine CCL4, also known as macrophage inflammatory protein 1β (MIP-1β), is a small protein that plays a role in the immune system. It is a type of chemokine, which are a group of signaling molecules that help to direct the movement of immune cells to specific areas of the body in response to infection or injury. CCL4 is produced by a variety of cells, including macrophages, monocytes, and T cells. It is involved in the recruitment of immune cells to sites of inflammation and is also thought to play a role in the development of certain types of cancer. In the medical field, CCL4 is often studied as a potential target for the treatment of diseases such as cancer, autoimmune disorders, and viral infections. It is also used as a diagnostic marker for certain conditions, such as HIV infection and liver disease.
Chemokine CXCL12, also known as stromal cell-derived factor-1 (SDF-1), is a small protein that plays a crucial role in the recruitment and migration of immune cells to specific areas of the body. It is a member of the chemokine family of proteins, which are responsible for directing the movement of cells in response to chemical signals. CXCL12 is primarily produced by cells in the bone marrow, liver, and other tissues, and it is released in response to various stimuli, including inflammation, injury, and infection. It acts by binding to specific receptors on the surface of immune cells, such as T cells, B cells, and monocytes, and guiding them to the site of injury or infection. CXCL12 is also involved in the development and maintenance of the immune system, as well as in the regulation of angiogenesis (the formation of new blood vessels). It has been implicated in a variety of diseases, including cancer, autoimmune disorders, and infectious diseases, and it is a target for the development of new therapies.
Receptors, CCR1 are a type of cell surface receptor protein that belongs to the CC chemokine receptor family. These receptors are expressed on various immune cells, including monocytes, macrophages, and T cells, and play a role in the recruitment and activation of these cells in response to inflammatory stimuli. The CCR1 receptor is activated by certain chemokines, which are small signaling molecules that help to regulate the movement of immune cells within the body. When activated, CCR1 receptors can trigger a variety of cellular responses, including the production of inflammatory cytokines, the migration of immune cells to sites of inflammation, and the activation of immune cell signaling pathways. In the medical field, the CCR1 receptor is of interest because it has been implicated in a number of inflammatory and immune-related diseases, including asthma, multiple sclerosis, and rheumatoid arthritis. In some cases, drugs that target the CCR1 receptor have been developed as potential treatments for these conditions.
Chemokine CXCL10, also known as interferon-gamma-inducible protein 10 (IP-10), is a small protein that plays a role in the immune system. It is produced by various cells in response to infection, inflammation, or other stimuli, and it functions as a chemoattractant, recruiting immune cells to the site of infection or injury. CXCL10 is a member of the CXC chemokine family, which is a group of proteins that are involved in the recruitment and activation of immune cells. It is particularly important in the immune response to viral infections, as it helps to recruit and activate T cells and natural killer (NK) cells, which are important for controlling viral infections. In addition to its role in the immune response, CXCL10 has been implicated in a number of other physiological processes, including angiogenesis (the formation of new blood vessels), tissue repair, and the regulation of inflammation. It has also been studied in the context of various diseases, including cancer, autoimmune disorders, and infectious diseases.
Chemokine CCL8, also known as macrophage inflammatory protein 1 alpha (MIP-1α), is a small protein that plays a role in the immune system. It is a type of chemokine, which are proteins that help to direct the movement of immune cells to specific areas of the body in response to infection or injury. CCL8 is produced by a variety of cells, including macrophages, monocytes, and endothelial cells, in response to inflammatory stimuli. It functions by binding to specific receptors on the surface of immune cells, such as T cells and monocytes, and guiding them to the site of inflammation. CCL8 has been implicated in a number of different diseases and conditions, including asthma, chronic obstructive pulmonary disease (COPD), and certain types of cancer. It is also involved in the recruitment of immune cells to the site of infection or injury, and plays a role in the development of inflammation and tissue damage. Overall, CCL8 is an important molecule in the immune system that helps to regulate the movement of immune cells and contribute to the body's response to infection and injury.
Receptors, CCR (Chemokine Receptors, CCR) are a family of cell surface receptors that are involved in the immune system's response to infection and inflammation. They are activated by chemokines, which are small signaling molecules that help to direct immune cells to specific areas of the body where they are needed. There are several different subtypes of CCR receptors, each of which is activated by a specific chemokine. These receptors are found on a variety of immune cells, including T cells, B cells, macrophages, and dendritic cells. When a chemokine binds to its specific receptor, it triggers a signaling cascade within the cell that leads to changes in cell behavior, such as migration, proliferation, or activation. The CCR receptors play an important role in the immune response to infection and inflammation, and they are also involved in the development of certain diseases, such as cancer and autoimmune disorders. Understanding the function of these receptors is important for developing new treatments for these conditions.
Receptors, CCR2 are a type of cell surface receptors that are expressed on various immune cells, including monocytes, macrophages, and dendritic cells. These receptors are activated by a chemokine called CCL2 (also known as MCP-1), which is produced by various cells in response to inflammation or injury. When CCR2 receptors are activated by CCL2, they trigger a signaling cascade within the cell that leads to the recruitment and activation of immune cells to the site of inflammation or injury. This process is important for the body's immune response to infections, tissue damage, and other types of stress. However, excessive activation of CCR2 receptors and the chemokine CCL2 has been implicated in the development of various inflammatory and autoimmune diseases, such as atherosclerosis, rheumatoid arthritis, and multiple sclerosis. Therefore, targeting CCR2 receptors has become an area of active research for the development of new therapies for these diseases.
Chemokine CCL11, also known as eotaxin-1, is a type of protein that plays a role in the immune system. It is a chemokine, which is a type of signaling molecule that helps to direct the movement of immune cells to specific areas of the body in response to infection or injury. CCL11 is primarily produced by cells in the lung and is involved in the recruitment of eosinophils, a type of white blood cell, to the lung. Eosinophils play a role in the immune response to parasitic infections and in allergic reactions, such as asthma. CCL11 is also involved in the recruitment of other immune cells, such as T cells and monocytes, to the lung. In the medical field, CCL11 is often studied in the context of asthma and other allergic diseases, as well as in the development of new treatments for these conditions. It is also being studied as a potential target for cancer therapy, as it has been found to be overexpressed in some types of cancer.
Chemokine CCL24, also known as eotaxin-2, is a type of protein that plays a role in the immune system. It is a chemokine, which means that it is a signaling molecule that helps to direct the movement of immune cells, such as eosinophils, to specific areas of the body where they are needed. Eotaxin-2 is primarily produced by cells in the skin, lungs, and other tissues, and it is thought to play a role in the recruitment of eosinophils to these areas in response to inflammation or allergic reactions. Eosinophils are a type of white blood cell that are involved in the immune response to parasites and allergens, and they are also involved in the development of certain types of asthma and other inflammatory diseases. In the medical field, chemokine CCL24 is sometimes used as a diagnostic marker for certain conditions, such as asthma and other allergic diseases, and it is also being studied as a potential therapeutic target for the treatment of these conditions.
Receptors, CCR7 are a type of cell surface receptor protein that are expressed on the surface of certain immune cells, such as T cells and dendritic cells. These receptors are activated by a chemical messenger called chemokine (C-C motif) ligand 19 (CCL19) and chemokine (C-C motif) ligand 21 (CCL21), which are produced by cells in the lymphatic system and the spleen. When CCR7 receptors are activated by CCL19 or CCL21, they trigger a signaling cascade within the immune cell that promotes its movement towards the site of infection or inflammation. This process, known as chemotaxis, is an important mechanism for the recruitment of immune cells to the site of an infection or injury. In addition to their role in immune cell trafficking, CCR7 receptors have also been implicated in the development and progression of certain types of cancer, such as breast cancer and non-small cell lung cancer. In these cases, the overexpression of CCR7 receptors on cancer cells can promote their migration and spread to other parts of the body, making them more difficult to treat.
Receptors, CCR8 are a type of cell surface receptors that are expressed on various immune cells, including T cells, B cells, and dendritic cells. These receptors are activated by the chemokine CCL1, also known as eotaxin-1, which is produced by various cells in the body, including epithelial cells, fibroblasts, and mast cells. The activation of CCR8 receptors by CCL1 has been shown to play a role in the recruitment and activation of immune cells, particularly eosinophils, to sites of inflammation. This is important in the context of allergic reactions, where eosinophils are involved in the release of inflammatory mediators that contribute to symptoms such as itching, swelling, and airway constriction. In addition to their role in allergic reactions, CCR8 receptors have also been implicated in the pathogenesis of other inflammatory diseases, such as rheumatoid arthritis and multiple sclerosis. Therefore, targeting CCR8 receptors may be a potential therapeutic strategy for the treatment of these conditions.
