BALB 3T3 Cells
Mice, Inbred Strains
Leishmania major
Species Specificity
Leishmaniasis, Cutaneous
Immunization
Disease Susceptibility
Interferon-gamma
Immunoglobulin G
Plasmacytoma
Interleukin-4
Cytokines
T-Lymphocytes
Th2 Cells
Lung
Th1 Cells
Immunoglobulin Idiotypes
Leishmaniasis
Mice, Nude
Hypersensitivity, Delayed
Antibody Formation
Immunity, Cellular
Neoplasm Transplantation
Immunization, Passive
Neoplasms, Experimental
Adjuvants, Immunologic
Antibody Specificity
CD4-Positive T-Lymphocytes
Injections, Intraperitoneal
Crosses, Genetic
Immunity, Innate
Lymphocyte Activation
Mice, Knockout
Leishmania tropica
Leukemia, Experimental
Enzyme-Linked Immunosorbent Assay
Mammary Tumor Virus, Mouse
B-Lymphocytes
Immunoglobulin E
Rodent Diseases
Mice, SCID
Macrophages
Sarcoma, Experimental
Lymph Nodes
Liver
Molecular Sequence Data
Immune Tolerance
Leishmania mexicana
Cross Reactions
Immunoglobulin Isotypes
Hybridomas
Vaccines, Synthetic
3T3 Cells
Transplantation, Isogeneic
Antibodies, Anti-Idiotypic
Antigens, Protozoan
Interleukin-12
Specific Pathogen-Free Organisms
RNA, Messenger
Virulence
Leishmaniasis, Visceral
Cell Division
Bacterial Vaccines
CD8-Positive T-Lymphocytes
Transplantation, Homologous
Amino Acid Sequence
Cytotoxicity, Immunologic
Corneal Transplantation
Allergens
Base Sequence
Lethal Dose 50
Leishmania donovani
Clone Cells
Bronchoalveolar Lavage Fluid
Interleukin-5
Eye Infections, Viral
Brucella abortus
Interleukin-10
Major Histocompatibility Complex
Brucellosis
Flow Cytometry
Antigens, Surface
Urethane
Dose-Response Relationship, Immunologic
Autoantibodies
Thymus Gland
Gammaretrovirus
Autoimmune Diseases
Respiratory Syncytial Virus Infections
Skin Transplantation
Macrophages, Peritoneal
Bronchial Hyperreactivity
Injections, Subcutaneous
Coxsackievirus Infections
T-Lymphocyte Subsets
Phenotype
Virus Replication
Immunogenetics
Antigens, Neoplasm
Immunity, Humoral
Skin
Adoptive Transfer
Haptens
Antibodies
Immunoglobulin M
Myocarditis
Binding Sites, Antibody
Mice, Transgenic
Killer Cells, Natural
Respiratory Syncytial Viruses
Filarioidea
Tumor Necrosis Factor-alpha
Isoantigens
Graft Rejection
Histocompatibility Antigens
Gene Expression Regulation
Immunoglobulin Allotypes
T-Lymphocytes, Regulatory
Genes
Cornea
Melioidosis
Sarcoma Viruses, Murine
Interleukin-2
Genetic Vectors
Lipopolysaccharides
Epitopes, T-Lymphocyte
DNA
Viral Vaccines
Immune Sera
Immunoglobulin Variable Region
Leishmania
Salmonella typhimurium
T-Lymphocytes, Helper-Inducer
Inflammation
Antibody Diversity
Dose-Response Relationship, Drug
Colony Count, Microbial
Muromegalovirus
Burkholderia pseudomallei
Anterior Chamber
Vaccines, Attenuated
Chromosome Mapping
Genetic Predisposition to Disease
Immunity
Gene Expression
Graft Survival
Models, Animal
Concanavalin A
Macrophage Activation
Cytotoxicity Tests, Immunologic
Reverse Transcriptase Polymerase Chain Reaction
Granuloma
Immunoglobulin Heavy Chains
Retroviridae
Injections, Intramuscular
Dendritic Cells
Respiratory Hypersensitivity
Leishmania infantum
Ear
Immunohistochemistry
Immunity, Active
Fungal Vaccines
Immunity, Mucosal
Overexpression of NP95 mRNA by tumor promoters in the promotion phase of a two-stage BALB/3T3 cell transformation assay. (1/136)
We studied altered gene expressions in BALB/3T3 cells treated by different tumor promoters in the promotion phase of a transformation assay, an in vitro model of a two-stage carcinogenicity test, using fluorescent mRNA differential display analysis. Expression of the NP95 gene, which was previously found to be the gene of a murine nuclear protein associated with cell proliferation, was increased in the cultures treated by 12-O-tetradecanoylphorbol-13-acetate (TPA), okadaic acid, and orthovanadate. The upregulation of NP95 mRNA was confirmed by reverse transcription-PCR, and Northern blot. TPA, okadaic acid, and orthovanadate enhanced cell proliferation as measured by a 5-bromo-2'-deoxyuridine incorporation assay. The expression level of NP95 mRNA was not affected by the treatment with typical carcinogens benzo[a]pyrene and 3-methylcholanthrene at concentrations at which they act as initiators of cell transformation. These facts may imply that the enhancement of cell transformation by these tumor promoters is due, at least in part, to the acceleration of cell proliferation. NP95 mRNA was also increased in the transformed BALB/3T3 cells. Overexpression of NP95 may also participate in the maintenance of the transformed phenotype. (+info)Beta-catenin inversely regulates vascular endothelial growth factor-D mRNA stability. (2/136)