Chemokine CXCL1, also known as Interleukin-8 (IL-8), is a type of protein that plays a crucial role in the immune system. It is a chemokine, which means that it is a type of signaling molecule that attracts immune cells to specific areas of the body in response to infection or injury. CXCL1 is produced by a variety of cells, including immune cells such as neutrophils, monocytes, and macrophages, as well as epithelial cells and fibroblasts. It is primarily involved in the recruitment of neutrophils to sites of inflammation, where they help to fight off infection and clear damaged tissue. In addition to its role in inflammation, CXCL1 has been implicated in a number of other biological processes, including cancer progression, angiogenesis (the formation of new blood vessels), and tissue repair. It is also a potential therapeutic target for the treatment of a variety of diseases, including cancer, autoimmune disorders, and inflammatory conditions.
Chemotaxis, leukocyte refers to the movement of white blood cells (leukocytes) in response to chemical signals in the body. These chemical signals, also known as chemokines, are released by damaged or infected cells, as well as by immune cells themselves. Chemotaxis allows leukocytes to move towards the site of inflammation or infection, where they can help to fight off pathogens and promote tissue repair. This process is an important part of the immune response and plays a critical role in maintaining overall health and wellbeing.
Receptors, CCR4, are a type of cell surface receptor that belongs to the CC chemokine receptor family. These receptors are expressed on various immune cells, including T cells, eosinophils, and basophils, and play a role in the recruitment and activation of these cells in response to certain chemokines. The CCR4 receptor is activated by chemokines such as CCL17 and CCL22, which are produced by various cells in the body, including immune cells and epithelial cells. Activation of CCR4 receptors on immune cells leads to their migration to sites of inflammation or infection, where they can help to fight off pathogens or clear damaged tissue. In addition to their role in immune cell recruitment and activation, CCR4 receptors have also been implicated in various diseases, including asthma, allergies, and certain types of cancer. For example, high levels of CCR4 expression on T cells have been associated with poor prognosis in patients with certain types of leukemia and lymphoma.
Chemokines, CXC are a family of small proteins that play a crucial role in the immune system. They are secreted by various cells in response to infection, injury, or inflammation and act as chemoattractants to recruit immune cells to the site of injury or infection. CXC chemokines are characterized by the presence of a conserved cysteine (C) at the first position and a glutamine (Q) or glutamic acid (E) at the second position in their amino acid sequence. They are classified into four subfamilies based on the position of the second cysteine residue: CX3C, CXCL, CXCL1, and CXCL2. CXC chemokines play a critical role in the recruitment and activation of immune cells, including neutrophils, monocytes, and lymphocytes, to the site of infection or injury. They also play a role in the development of chronic inflammatory diseases, such as asthma, rheumatoid arthritis, and atherosclerosis. In the medical field, CXC chemokines are used as diagnostic markers for various diseases, including cancer, infectious diseases, and autoimmune disorders. They are also being investigated as potential therapeutic targets for the treatment of these diseases.
Chemokine CX3CL1, also known as fractalkine, is a type of chemokine that plays a role in the recruitment and migration of immune cells to sites of inflammation or infection. It is expressed on the surface of various cell types, including endothelial cells, neurons, and microglia, and is involved in the regulation of immune cell trafficking and tissue repair. CX3CL1 binds to its receptor, CX3CR1, which is expressed on the surface of immune cells such as monocytes, macrophages, and T cells. Activation of CX3CR1 by CX3CL1 has been shown to promote the migration of immune cells towards the site of inflammation, as well as to modulate immune cell function and contribute to the resolution of inflammation. In addition, CX3CL1 has been implicated in various diseases, including neurodegenerative disorders, cardiovascular disease, and cancer.
Macrophage Inflammatory Proteins (MIPs) are a family of small proteins that are produced by macrophages, a type of white blood cell. These proteins play a role in the immune response by promoting inflammation and attracting other immune cells to the site of infection or injury. MIPs are also involved in the regulation of angiogenesis, the formation of new blood vessels, and in the development of certain types of cancer. There are several different types of MIPs, including MIP-1α, MIP-1β, and MIP-2, each with its own specific functions and effects on the immune system.
Receptors, CCR5, are a type of cell surface receptor protein that are expressed on the surface of certain immune cells, such as T cells and macrophages. These receptors are part of the chemokine receptor family and are activated by certain chemokines, which are signaling molecules that help to regulate the movement and function of immune cells. The CCR5 receptor plays an important role in the immune response to HIV (human immunodeficiency virus), which targets and destroys CD4+ T cells, a type of immune cell that expresses CCR5 on its surface. HIV uses the CCR5 receptor to enter and infect these cells. As a result, individuals who lack functional CCR5 receptors (due to a genetic mutation) are resistant to HIV infection. In addition to its role in HIV infection, the CCR5 receptor has been implicated in a variety of other immune-related disorders, including multiple sclerosis, rheumatoid arthritis, and inflammatory bowel disease. As such, the CCR5 receptor is an important target for the development of new therapies for these conditions.
Receptors, CCR3 are a type of cell surface receptor that belongs to the chemokine receptor family. They are primarily expressed on immune cells, such as eosinophils, basophils, and mast cells, and play a role in the recruitment and activation of these cells in response to certain chemical signals, such as chemokines. CCR3 receptors are involved in a variety of physiological processes, including inflammation, allergic responses, and the immune response to parasites. They are also implicated in the development of certain diseases, such as asthma, chronic obstructive pulmonary disease (COPD), and certain types of cancer. In the medical field, CCR3 receptors are often targeted in the development of new drugs for the treatment of these conditions. For example, drugs that block CCR3 receptors can help to reduce inflammation and allergic responses, and may be useful in the treatment of asthma and COPD.
Chemokine CXCL9, also known as interferon-inducible protein 10 (IP-10), is a small protein that plays a role in the immune response. It is a type of chemokine, which are proteins that help to direct the movement of immune cells to specific areas of the body where they are needed. CXCL9 is produced by a variety of cells, including immune cells such as T cells and macrophages, in response to the presence of certain stimuli, such as viral infections or inflammatory signals. It functions by binding to specific receptors on the surface of immune cells, which triggers a signaling cascade that leads to the activation and recruitment of these cells to the site of inflammation. In the context of medical research, CXCL9 has been studied for its potential role in a variety of conditions, including viral infections, autoimmune diseases, and cancer. For example, high levels of CXCL9 have been associated with the progression of certain types of cancer, and it has been proposed as a potential target for the development of new cancer therapies.
In the medical field, cell movement refers to the ability of cells to move from one location to another within a tissue or organism. This movement can occur through various mechanisms, including crawling, rolling, and sliding, and is essential for many physiological processes, such as tissue repair, immune response, and embryonic development. There are several types of cell movement, including: 1. Chemotaxis: This is the movement of cells in response to chemical gradients, such as the concentration of a signaling molecule. 2. Haptotaxis: This is the movement of cells in response to physical gradients, such as the stiffness or topography of a substrate. 3. Random walk: This is the movement of cells in a seemingly random manner, which can be influenced by factors such as cell adhesion and cytoskeletal dynamics. 4. Amoeboid movement: This is the movement of cells that lack a well-defined cytoskeleton and rely on changes in cell shape and adhesion to move. Understanding cell movement is important for many medical applications, including the development of new therapies for diseases such as cancer, the study of tissue regeneration and repair, and the design of new materials for tissue engineering and regenerative medicine.
Chemokine CXCL2, also known as neutrophil chemotactic factor 2 (NCF2) or macrophage inflammatory protein 2 (MIP-2), is a small protein that plays a crucial role in the immune response. It is a member of the CXC chemokine family, which is a group of proteins that regulate the movement of immune cells, such as neutrophils and macrophages, to sites of inflammation or infection. CXCL2 is produced by a variety of cells, including monocytes, macrophages, and endothelial cells, in response to inflammatory stimuli such as bacterial or viral infections, tissue damage, or injury. It acts as a chemoattractant, drawing immune cells to the site of inflammation by binding to specific receptors on their surface. Once CXCL2 binds to its receptors, it triggers a signaling cascade that leads to the activation and migration of immune cells towards the site of inflammation. This process is essential for the clearance of pathogens and the resolution of inflammation. In addition to its role in the immune response, CXCL2 has been implicated in a variety of other physiological processes, including wound healing, angiogenesis, and cancer progression.
Chemokine CXCL13, also known as B lymphocyte chemoattractant 1 (BCA-1) or B cell-attracting chemokine 1 (BCA-1), is a type of chemokine that plays a crucial role in the immune system. It is primarily produced by stromal cells, such as follicular dendritic cells and astrocytes, and is involved in the recruitment and retention of B cells in the lymphoid follicles of secondary lymphoid organs, such as the lymph nodes and spleen. CXCL13 is a potent chemoattractant for B cells, and it is believed to play a key role in the formation and maintenance of the germinal centers within lymphoid follicles. These centers are sites of intense B cell proliferation and differentiation, where B cells undergo somatic hypermutation and affinity maturation to generate high-affinity antibodies. In addition to its role in B cell biology, CXCL13 has also been implicated in the pathogenesis of several autoimmune diseases, such as systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA), as well as in the development of certain types of cancer, such as non-Hodgkin's lymphoma (NHL) and multiple myeloma (MM).
Receptors, CXCR4 are a type of protein found on the surface of certain cells in the human body. These proteins are known as chemokine receptors, and they play a role in regulating the movement of cells within the body. Specifically, CXCR4 receptors are activated by a chemical messenger called CXCL12, which is produced by cells in various tissues throughout the body. When CXCR4 receptors are activated by CXCL12, they trigger a signaling cascade within the cell that can lead to a variety of cellular responses, including changes in cell migration, proliferation, and survival. In the medical field, CXCR4 receptors and their interactions with CXCL12 are of interest because they have been implicated in a number of different diseases and conditions, including cancer, HIV infection, and cardiovascular disease.
Chemokine CXCL11, also known as interferon-inducible protein 10 (IP-10) or lymphotactin, is a small protein that plays a role in the immune system. It is a type of chemokine, which are proteins that help to direct the movement of immune cells to specific areas of the body in response to infection or injury. CXCL11 is produced by a variety of cells, including immune cells such as T cells, natural killer cells, and macrophages, as well as endothelial cells and fibroblasts. It is induced by a variety of stimuli, including interferon-gamma (IFN-gamma), interleukin-12 (IL-12), and lipopolysaccharide (LPS). CXCL11 functions by binding to specific receptors on the surface of immune cells, such as CXCR3, which is expressed on T cells, natural killer cells, and other immune cells. This binding causes the cells to change shape and move towards the source of the chemokine, allowing them to migrate to areas of the body where they are needed to fight infection or injury. In the medical field, CXCL11 is often studied in the context of various diseases and conditions, including infectious diseases, autoimmune diseases, and cancer. For example, CXCL11 has been shown to play a role in the recruitment of immune cells to the site of infection, and it has been implicated in the development of certain types of cancer, such as lung cancer and melanoma. It is also being investigated as a potential therapeutic target for the treatment of these diseases.
Chemotaxis is a process by which cells move in response to chemical gradients. In the medical field, chemotaxis is an important mechanism that cells use to migrate to specific locations in the body in response to chemical signals. For example, immune cells such as neutrophils and macrophages use chemotaxis to migrate to sites of infection or inflammation. In this way, chemotaxis plays a critical role in the body's immune response.
Chemokine CXCL6, also known as fractalkine, is a type of chemokine protein that plays a role in the immune system. It is expressed by a variety of cell types, including endothelial cells, smooth muscle cells, and macrophages, and is involved in the recruitment and activation of immune cells, such as neutrophils and monocytes, to sites of inflammation or injury. CXCL6 is a chemotactic factor, meaning that it attracts immune cells to specific locations in the body. It is also involved in the regulation of angiogenesis, the formation of new blood vessels, and has been implicated in the development of various diseases, including atherosclerosis, cancer, and inflammatory bowel disease. In the medical field, CXCL6 is often studied as a potential therapeutic target for the treatment of various diseases, as well as a biomarker for disease progression or response to treatment.
In the medical field, "Cells, Cultured" refers to cells that have been grown and maintained in a controlled environment outside of their natural biological context, typically in a laboratory setting. This process is known as cell culture and involves the isolation of cells from a tissue or organism, followed by their growth and proliferation in a nutrient-rich medium. Cultured cells can be derived from a variety of sources, including human or animal tissues, and can be used for a wide range of applications in medicine and research. For example, cultured cells can be used to study the behavior and function of specific cell types, to develop new drugs and therapies, and to test the safety and efficacy of medical products. Cultured cells can be grown in various types of containers, such as flasks or Petri dishes, and can be maintained at different temperatures and humidity levels to optimize their growth and survival. The medium used to culture cells typically contains a combination of nutrients, growth factors, and other substances that support cell growth and proliferation. Overall, the use of cultured cells has revolutionized medical research and has led to many important discoveries and advancements in the field of medicine.
Dendritic cells are a type of immune cell that plays a crucial role in the body's immune response. They are found in various tissues throughout the body, including the skin, lymph nodes, and mucous membranes. Dendritic cells are responsible for capturing and processing antigens, which are foreign substances that can trigger an immune response. They do this by engulfing and breaking down antigens, and then presenting them to other immune cells, such as T cells, in a way that activates the immune response. Dendritic cells are also involved in the regulation of immune responses, helping to prevent the body from overreacting to harmless substances and to maintain immune tolerance to self-antigens. In the medical field, dendritic cells are being studied for their potential use in cancer immunotherapy. They can be genetically modified to recognize and attack cancer cells, and are being tested in clinical trials as a way to treat various types of cancer.
Chemokine CXCL5, also known as interleukin-8 (IL-8), is a type of protein that plays a role in the immune system. It is a chemokine, which means that it is a type of signaling molecule that helps to direct the movement of immune cells to specific areas of the body where they are needed. CXCL5 is produced by a variety of cells, including immune cells such as neutrophils, monocytes, and macrophages, as well as epithelial cells and fibroblasts. It is involved in the recruitment of immune cells to sites of inflammation or infection, and it has been implicated in a number of different diseases, including cancer, chronic obstructive pulmonary disease (COPD), and inflammatory bowel disease (IBD). In the medical field, CXCL5 is often measured in blood or other bodily fluids as a way to assess the activity of the immune system and to monitor the progression of certain diseases. It is also being studied as a potential therapeutic target for the treatment of a variety of conditions, including cancer and inflammatory diseases.
Cytokines are small proteins that are produced by various cells of the immune system, including white blood cells, macrophages, and dendritic cells. They play a crucial role in regulating immune responses and inflammation, and are involved in a wide range of physiological processes, including cell growth, differentiation, and apoptosis. Cytokines can be classified into different groups based on their function, including pro-inflammatory cytokines, anti-inflammatory cytokines, and regulatory cytokines. Pro-inflammatory cytokines, such as tumor necrosis factor-alpha (TNF-alpha) and interleukin-1 (IL-1), promote inflammation and recruit immune cells to the site of infection or injury. Anti-inflammatory cytokines, such as interleukin-10 (IL-10) and transforming growth factor-beta (TGF-beta), help to dampen the immune response and prevent excessive inflammation. Regulatory cytokines, such as interleukin-4 (IL-4) and interleukin-13 (IL-13), help to regulate the balance between pro-inflammatory and anti-inflammatory responses. Cytokines play a critical role in many diseases, including autoimmune disorders, cancer, and infectious diseases. They are also important in the development of vaccines and immunotherapies.
Receptors, CXCR3 are a type of protein receptors found on the surface of certain cells in the immune system. They are activated by a chemical messenger called CXCL10, which is produced by immune cells in response to infection or inflammation. Activation of CXCR3 receptors triggers a signaling cascade within the cell that leads to the recruitment and activation of immune cells, such as T cells and natural killer cells, to the site of infection or inflammation. CXCR3 receptors play a critical role in the immune response to viral infections, such as HIV and influenza, and in the development of certain autoimmune diseases, such as multiple sclerosis and rheumatoid arthritis.
In the medical field, RNA, Messenger (mRNA) refers to a type of RNA molecule that carries genetic information from DNA in the nucleus of a cell to the ribosomes, where proteins are synthesized. During the process of transcription, the DNA sequence of a gene is copied into a complementary RNA sequence called messenger RNA (mRNA). This mRNA molecule then leaves the nucleus and travels to the cytoplasm of the cell, where it binds to ribosomes and serves as a template for the synthesis of a specific protein. The sequence of nucleotides in the mRNA molecule determines the sequence of amino acids in the protein that is synthesized. Therefore, changes in the sequence of nucleotides in the mRNA molecule can result in changes in the amino acid sequence of the protein, which can affect the function of the protein and potentially lead to disease. mRNA molecules are often used in medical research and therapy as a way to introduce new genetic information into cells. For example, mRNA vaccines work by introducing a small piece of mRNA that encodes for a specific protein, which triggers an immune response in the body.
Inflammation is a complex biological response of the body to harmful stimuli, such as pathogens, damaged cells, or irritants. It is a protective mechanism that helps to eliminate the cause of injury, remove damaged tissue, and initiate the healing process. Inflammation involves the activation of immune cells, such as white blood cells, and the release of chemical mediators, such as cytokines and prostaglandins. This leads to the characteristic signs and symptoms of inflammation, including redness, heat, swelling, pain, and loss of function. Inflammation can be acute or chronic. Acute inflammation is a short-term response that lasts for a few days to a few weeks and is usually beneficial. Chronic inflammation, on the other hand, is a prolonged response that lasts for months or years and can be harmful if it persists. Chronic inflammation is associated with many diseases, including cancer, cardiovascular disease, and autoimmune disorders.