The angiogenic and lymphangiogenic vascular endothelial growth factor (VEGF)-D is the only member of the VEGF family that is not induced by hypoxia or by serum factors, but its induction is mediated by direct cell-cell contact. Here we show that VEGF-D mRNA is down-modulated either by beta-catenin mobilization from the cell membrane, by activation of the Wnt signaling pathway, or by transfection with the beta-catenin stable mutant. Down-modulation of beta-catenin by means of RNA interference showed an increase of VEGF-D mRNA steady state in fibroblasts. The beta-catenin-dependent decrease of VEGF-D mRNA is indirect and mainly due to reduced VEGF-D mRNA stability, as demonstrated by experiments of mRNA decay in the presence of transcription or translation inhibitors. By transient transfection of chimeric constructs carrying fusion of VEGF-D sequences under the control of the cytomegalovirus early promoter, we demonstrated that beta-catenin negative regulation is on the VEGF-D mRNA 3'-untranslated region. We mapped the VEGF-D mRNA-destabilizing element to a sequence, conserved between mouse and human VEGF-D, which contains an AU-rich element of group I. These results unveiled a new regulatory pathway for VEGF-D, which explains, at least in part, VEGF-D regulation in tumor progression. (+info)Importance of amino acids of the central portion of the second intracellular loop of the gastrin-releasing Peptide receptor for phospholipase C activation, internalization, and chronic down-regulation. (3/136)
Little is known about the function of the central portion of the second intracellular loop (i2 loop) of peptide receptors in activation of downstream pathways and receptor modulatory processes such as receptor internalization or chronic down-regulation (DR). Recent data suggest a role for i2 loop hydrophobic amino acids in these processes. We used site-directed mutagenesis to address these issues with the gastrin-releasing peptide receptor (GRP-R). Each i2 loop residue from 142 to 148 was mutated and the receptors were expressed in Balb 3T3 cells. Two mutants showed a minimal (<2-fold) decrease in affinity. Five mutants showed decreased efficacy for activating phospholipase C (PLC). Two double mutants (IM143.147AA and VM144.147AA) showed a minimal decrease in affinity but had a decreased ability to fully activate PLC. Only the IM double mutation had decreased maximal internalization, whereas the R145A single mutant showed an increase, suggesting a tonic inhibitory role for Arg-145 in internalization. Three single and both double mutants showed decreases in receptor DR. There was a weak correlation between the extent of GRP-R internalization and the maximal PLC activation, whereas changes in the maximal PLC activation were significantly (p = 0.008) coupled to receptor DR. This study shows that amino acids of the i2 loop of the GRP-R are important in activation of PLC, internalization and down-regulation, but not for affinity. Our results support the proposal that internalization and chronic down-regulation have differing dependence on PLC and are largely independent processes, because some mutants showed no changes in internalization, but significant alterations in down-regulation. (+info)Synergistic regulation of the acute phase protein SIP24/24p3 by glucocorticoid and pro-inflammatory cytokines. (4/136)
SIP24/24p3 is a secreted murine acute phase protein which has been speculated to play an anti-inflammatory role in vivo. Recently SIP24/24p3 has been found to be able to specifically induce apoptosis in leukocytes. By using (35)S metabolic labeling method, we studied the regulation of SIP24/24p3 by glucocorticoid and pro-inflammatory cytokines IL-6 and TNF-alpha in cultured Balb/c 3T3 and BNL cells. The following results were observed: (1) dexamethasone induced the expression of SIP24/24p3 in both Balb/c 3T3 and BNL cells, the induction was more significant in BNL cells; (2) dexamethasone and IL-6 synergistically induced the expression of SIP24/24p3 in both Balb/c 3T3 and BNL cells; (3) in Balb/c 3T3 cells dexamethasone and TNF-alpha acted synergistically to induce the expression of SIP24/24p3, whereas in BNL cells dexamethasone and TNF-alpha induced the expression of SIP24/24p3 in an additive manner; (4) dexamethasone and IL-6/TNF-alpha acted synergistically in Balb/c 3T3 cells and additively in BNL cells to induce the expression of SIP24/24p3. The inducibility of SIP24/24p3 by multiple factors will help to explain its highly specific expression in vivo. The difference in the expression patterns of SIP24/24p3 in different cell types is also suggestive to its expression and regulation in hepatic and extrahepatic tissues. Finally, the fact that SIP24/24p3 protein can be induced by both pro-inflammatory as well as anti-inflammatory factors is indicative of the important role of SIP24/24p3 in the entire acute phase response process. (+info)Influence of type I collagen surface density on fibroblast spreading, motility, and contractility. (5/136)