Receptors, Interleukin-8B (IL-8B) are a type of protein receptor found on the surface of certain cells in the immune system. These receptors are activated by the binding of interleukin-8B (IL-8B), a type of cytokine, which is a signaling molecule that plays a role in regulating immune responses. IL-8B receptors are primarily expressed on neutrophils, a type of white blood cell that plays a key role in the body's defense against infection. When IL-8B binds to its receptor on a neutrophil, it triggers a signaling cascade that leads to the activation and recruitment of the neutrophil to the site of infection or inflammation. IL-8B receptors are also expressed on other immune cells, including monocytes, macrophages, and T cells, although to a lesser extent. Activation of these receptors on these cells can also contribute to immune responses, although the specific effects depend on the cell type and the context in which the receptors are activated. Overall, IL-8B receptors play an important role in regulating immune responses and are a key target for the development of therapies for a variety of inflammatory and infectious diseases.
Atopic dermatitis, also known as eczema, is a chronic inflammatory skin condition characterized by dry, itchy, and red skin. It is a common condition that affects both children and adults, and is often associated with a family history of allergies and asthma. The exact cause of atopic dermatitis is not fully understood, but it is believed to involve a combination of genetic and environmental factors. The condition is thought to be caused by an overactive immune system response to irritants or allergens in the environment, which leads to inflammation and dryness of the skin. Symptoms of atopic dermatitis can include red, itchy, and dry skin, which may be covered with scales or crusts. The condition can be very uncomfortable and can lead to sleep disturbances and other quality-of-life issues. It is often treated with moisturizers, corticosteroid creams, and other medications to help reduce inflammation and itching. In some cases, immunosuppressive medications may be prescribed to help control the condition.
In the medical field, a cell line refers to a group of cells that have been derived from a single parent cell and have the ability to divide and grow indefinitely in culture. These cells are typically grown in a laboratory setting and are used for research purposes, such as studying the effects of drugs or investigating the underlying mechanisms of diseases. Cell lines are often derived from cancerous cells, as these cells tend to divide and grow more rapidly than normal cells. However, they can also be derived from normal cells, such as fibroblasts or epithelial cells. Cell lines are characterized by their unique genetic makeup, which can be used to identify them and compare them to other cell lines. Because cell lines can be grown in large quantities and are relatively easy to maintain, they are a valuable tool in medical research. They allow researchers to study the effects of drugs and other treatments on specific cell types, and to investigate the underlying mechanisms of diseases at the cellular level.
Monocyte chemoattractant proteins (MCPs) are a family of small proteins that are produced by various cells in the body, including immune cells, endothelial cells, and fibroblasts. These proteins play a crucial role in the recruitment of monocytes, a type of white blood cell, to sites of inflammation or injury. MCPs function by binding to specific receptors on the surface of monocytes, which triggers a signaling cascade that leads to the activation and migration of these cells towards the site of inflammation. This process is known as chemotaxis. There are several different types of MCPs, including MCP-1, MCP-2, MCP-3, MCP-4, and MCP-5, each with its own specific properties and functions. MCPs are also involved in other physiological processes, such as the regulation of angiogenesis (the formation of new blood vessels) and the development of atherosclerosis (the buildup of plaque in the arteries). In the medical field, MCPs are often studied as potential biomarkers for various diseases, including inflammatory disorders, cardiovascular disease, and cancer. They are also being investigated as potential therapeutic targets for the treatment of these conditions.
In the medical field, "Disease Models, Animal" refers to the use of animals to study and understand human diseases. These models are created by introducing a disease or condition into an animal, either naturally or through experimental manipulation, in order to study its progression, symptoms, and potential treatments. Animal models are used in medical research because they allow scientists to study diseases in a controlled environment and to test potential treatments before they are tested in humans. They can also provide insights into the underlying mechanisms of a disease and help to identify new therapeutic targets. There are many different types of animal models used in medical research, including mice, rats, rabbits, dogs, and monkeys. Each type of animal has its own advantages and disadvantages, and the choice of model depends on the specific disease being studied and the research question being addressed.
Interleukin-8 (IL-8) is a type of cytokine, which is a signaling molecule that plays a role in regulating the immune system. It is produced by various types of cells, including immune cells such as neutrophils, monocytes, and macrophages, as well as epithelial cells and fibroblasts. IL-8 is primarily involved in the recruitment and activation of neutrophils, which are a type of white blood cell that plays a key role in the body's defense against infection and inflammation. IL-8 binds to receptors on the surface of neutrophils, causing them to migrate to the site of infection or inflammation. It also promotes the production of other pro-inflammatory molecules by neutrophils, which helps to amplify the immune response. IL-8 has been implicated in a variety of inflammatory and autoimmune diseases, including chronic obstructive pulmonary disease (COPD), asthma, rheumatoid arthritis, and inflammatory bowel disease. It is also involved in the development of certain types of cancer, such as lung cancer and ovarian cancer. In the medical field, IL-8 is often measured in blood or other bodily fluids as a marker of inflammation or immune activation. It is also being studied as a potential therapeutic target for the treatment of various diseases, including cancer and inflammatory disorders.
Receptors, CCR6 are a type of cell surface receptors that are expressed on certain immune cells, such as T cells and dendritic cells. These receptors are activated by a chemical messenger called CCL20, which is produced by cells in the body in response to infection or inflammation. CCR6 receptors play a role in the recruitment and activation of immune cells to sites of infection or inflammation. They are also involved in the development and function of certain types of immune cells, such as Th17 cells, which are important for fighting off certain types of infections. Abnormalities in the function or expression of CCR6 receptors have been linked to a number of diseases, including autoimmune disorders, allergies, and certain types of cancer. For example, some studies have suggested that CCR6 receptors may play a role in the development of multiple sclerosis, a chronic autoimmune disorder that affects the central nervous system.
CD4-positive T-lymphocytes, also known as CD4+ T-cells or T-helper cells, are a type of white blood cell that plays a critical role in the immune system. They are a subset of T-cells that express the CD4 protein on their surface, which allows them to recognize and bind to antigens presented by other immune cells. CD4+ T-cells are involved in many aspects of the immune response, including the activation and proliferation of other immune cells, the production of cytokines (chemical messengers that regulate immune responses), and the regulation of immune tolerance. They are particularly important in the response to infections caused by viruses, such as HIV, and in the development of autoimmune diseases. In HIV infection, the virus specifically targets and destroys CD4+ T-cells, leading to a decline in their numbers and a weakened immune system. This is why CD4+ T-cell count is an important marker of HIV disease progression and treatment response.
Receptors, Interleukin-8A, also known as CXCR1 and CXCR2, are a type of protein receptor found on the surface of certain cells in the immune system. These receptors are activated by a signaling molecule called interleukin-8 (IL-8), which is produced by immune cells in response to infection or injury. IL-8 plays an important role in the body's immune response by recruiting immune cells to the site of infection or injury. When IL-8 binds to its receptors on immune cells, it triggers a signaling cascade that leads to the activation and migration of these cells to the site of inflammation. Receptors, Interleukin-8A are expressed on a variety of immune cells, including neutrophils, monocytes, and macrophages. They are also found on some non-immune cells, such as epithelial cells and fibroblasts. Abnormalities in the function or expression of these receptors have been linked to a number of diseases, including inflammatory disorders, cancer, and cardiovascular disease. For example, mutations in the gene that encodes for CXCR1 or CXCR2 can lead to a condition called chronic neutrophilic leukemia, which is characterized by an overproduction of neutrophils.
Receptors, CXCR refer to a family of G protein-coupled receptors (GPCRs) that are activated by chemokines, a type of signaling molecule that plays a crucial role in immune cell trafficking and inflammation. The CXCR receptors are expressed on the surface of various immune cells, including T cells, B cells, and natural killer cells, and are involved in the recruitment and activation of these cells in response to infection or injury. There are several different CXCR receptors, including CXCR1, CXCR2, CXCR3, CXCR4, and CXCR5, each of which is activated by a specific subset of chemokines. Activation of these receptors leads to the activation of intracellular signaling pathways that regulate various cellular processes, including cell migration, proliferation, and differentiation. Abnormalities in the function or expression of CXCR receptors have been implicated in a variety of diseases, including cancer, autoimmune disorders, and infectious diseases. As such, the CXCR receptors are an important target for the development of new therapeutic agents for the treatment of these conditions.
A cell line, tumor is a type of cell culture that is derived from a cancerous tumor. These cell lines are grown in a laboratory setting and are used for research purposes, such as studying the biology of cancer and testing potential new treatments. They are typically immortalized, meaning that they can continue to divide and grow indefinitely, and they often exhibit the characteristics of the original tumor from which they were derived, such as specific genetic mutations or protein expression patterns. Cell lines, tumor are an important tool in cancer research and have been used to develop many of the treatments that are currently available for cancer patients.
NF-kappa B (Nuclear Factor kappa B) is a transcription factor that plays a critical role in regulating the immune response, inflammation, and cell survival. It is a complex of proteins that is found in the cytoplasm of cells and is activated in response to various stimuli, such as cytokines, bacterial and viral infections, and stress. When activated, NF-kappa B translocates to the nucleus and binds to specific DNA sequences, promoting the expression of genes involved in immune and inflammatory responses. This includes genes encoding for cytokines, chemokines, and adhesion molecules, which help to recruit immune cells to the site of infection or injury. NF-kappa B is also involved in regulating cell survival and apoptosis (programmed cell death). Dysregulation of NF-kappa B signaling has been implicated in a variety of diseases, including cancer, autoimmune disorders, and inflammatory diseases such as rheumatoid arthritis and inflammatory bowel disease.