We examine the relationships of three variables (projected area, migration speed, and traction force) at various type I collagen surface densities in a population of fibroblasts. We observe that cell area is initially an increasing function of ligand density, but that above a certain transition level, increases in surface collagen cause cell area to decline. The threshold collagen density that separates these two qualitatively different regimes, approximately 160 molecules/ microm(2), is approximately equal to the cell surface density of integrin molecules. These results suggest a model in which collagen density induces a qualitative transition in the fundamental way that fibroblasts interact with the substrate. At low density, the availability of collagen binding sites is limiting and the cells simply try to flatten as much as possible by pulling on the few available sites as hard as they can. The force per bond under these conditions approaches 100 pN, approximately equal to the force required for rupture of integrin-peptide bonds. In contrast, at high collagen density adhesion, traction force and motility are limited by the availability of free integrins on the cell surface since so many of these receptors are bound to the surface ligand and the force per bond is very low. (+info)Efficient replication of full-length murine leukemia viruses modified at the dimer initiation site regions. (6/136)
Retroviruses encapsidate two copies of full-length viral RNA molecules linked together as a dimeric genome. RNA stem loop structures harboring palindromic (or "kissing") loop sequences constitute important cis-elements for viral dimerization known as dimer initiation sites (DIS). In murine leukemia virus (MLV), a 10-mer and a 16-mer palindrome (DIS-1 and DIS-2, respectively) located in the viral leader region mediate dimerization in vitro and affect dimer stability of vector RNA in vivo. We have investigated the effect on viral replication of introducing deletions or nucleotide substitutions within these palindromes in a full-length MLV genome. Our results demonstrate that viruses modified at the dimer initiation site regions are viable and show wild-type levels of RNA encapsidation. One mutant lacking the DIS-1 palindrome was severely impaired and displayed an increased cellular ratio of spliced versus genomic RNA that most likely contributes to the inefficient replication. The implications for development of DIS-modified retrovirus-based vectors are discussed. (+info)AG490 inhibits G1-S traverse in BALB/c-3T3 cells following either mitogenic stimulation or exogenous expression of E2F-1. (7/136)
AG490, a member of the tryphostin family of protein kinase inhibitors, repressed G(0)-G(1) traverse in BALB/c-3T3 cells. While the early induction of STAT activity was repressed by AG490, extracellular signal-regulated kinase (ERK) activation was unaffected and a pattern of gene expression suggested that cells exited G(0) in the presence of the inhibitor. Although AG490 did not alter the induction of cyclin D1 protein, neither cyclin D1- nor cyclin D3-associated kinase activity was observed in growth-inhibited cells. Surprisingly, p130 was partially phosphorylated, and E2F3A protein was expressed in mitogen-stimulated AG490-treated cells despite the lack of cyclin D-associated kinase activity. These data suggest that AG490 inhibits a cellular pathway required for mid-G(0)-G(1) traverse that is located after the induction of early processes potentially mediated by E2F (although independent of cyclin D-associated kinase activity) but before the late G(1) increase in E2F-dependent transcription. Infection of AG490-treated cells with an E2F-1 adenovirus caused the induction of cyclin A, but could not overcome the drug-induced cell cycle arrest that was coincident with the repression of cyclin-dependent kinase 2 (cdk2)-associated kinase activation. We conclude that cdk2-associated kinase activity is modulated by a cellular process repressed by AG490. Furthermore, this cdk2-associated kinase activity is required for G(0)-G(1) traverse in some role other than the regulation of E2F-dependent transcription. (+info)Antisense thymidylate synthase electrogene transfer to increase uptake of radiolabeled iododeoxyuridine in a murine model. (8/136)