Carbon tetrachloride is a colorless, dense liquid with a sweet, chlorinated smell. It is a commonly used solvent in the medical field, particularly in the preparation of medications and in the sterilization of medical equipment. However, carbon tetrachloride is also a known neurotoxin and can cause serious health problems if inhaled or ingested in large quantities. It has been linked to liver damage, kidney damage, and even death in severe cases. As a result, its use in the medical field has been largely phased out in favor of safer alternatives.
Receptors, Cytokine are proteins that are present on the surface of cells and are responsible for binding to specific cytokines, which are signaling molecules that play a crucial role in regulating immune responses, cell growth, and differentiation. Cytokine receptors are typically found on the surface of immune cells, such as T cells and B cells, as well as on other cell types, such as endothelial cells and fibroblasts. When a cytokine binds to its specific receptor, it triggers a signaling cascade within the cell that can lead to a variety of cellular responses, such as the activation or suppression of immune cells, the promotion of cell growth or differentiation, or the regulation of inflammation. Dysregulation of cytokine signaling can contribute to a variety of diseases, including autoimmune disorders, cancer, and infectious diseases. Therefore, understanding the function and regulation of cytokine receptors is an important area of research in the medical field.
Tumor Necrosis Factor-alpha (TNF-alpha) is a cytokine, a type of signaling protein, that plays a crucial role in the immune response and inflammation. It is produced by various cells in the body, including macrophages, monocytes, and T cells, in response to infection, injury, or other stimuli. TNF-alpha has multiple functions in the body, including regulating the immune response, promoting cell growth and differentiation, and mediating inflammation. It can also induce programmed cell death, or apoptosis, in some cells, which can be beneficial in fighting cancer. However, excessive or prolonged TNF-alpha production can lead to chronic inflammation and tissue damage, which can contribute to the development of various diseases, including autoimmune disorders, inflammatory bowel disease, and certain types of cancer. In the medical field, TNF-alpha is often targeted in the treatment of these conditions. For example, drugs called TNF inhibitors, such as infliximab and adalimumab, are used to block the action of TNF-alpha and reduce inflammation in patients with rheumatoid arthritis, Crohn's disease, and other inflammatory conditions.
Chemokines, CX3C are a family of small proteins that play a crucial role in the immune system. They are chemotactic cytokines, meaning they attract immune cells to specific areas of the body in response to infection or injury. The CX3C chemokines are a subfamily of chemokines that are characterized by a conserved cysteine residue at the N-terminus and a cysteine residue at the C-terminus that forms a disulfide bond. The most well-known member of this subfamily is fractalkine (CX3CL1), which is expressed on the surface of endothelial cells, neurons, and other cell types. Fractalkine acts as a chemoattractant for immune cells, including monocytes, dendritic cells, and T cells, and plays a role in the recruitment of these cells to sites of inflammation. It also has anti-inflammatory properties and has been implicated in the regulation of immune cell trafficking and the development of autoimmune diseases. Overall, chemokines, CX3C are important mediators of immune cell trafficking and play a critical role in the immune response to infection and injury.
Receptors, CXCR5 are a type of protein receptors found on the surface of certain immune cells, such as T cells and B cells. These receptors are activated by a signaling molecule called CXCL13, which is produced by cells in the lymph nodes and other tissues. Activation of CXCR5 receptors helps to guide immune cells to the site of infection or inflammation, and plays a role in the development and maintenance of immune responses. Abnormalities in the function of CXCR5 receptors have been implicated in a number of autoimmune and inflammatory diseases, including lupus and rheumatoid arthritis.
Chemotactic factors are chemical substances that attract cells towards them. In the medical field, chemotactic factors play a crucial role in the immune response, where they help to direct immune cells to the site of infection or inflammation. Chemotactic factors are produced by various cells, including immune cells, endothelial cells, and fibroblasts. They can be proteins, peptides, or lipids, and they bind to specific receptors on the surface of immune cells, triggering a signaling cascade that leads to cell migration. Examples of chemotactic factors in the immune response include chemokines, which are a type of cytokine that attract immune cells such as neutrophils, monocytes, and lymphocytes to the site of infection or inflammation. Other examples include interleukins, growth factors, and complement proteins. Understanding the role of chemotactic factors in the immune response is important for developing new treatments for infectious diseases, autoimmune disorders, and cancer.
CD8-positive T-lymphocytes, also known as cytotoxic T-cells, are a type of white blood cell that plays a crucial role in the immune system's response to infections and diseases. These cells are a subtype of T-lymphocytes, which are a type of immune cell that plays a central role in cell-mediated immunity. CD8-positive T-lymphocytes are characterized by the presence of a protein called CD8 on their surface, which helps them to recognize and bind to infected cells or cancer cells. Once bound, these cells release toxic substances that can kill the infected or cancerous cells. CD8-positive T-lymphocytes are an important part of the immune system's response to viral infections, such as HIV and herpes, and to some types of cancer. They are also involved in the immune response to bacterial infections and in the regulation of immune responses to prevent autoimmune diseases. In the medical field, CD8-positive T-lymphocytes are often studied as a way to understand the immune system's response to infections and diseases, and to develop new treatments for these conditions.
Monokines are a type of cytokine, which are signaling molecules secreted by a single type of cell. Monokines are produced by various immune cells, such as macrophages, monocytes, and dendritic cells, in response to infection, inflammation, or other stimuli. They play a role in regulating immune responses, including the recruitment and activation of other immune cells, the production of antibodies, and the regulation of inflammation. Examples of monokines include interleukin-1 (IL-1), tumor necrosis factor-alpha (TNF-alpha), and interferon-gamma (IFN-gamma).
Receptors, HIV refers to the proteins on the surface of certain cells in the human immune system that are targeted by the human immunodeficiency virus (HIV). These receptors, known as CD4 receptors and chemokine receptors, play a crucial role in the entry and replication of HIV in the body. Once HIV binds to these receptors, it is able to enter the cell and use its genetic material to produce more copies of itself, leading to the destruction of immune cells and the progression of HIV infection to acquired immunodeficiency syndrome (AIDS).
Carbon tetrachloride poisoning is a medical condition that occurs when a person is exposed to high levels of carbon tetrachloride, a colorless, sweet-smelling liquid that was once commonly used as a solvent in various industrial and household products. The symptoms of carbon tetrachloride poisoning can vary depending on the level and duration of exposure, but they may include headache, dizziness, nausea, vomiting, abdominal pain, confusion, and difficulty breathing. In severe cases, carbon tetrachloride poisoning can lead to liver damage, kidney failure, and even death. The treatment for carbon tetrachloride poisoning typically involves supportive care, such as oxygen therapy, fluid replacement, and medications to manage symptoms. In some cases, activated charcoal may be given to help absorb the carbon tetrachloride from the body. Prevention of carbon tetrachloride poisoning involves avoiding exposure to the chemical, especially in its pure form, and using safer alternatives whenever possible. If you suspect that you or someone else may have been exposed to carbon tetrachloride, seek medical attention immediately.
Chemotactic factors, eosinophil are chemical substances that attract eosinophils, a type of white blood cell, to a specific location in the body. These factors are produced by various cells, including immune cells and cells in the lining of tissues, in response to inflammation or infection. Eosinophils play a role in the immune response to parasitic infections and allergies, and they are also involved in tissue repair and remodeling. Chemotactic factors for eosinophils can be either proteinaceous or lipid-based, and they bind to specific receptors on the surface of eosinophils, guiding them to the site of inflammation or infection.
Heterocyclic compounds are organic compounds that contain at least one ring composed of atoms other than carbon. In the medical field, heterocyclic compounds are often used as pharmaceuticals due to their ability to interact with biological targets and produce therapeutic effects. Examples of heterocyclic compounds used in medicine include: 1. Pyrimidines: These are a class of heterocyclic compounds that include thymine, cytosine, and uracil. They are important components of DNA and RNA and are used in the development of antiviral and anticancer drugs. 2. Purines: These are another class of heterocyclic compounds that include adenine and guanine. They are also important components of DNA and RNA and are used in the development of antiviral and anticancer drugs. 3. Imidazoles: These are heterocyclic compounds that contain a nitrogen atom and a carbon atom in a six-membered ring. They are used in the development of antifungal and anti-inflammatory drugs. 4. Quinolines: These are heterocyclic compounds that contain a nitrogen atom and two carbon atoms in a six-membered ring. They are used in the development of antimalarial and antituberculosis drugs. Overall, heterocyclic compounds play an important role in the development of new drugs and therapies in the medical field.