In vitro and in vivo experiments from our laboratory and others have suggested that the combination of thymidylate synthase (TS) inhibitor and radiolabeled iododeoxyuridine (IdUrd) is synergistic. Efficacy is limited by drug resistance, which is often mediated by TS overexpression. We designed an in vivo electrogene transfer (EGT) model for delivering antisense TS plasmid (ATS) into tumor to increase the subsequent efficacy of (131)I-IdUrd therapy. METHODS: Plasmid complementary to nucleotide 531-710 in the coding region of the mouse TS (mTS) mRNA was constructed. TS activity and (131)I-IdUrd DNA incorporation were determined 48 h after in vitro EGT of ATS to CT26 cells. In vivo therapeutic effect and radioactivity retained in tumor after various combinations of EGT ATS, 5-fluorouracil (5-FU), and continuous infusion of (131)I-IdUrd by osmotic minipump were determined. RESULTS: A reduction of TS activity was achieved after in vitro EGT ATS. Flow cytometry analysis indicated that ATS-treated cells were arrested at S phase. In the in vivo tumor model, the combination of EGT ATS and 5-FU was able to partially overcome 5-FU drug resistance. Sixty percent of tumors can be eradicated by the combination of EGT ATS, 5-FU, and infusion of (131)I-IdUrd. The tumors treated by EGT ATS had higher radioactivity retained 1 wk after (131)I-IdUrd therapy than after EGT of control plasmid. CONCLUSION: In situ EGT ATS can downregulate TS and increase the therapeutic effect of radiolabeled IdUrd therapy. The combination of EGT ATS, 5-FU, and (131)I-IdUrd may result in tumor eradication. (+info)A parasitic disease caused by a protozoan of the genus Leishmania, which is transmitted to humans by the bite of an infected sandfly. The most common form of the disease is characterized by skin lesions, which may be painful and disfiguring.
Other forms of leishmaniasis include:
1. Visceral leishmaniasis (kala-azar): A severe and potentially fatal form of the disease that affects several internal organs, including the spleen, liver, and bone marrow.
2. Mucocutaneous leishmaniasis: A form of the disease characterized by skin lesions and mucosal involvement, such as nose ulcers and mouth sores.
3. Diffuse cutaneous leishmaniasis: A form of the disease characterized by widespread skin involvement, often with a diffuse, papular rash.
4. Recidivans leishmaniasis: A form of the disease characterized by repeated episodes of skin lesions, often triggered by exposure to sandflies.
Symptoms of cutaneous leishmaniasis may include:
* Skin lesions, which may be painful and disfiguring
* Swelling of the affected limb
* Fever
* Fatigue
* Weight loss
Diagnosis is made by identifying the parasite in a skin scraping or biopsy specimen. Treatment typically involves antiparasitic medications, such as pentavalent antimonials or amphotericin B.
Preventive measures include avoiding sandfly bites, wearing protective clothing and insect repellents, and using screens on windows and doors to prevent sandflies from entering homes.
There are several types of disease susceptibility, including:
1. Genetic predisposition: This refers to the inherent tendency of an individual to develop a particular disease due to their genetic makeup. For example, some families may have a higher risk of developing certain diseases such as cancer or heart disease due to inherited genetic mutations.
2. Environmental susceptibility: This refers to the increased risk of developing a disease due to exposure to environmental factors such as pollutants, toxins, or infectious agents. For example, someone who lives in an area with high levels of air pollution may be more susceptible to developing respiratory problems.
3. Lifestyle susceptibility: This refers to the increased risk of developing a disease due to unhealthy lifestyle choices such as smoking, lack of exercise, or poor diet. For example, someone who smokes and is overweight may be more susceptible to developing heart disease or lung cancer.
4. Immune system susceptibility: This refers to the increased risk of developing a disease due to an impaired immune system. For example, people with autoimmune disorders such as HIV/AIDS or rheumatoid arthritis may be more susceptible to opportunistic infections.
Understanding disease susceptibility can help healthcare providers identify individuals who are at risk of developing certain diseases and provide preventive measures or early intervention to reduce the risk of disease progression. Additionally, genetic testing can help identify individuals with a high risk of developing certain diseases, allowing for earlier diagnosis and treatment.