Interferon-gamma (IFN-γ) is a type of cytokine, which is a signaling molecule that plays a crucial role in the immune system. It is produced by various immune cells, including T cells, natural killer cells, and macrophages, in response to viral or bacterial infections, as well as in response to certain types of cancer. IFN-γ has a wide range of effects on the immune system, including the activation of macrophages and other immune cells, the inhibition of viral replication, and the promotion of T cell differentiation and proliferation. It also plays a role in the regulation of the immune response, helping to prevent excessive inflammation and tissue damage. In the medical field, IFN-γ is used as a therapeutic agent in the treatment of certain types of cancer, such as Hodgkin's lymphoma and multiple myeloma. It is also being studied as a potential treatment for other conditions, such as autoimmune diseases and viral infections.
Cell migration inhibition refers to the process of preventing or reducing the movement of cells from one location to another. In the medical field, this concept is often used to study the behavior of cells in various diseases and conditions, such as cancer, inflammation, and wound healing. Cell migration inhibition can be achieved through various mechanisms, including the use of chemical inhibitors, physical barriers, or changes in the extracellular matrix. For example, some drugs can block the activity of enzymes that are involved in cell migration, while others can interfere with the signaling pathways that regulate cell movement. In cancer research, cell migration inhibition is often used as a strategy to prevent the spread of cancer cells to other parts of the body, a process known as metastasis. By blocking cell migration, researchers hope to develop new treatments that can slow down or stop the progression of cancer. Overall, cell migration inhibition is an important concept in the medical field, as it can provide insights into the underlying mechanisms of various diseases and help to identify new therapeutic targets for treatment.
Intercellular signaling peptides and proteins are molecules that are secreted by cells and act as messengers to communicate with other cells. These molecules can be hormones, growth factors, cytokines, or other signaling molecules that are capable of transmitting information between cells. They play a crucial role in regulating various physiological processes, such as cell growth, differentiation, and apoptosis, as well as immune responses and inflammation. In the medical field, understanding the function and regulation of intercellular signaling peptides and proteins is important for developing new treatments for various diseases and disorders, including cancer, autoimmune diseases, and neurological disorders.
Lipopolysaccharides (LPS) are a type of complex carbohydrate found on the surface of gram-negative bacteria. They are composed of a lipid A moiety, a core polysaccharide, and an O-specific polysaccharide. LPS are important components of the bacterial cell wall and play a role in the innate immune response of the host. In the medical field, LPS are often studied in the context of sepsis, a life-threatening condition that occurs when the body's response to an infection causes widespread inflammation. LPS can trigger a strong immune response in the host, leading to the release of pro-inflammatory cytokines and other mediators that can cause tissue damage and organ failure. As a result, LPS are often used as a model for studying the pathophysiology of sepsis and for developing new treatments for this condition. LPS are also used in research as a tool for studying the immune system and for developing vaccines against bacterial infections. They can be purified from bacterial cultures and used to stimulate immune cells in vitro or in animal models, allowing researchers to study the mechanisms of immune responses to bacterial pathogens. Additionally, LPS can be used as an adjuvant in vaccines to enhance the immune response to the vaccine antigen.
In the medical field, an amino acid sequence refers to the linear order of amino acids in a protein molecule. Proteins are made up of chains of amino acids, and the specific sequence of these amino acids determines the protein's structure and function. The amino acid sequence is determined by the genetic code, which is a set of rules that specifies how the sequence of nucleotides in DNA is translated into the sequence of amino acids in a protein. Each amino acid is represented by a three-letter code, and the sequence of these codes is the amino acid sequence of the protein. The amino acid sequence is important because it determines the protein's three-dimensional structure, which in turn determines its function. Small changes in the amino acid sequence can have significant effects on the protein's structure and function, and this can lead to diseases or disorders. For example, mutations in the amino acid sequence of a protein involved in blood clotting can lead to bleeding disorders.
In the medical field, cell adhesion refers to the process by which cells stick to each other or to a surface. This is an essential process for the proper functioning of tissues and organs in the body. There are several types of cell adhesion, including: 1. Homophilic adhesion: This occurs when cells adhere to each other through the interaction of specific molecules on their surface. 2. Heterophilic adhesion: This occurs when cells adhere to each other through the interaction of different molecules on their surface. 3. Heterotypic adhesion: This occurs when cells adhere to each other through the interaction of different types of cells. 4. Intercellular adhesion: This occurs when cells adhere to each other through the interaction of molecules within the cell membrane. 5. Intracellular adhesion: This occurs when cells adhere to each other through the interaction of molecules within the cytoplasm. Cell adhesion is important for a variety of processes, including tissue development, wound healing, and the immune response. Disruptions in cell adhesion can lead to a variety of medical conditions, including cancer, autoimmune diseases, and inflammatory disorders.
Recombinant proteins are proteins that are produced by genetically engineering bacteria, yeast, or other organisms to express a specific gene. These proteins are typically used in medical research and drug development because they can be produced in large quantities and are often more pure and consistent than proteins that are extracted from natural sources. Recombinant proteins can be used for a variety of purposes in medicine, including as diagnostic tools, therapeutic agents, and research tools. For example, recombinant versions of human proteins such as insulin, growth hormones, and clotting factors are used to treat a variety of medical conditions. Recombinant proteins can also be used to study the function of specific genes and proteins, which can help researchers understand the underlying causes of diseases and develop new treatments.
Platelet Factor 4 (PF4) is a protein that is produced by platelets, which are small blood cells that play a crucial role in blood clotting. PF4 is a member of a family of proteins called chemokines, which are involved in the recruitment of immune cells to sites of injury or infection. PF4 is primarily known for its role in the immune response to bacterial infections. When bacteria enter the bloodstream, they can trigger the release of PF4 from platelets, which then binds to the bacteria and helps to recruit immune cells to the site of infection. PF4 also has anticoagulant properties, meaning that it can help to prevent blood clots from forming. In addition to its role in the immune response and blood clotting, PF4 has been implicated in a number of other medical conditions. For example, high levels of PF4 have been associated with certain autoimmune disorders, such as lupus and rheumatoid arthritis. PF4 has also been linked to the development of certain types of cancer, including lung cancer and ovarian cancer. Overall, PF4 is an important protein that plays a role in a variety of physiological processes, including immune response, blood clotting, and cancer development.
Bronchoalveolar Lavage Fluid (BALF) is a type of fluid that is collected from the airways and alveoli of the lungs. It is obtained by washing the airways and alveoli with a sterile saline solution using a bronchoscope, which is a thin, flexible tube that is inserted through the mouth or nose into the airways. BALF is used to diagnose and monitor a variety of lung diseases, including pneumonia, lung infections, lung cancer, and interstitial lung diseases. It can also be used to assess the immune response of the lungs and to detect the presence of foreign substances, such as bacteria, viruses, and fungi. The fluid is usually analyzed in a laboratory to determine the number and type of cells present, as well as the levels of various proteins and other substances. This information can help doctors to diagnose and treat the underlying cause of the patient's symptoms.
Drug-induced liver injury (DILI) is a type of liver damage that occurs as a result of taking medications or other substances. It can range from mild to severe and can be caused by a variety of drugs, including antibiotics, painkillers, and certain herbal supplements. DILI can present with a range of symptoms, including nausea, vomiting, abdominal pain, jaundice (yellowing of the skin and eyes), and dark urine. In severe cases, DILI can lead to liver failure, which can be life-threatening. Diagnosis of DILI typically involves a combination of clinical examination, laboratory tests, and imaging studies. Treatment may involve discontinuing the suspected drug, administering supportive care, and in severe cases, liver transplantation. Preventing DILI involves careful monitoring of patients who are taking medications that have the potential to cause liver damage, as well as educating patients about the potential risks and symptoms of DILI.
Coculture techniques refer to the process of growing two or more different cell types together in a single culture dish or flask. This is commonly used in the medical field to study interactions between cells, such as how cancer cells affect normal cells or how immune cells respond to pathogens. Coculture techniques can be used in a variety of ways, including co-culturing cells from different tissues or organs, co-culturing cells with different cell types, or co-culturing cells with microorganisms or other foreign substances. Coculture techniques can also be used to study the effects of drugs or other treatments on cell interactions. Overall, coculture techniques are a valuable tool in the medical field for studying cell interactions and developing new treatments for diseases.
Airway basal cell
Chemokine
Macrophage inflammatory protein
Duodenal-type follicular lymphoma
CC chemokine receptors
Microbial symbiosis and immunity
CCL4
Sperm chemotaxis
Sperm guidance
C-C motif chemokine ligand 27
DEFB103A
CCL20
LARC
CGAS-STING cytosolic DNA sensing pathway
T helper cell 22
Index of immunology articles
C-C chemokine receptor type 6
Mucosal-associated invariant T cell
CXCL9
Memory B cell
Interleukin 17
Stimulator of interferon genes
Th 9 cell
IL17A
Airway basal cell - Wikipedia
SMAD4 Suppresses Colitis-associated Carcinoma Through Inhibition of CCL20/CCR6-mediated Inflammation
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Publications by the founders of XLock Biosciences - XLock BIOSCIENCES
Receptor10
- Here, we examine the role of the chemokine/receptor pair CCL20/c-c motif chemokine receptor 6 (CCR6) in mediating colitis-associated colon carcinogenesis induced by SMAD4 loss. (nih.gov)
- Interferon pathway-related cytokines/chemokines, including interleukin (IL) 18, macrophage inflammatory protein 3α, and IL-33, were elevated, but tumor necrosis factor-α, IL-6, CXCL8 (formerly IL-8), and cytokines acting through C-C chemokine receptor 2 and CCR5 were lower among case-patients than controls. (cdc.gov)
- CCR6 is the sole receptor of CCL20. (zhihuiya.com)
- Lazucirnon (KST4290, ALK4290) is a small molecule, orally active inhibitor against CCR3, the natural receptor for chemokine eotaxin, decreases inflammatory cytokines in preclinical models. (probechem.com)
- And the expression of chemokine (C-C motif) ligand 20 (CCL20) and C-C chemokine receptor type 6 (CCR6) in converted cells were eval. (jrmds.in)
- A-SAA induced its own production and the synthesis of hBD2 and CCL20, both ligands for CCR6, a chemokine receptor involved in the trafficking of Th17 lymphocytes. (ox.ac.uk)
- However, potential associations between chemokine and chemokine receptor polymorphisms and BD have been fundamentally understudied. (psychiatryinvestigation.org)
- To identify participation of chemokines in BD pathogenesis, we examined genetic variants of several chemokine and chemokine receptor genes. (psychiatryinvestigation.org)
- Our findings indicate an association between genetic variants of certain chemokine and chemokine receptor (especially MCP-1) genes and BD. (psychiatryinvestigation.org)
- 1 By contrast, potential associations between chemokine and chemokine receptor polymorphisms and BD have been fundamen tally understudied and only MCP-1 gene polymorphisms have been investigated in patients with BD. (psychiatryinvestigation.org)
CCL23
- Another reported that IL-10, C-X-C motif chemokine ligand 10 (CXCL-10, formerly IFN-γ inducible protein 10) and CC chemokine ligand 2 (CCL2, formerly monocyte chemoattractant protein 1) levels were higher in patients with high viral loads ( 12 ), but patients with severe disease had higher levels of CXCL10 and CCL2 than did patients with less-severe cases. (cdc.gov)
- CCR receptors with specificity for CHEMOKINE CCL2 and several other CCL2-related chemokines. (lookformedical.com)
- Mature DC, which have been shown to react also to CCL2 and CCL20 [27], accumulate in muscle mass from IIM sufferers. (colinsbraincancer.com)
Receptors12
- A CC-type chemokine with specificity for CCR10 RECEPTORS. (lookformedical.com)
- A CC-type chemokine that is found at high levels in the THYMUS and has specificity for CCR4 RECEPTORS. (lookformedical.com)
- Like the CHEMOKINES themselves, the receptors can be divided into at least three structural branches: CR, CCR, and CXCR, according to variations in a shared cysteine motif. (lookformedical.com)
- A CC chemokine with specificity for CCR1 RECEPTORS and CCR5 RECEPTORS. (lookformedical.com)
- CCR receptors with specificity for CHEMOKINE CCL27. (lookformedical.com)
- CCR receptors with specificity for a broad variety of CC CHEMOKINES. (lookformedical.com)
- Chemokine CCL8 has specificity for CCR3 RECEPTORS and CCR5 RECEPTORS. (lookformedical.com)
- Chemokine receptors that are specific for CC CHEMOKINES. (lookformedical.com)
- A CC-type chemokine that is specific for CCR3 RECEPTORS. (lookformedical.com)
- CCR receptors with specificity for CHEMOKINE CCL19 and CHEMOKINE CCL21. (lookformedical.com)
- With the exception of CXCR4, which was expressed on 29% of endothelial cells, all other chemokine receptors (CXCR1, 2, 3, and CCR2) were expressed on less than 5% of the endothelial cell populations. (vu.nl)
- In previous studies, expression levels of several chemokine and chemokine receptors have been examined in patients with BD. (psychiatryinvestigation.org)
CCR610
- In silico analysis of SMAD4, CCL20, and CCR6 messenger RNA expression was performed on published transcriptomic data from human ulcerative colitis (UC), and colon and rectal cancer samples. (nih.gov)
- Immunohistochemistry for CCL20 and CCR6 was performed on human tissue microarrays comprising human UC-associated cancer specimens, Mice with conditional, epithelial-specific Smad4 loss with and without germline deletion of the Ccr6 gene were subjected to colitis and followed for up to 3 months. (nih.gov)
- A key downstream node in this regulation is suppression of epithelial CCL20 signaling to CCR6 in immune cells. (nih.gov)
- PPARδ dysregulation of CCL20/CCR6 axis promotes gastric adenocarcinoma carcinogenesis by remodeling gastric tumor microenvironment. (zhihuiya.com)
- Here, we examine the role of PPARδ-mediated Ccl20/Ccr6 signaling in GAC carcinogenesis and investigate the underlying mechanisms. (zhihuiya.com)
- RNAscope Duplex Assays were used to measure Ccl20 and Ccr6 levels in stomachs and spleens. (zhihuiya.com)
- PPARδ increased Ccl20 level to chemoattract Ccr6 + immunosuppressive cells, including tumor-associated macrophages, myeloid-derived suppressor cells and T regulatory cells, but decreased CD8 + T cells in gastric tissues. (zhihuiya.com)
- GSK3787 suppressed PPARδ-induced gastric immunosuppression by inhibiting Ccl20/Ccr6 axis. (zhihuiya.com)
- PPARδ dysregulation of Ccl20/Ccr6 axis promotes GAC carcinogenesis by remodeling gastric tumor microenvironment. (zhihuiya.com)
- MR120 (CCR6 antagonist 1b) is a potent, selective CCR6 antagonist, disrupts the CCL20-induced chemotaxis of CCR6+CD4+ T cells. (probechem.com)
Cytokines1
- Interferon pathway activation and cytokines/chemokines acting through CCR2 and CCR5 improved health results among children with severe CCHF. (cdc.gov)
Ligand2
- We previously reported that colon epithelial cell silencing of Smad4 increased epithelial expression of inflammatory genes, including the chemokine c-c motif chemokine ligand 20 (CCL20), and increased susceptibility to colitis-associated cancer. (nih.gov)
- Macrophage Inflammatory Protein-3 alpha (MIP-3a), also known as C-C Motif Chemokine Ligand 20 (CCL20) is a 70 amino acid chemokine (molecular weight 8.0 kDa). (quanterix.com)
CCL51
- Hippocampal neurons (2 DIV) control or treated with CXCL2, CCL5, CCL20, and CCL7 (1000 ng/ml) and immunostained for βIII-tubulin to reveal the axon morphology. (reprokine.com)
20202
- Lau S, Feitzinger A, Venkiteswaran G, Wang J, Lewellis SW, Koplinski CA, Peterson FC, Volkman BF, Meier-Schellersheim M, Knaut H. A negative-feedback loop maintains optimal chemokine concentrations for directional cell migration (2020) Nature Cell Biology 22 266-273. (xlockbio.com)
- Wedemeyer MJ, Mahn SA, Getschman AE, Peterson FC, Marchese A, McCorvy JD, and Volkman BF, The chemokine X-factor: structure-function analysis between CC and CXC chemokines at CXCR4 and ACKR3 (2020) J Biol Chem 295 13927-13939. (xlockbio.com)
CCL171
- In this study, we have characterized the T H 2-like chemokine profile (CCL17, CCL18, CCL20, CCL22) in patients with RRP and asked whether it was modulated in patients who had achieved significant clinical improvement. (biomedcentral.com)
Protein3
- Overall, CCL20 mRNA expression was not increased, but there was intense, selective CCL20 protein expression in the basal layer of the papillomas. (biomedcentral.com)
- Furthermore, Ccl20 protein levels increased in sera of Ppard TG mice starting at the age preceding gastric tumor development and further increased with GAC progression as the mice aged. (zhihuiya.com)
- Getschman AE, Imai Y, Larsen O, Peterson FC, Wu X, Rosenkilde MM, Hwang ST and Volkman BF, Protein engineering of the chemokine CCL20 prevents psoriasiform dermatitis in an IL-23-dependent murine model (2017) Proc Nat Acad Sci USA 114 12460-12465. (xlockbio.com)
Epithelial2
- In human UC-associated cancers, loss of epithelial SMAD4 was associated with increased CCL20 expression and CCR6+ cells. (nih.gov)
- In stomachs, PPARδ significantly increases chemokine Ccl20 expression in gastric epithelial cells while inducing gastric adenocarcinoma (GAC). (zhihuiya.com)
LYMPHOCYTES3
- A CC-type chemokine secreted by activated MONOCYTES and T-LYMPHOCYTES. (lookformedical.com)
- Group of chemokines with adjacent cysteines that are chemoattractants for lymphocytes, monocytes, eosinophils, basophils but not neutrophils. (lookformedical.com)
- A CXC chemokine that is chemotactic for T-LYMPHOCYTES and MONOCYTES. (lookformedical.com)
Cytokine1
- We examined cytokine/chemokine profiles of 9/12 case-patients compared with healthy controls at 3 time intervals. (cdc.gov)
Biomarker2
- Thus, the change in expression of these three plasma T H 2-like chemokines may, with future studies, prove to serve as a useful biomarker for predicting disease prognosis. (biomedcentral.com)
- CCL20 might be a potential biomarker for the early detection and progression of GAC. (zhihuiya.com)
Genes1
- This chemokine is encoded by multiple genes. (lookformedical.com)
Cells5
- Loss of SMAD4 in the colon epithelium increases CCL20 expression and chemoattraction of CCR6+ immune cells, contributing to greater susceptibility to colon cancer. (nih.gov)
- Additional chemokines attract mainly T-cells. (colinsbraincancer.com)
- The IFN-induced chemokines CXCL9C11 offer extremely selective lymphocyte recruitment bringing in subsets of Compact disc4+ and Compact 1235-82-1 IC50 disc8+ T-cells [24]. (colinsbraincancer.com)
- Increased degrees of CXCL12 are from the IIM, and the principal resources of the chemokine in the muscle mass are inflammatory cells and arteries. (colinsbraincancer.com)
- A significant and more general attractant for B-cells is normally CXCL13 or B-cell-attracting chemokine 1 [30], which is particularly prominent in the bigger perimysial infiltrates as well as the follicular buildings within DM muscles [31]. (colinsbraincancer.com)
Amino acid1
- Riutta SJ, Larsen O, Getschman AE, Rosenkilde MM, Hwang ST and Volkman BF, Mutational analysis of CCL20 reveals flexibility of N-terminal amino acid composition and length (2018) J Leuk Biol 104 423-434. (xlockbio.com)
Inflammatory1
- Cell surface glycoproteins that bind to chemokines and thus mediate the migration of pro-inflammatory molecules. (lookformedical.com)
Tissues1
- Among the results was evidence that there was differential chemokine mRNA expression by the papilloma tissues, which suggested that the virus might be able to polarize the patients' innate immune responses. (biomedcentral.com)
Expression1
- PGE 2 can bias the adaptive immune response away from an effective T H 1-like pattern ( 16 ), and can enhance expression of T H 2-like chemokines by innate immunocytes ( 16 , 17 ). (biomedcentral.com)
Levels1
- GSK3787 decreased the PPARδ-upregulated Ccl20 levels in sera of the mice. (zhihuiya.com)
Activation1
- A chemokine that is a chemoattractant for MONOCYTES and may also cause cellular activation of specific functions related to host defense. (lookformedical.com)
Mouse1
- A panel of 13 optimized proinflammatory chemokines in mouse sera were quantified by an enzyme-linked immunosorbent assay. (zhihuiya.com)
Ability1
- Despite their well-known involvement in neuroimmunologic processes, the pathogenic significance of chemokines, which are small signaling proteins with the ability to induce chemotaxis, has been relatively understudied in BD as compared with other immune system components. (psychiatryinvestigation.org)
CCL32
- CCL3 in Cancers Chemokine receptors are expressed on APCs and are promising targets for idiotype (Id) vaccines, the V antigenic determinants region produced by B lymphomas and multiple myelomas. (medscape.com)
- The most highly up-regulated genes in human skin feature those encoding cytokines (IL6 and IL24), chemokines (CCL3, CCL20, CXCL1, CXCL2, CXCL3 and CXCL5), the prostanoid synthesising enzyme COX-2 and members of the keratin gene family. (ox.ac.uk)
CXCL101
- The NF-κB pathway was the major signaling pathway affected by K13 expression, and genetic and pharmacological inhibitors of this pathway effectively blocked K13-induced transcriptional activation of the promoter of CXCL10, one of the chemokines whose expression was highly upregulated by K13. (biomedcentral.com)
CCL221
- [3] Its gene is located on human chromosome 16 along with some CC chemokines known as CCL17 and CCL22 . (wikidoc.org)
Ligands3
- Examples of such ligands include proinflammatory chemokines such as MIP3α/CCL20 or β-defensin mDF2β. (nih.gov)
- The aim of this study was to clarify the characteristics of the CXC chemokine superfamily induced by IFN-γ, namely CXCR3 ligands, in the airways of patients with asthma stratified by the differential proportion of granulocytes in sputum. (biomedcentral.com)
- Both ligands inhibited the release of chemokines mediated by IL-17A, with an IC50 of 20.9 ± 12.6 μM and 23.6 ± 11.8 μM for CCL20 and an IC50 of 26.7 ± 13.1 μM and 45.3 ± 13.0 μM for CXCL8. (ox.ac.uk)
Cytokines and chemokines3
- The primary function of IL-17A is certainly to coordinate regional tissue irritation via the upregulation of pro-inflammatory and neutrophil-mobilizing cytokines and chemokines [including IL-6 G-CSF TNF? (immune-source.com)
- Previous work has shown that the gene expression of cytokines and chemokines is positively correlated between species and that these factors can contribute to UVB-induced pain. (ox.ac.uk)
- Many of the top up-regulated genes were cytokines and chemokines, highlighting again their potential as pain mediators. (ox.ac.uk)
Dendritic cells1
- These strategies use proinflammatory chemokines to deliver antigens to immature dendritic cells (DCs) by targeting chemokine receptors differentially expressed on antigen presenting cells (APCs). (nih.gov)
CXCL53
- Modulation of expression of innate immunity markers CXCL5/ENA-78 and CCL20/MIP3alpha by protease-activated receptors (PARs) in human gingival epithelial cells. (nih.gov)
- Activation of PAR via proteolytic activity of thrombin and trypsin induces expression of CXCL5/ENA-78 and CCL20/MIP3alpha in a concentration-dependent manner. (nih.gov)
- The induction of CXCL5 and CCL20 via PAR2 was inhibited by PAR2 siRNA. (nih.gov)
Specificity1
- A knottin scaffold directs the CXC-chemokine-binding specificity of tick evasins. (peprotech.com)
Proinflammatory2
- IL8 is a proinflammatory chemokine. (aacc.org)
- Together, these results suggest that NiV C regulates expression of proinflammatory cytokines, therefore providing a signal responsible for the coordination of leukocyte recruitment and the chemokine-induced immune response and controlling the lethal outcome of the infection. (nartsignaling.com)
CCR21
- Interferon pathway activation and cytokines/chemokines acting through CCR2 and CCR5 improved health results among children with severe CCHF. (cdc.gov)
Adhesion1
- Soluble CX3CL1 potently chemoattracts T cells and monocytes , while the cell-bound chemokine promotes strong adhesion of leukocytes to activated endothelial cells, where it is primarily expressed. (wikidoc.org)
CXCL61
- CXCL6, also known as GCP-2 in humans, is a connective tissue-derived CXC chemokine that can signal through the CXCR1 and CXCR2 receptors. (peprotech.com)
Inflammation3
- Thus, modulation of EAE with C-C chemokine DNA vaccines is determined by targeting chemokines that are highly transcribed at the site of inflammation at the onset of disease. (medscape.com)
- Keratinocytes play an active role in initiating and maintenance of psoriatic skin inflammation by secreting chemokines and cytokines. (bvsalud.org)
- IL-17A produced by T cells potently upregulates the production of chemokine CCL20 in the keratinocytes, which further chemoattracts IL-17A-producing CCR6+ immune cells to the site of inflammation. (bvsalud.org)
Monocytes1
- CCL20 acts as a chemotactic factor that attracts lymphocytes and, slightly, neutrophils, but not monocytes (PubMed:9038201, PubMed:11352563). (nih.gov)
Humans1
- CX3CL1 is produced as a long protein (with 373-amino acid in humans) with an extended mucin -like stalk and a chemokine domain on top. (wikidoc.org)
Immune1
- In next part of the review, various chemokines with their specific role in altering immune response to combat various diseases especially cancers will be discussed. (medscape.com)
Human1
- Here we demonstrate that IL-23 and IL-1beta induced the development of human T(H)-17 cells expressing IL-17A, IL-17F, IL-22, IL-26, interferon-gamma, the chemokine CCL20 and transcription factor RORgammat. (nih.gov)
Abundance1
- There is no clear sequence similarity between beta-defensins and the chemokine MIP-3alpha, beyond an abundance of cationic residues and the presence of disulfide bonds. (nih.gov)
Activities1
- The discussed chemokines in this review, their synonyms, receptors, activities and sources were summarized in Table 4 . (medscape.com)
Role1
- This indicates a possible role for the chemokine in the protective plasticity process of synaptic scaling . (wikidoc.org)