In summary, disease susceptibility refers to the predisposition of an individual to develop a particular disease or condition due to various factors such as genetics, environment, lifestyle choices, and immune system function. Understanding disease susceptibility can help healthcare providers identify individuals at risk and provide appropriate preventive measures or early intervention to reduce the risk of disease progression.
Plasmacytoma is a type of plasma cell dyscrasia, which is a group of diseases that affect the production and function of plasma cells. Plasma cells are a type of white blood cell that produces antibodies to fight infections. In plasmacytoma, the abnormal plasma cells grow and multiply out of control, leading to a tumor.
There are several subtypes of plasmacytoma, including:
* solitary plasmacytoma: A single tumor that occurs in one location.
* multiple myeloma: A type of cancer that affects the bones and is characterized by an overgrowth of malignant plasma cells in the bone marrow.
* extramedullary plasmacytoma: A tumor that occurs outside of the bone marrow, such as in soft tissue or organs.
Plasmacytoma is usually diagnosed through a combination of physical examination, imaging tests such as X-rays or CT scans, and biopsy. Treatment typically involves chemotherapy and/or radiation therapy to destroy the abnormal cells. In some cases, surgery may be necessary to remove the tumor.
Plasmacytoma is a relatively rare cancer, but it can be aggressive and potentially life-threatening if left untreated. It is important for patients with symptoms of plasmacytoma to seek medical attention as soon as possible to receive an accurate diagnosis and appropriate treatment.
There are several different forms of leishmaniasis, including:
* Cutaneous leishmaniasis: This form of the disease causes skin sores, which can be painful and disfiguring.
* Visceral leishmaniasis: Also known as kala-azar, this form of the disease affects the internal organs and can be fatal if left untreated.
* Mucocutaneous leishmaniasis: This form of the disease causes sores on the skin and mucous membranes.
*Diffuse cutaneous leishmaniasis: This form of the disease causes widespread skin lesions.
Leishmaniasis can be diagnosed through a variety of methods, including:
* Physical examination and medical history: A doctor may look for signs of the disease, such as skin sores or swelling, and ask about the patient's travel history and exposure to sandflies.
* Laboratory tests: Blood and skin samples can be tested for the presence of the parasite using techniques such as microscopy, PCR, and serology.
* Imaging studies: X-rays, CT scans, and MRI scans can be used to visualize the spread of the disease in the body.
Treatment for leishmaniasis typically involves antiparasitic drugs, such as pentavalent antimonials, miltefosine, and amphotericin B. The specific treatment regimen will depend on the severity and location of the disease, as well as the patient's age, health status, and other factors. In some cases, surgery may be necessary to remove affected tissue.
Prevention measures for leishmaniasis include:
* Avoiding sandfly bites: Using insecticides, wearing protective clothing, and staying in well-screened areas can help prevent sandfly bites.
* Eliminating sandfly breeding sites: Removing debris and vegetation, and using insecticides to kill sandflies and their eggs can help reduce the risk of infection.
* Vaccination: There is currently no effective vaccine against leishmaniasis, but research is ongoing to develop one.
* Public education: Raising awareness about the disease and how it is transmitted can help prevent infections and reduce the burden on healthcare systems.
Overall, early diagnosis and treatment are key to preventing complications and improving outcomes for patients with leishmaniasis. In addition, public health measures such as insecticide use and vaccination may help reduce the incidence of the disease.
Examples of delayed hypersensitivity reactions include contact dermatitis (a skin reaction to an allergic substance), tuberculin reactivity (a reaction to the bacteria that cause tuberculosis), and sarcoidosis (a condition characterized by inflammation in various organs, including the lungs and lymph nodes).
Delayed hypersensitivity reactions are important in the diagnosis and management of allergic disorders and other immune-related conditions. They can be detected through a variety of tests, including skin prick testing, patch testing, and blood tests. Treatment for delayed hypersensitivity reactions depends on the underlying cause and may involve medications such as antihistamines, corticosteroids, or immunosuppressants.
Types of experimental neoplasms include:
* Xenografts: tumors that are transplanted into animals from another species, often humans.
* Transgenic tumors: tumors that are created by introducing cancer-causing genes into an animal's genome.
* Chemically-induced tumors: tumors that are caused by exposure to certain chemicals or drugs.
The use of experimental neoplasms in research has led to significant advances in our understanding of cancer biology and the development of new treatments for the disease. However, the use of animals in cancer research is a controversial topic and alternatives to animal models are being developed and implemented.
Examples of experimental leukemias include:
1. X-linked agammaglobulinemia (XLA): A rare inherited disorder that leads to a lack of antibody production and an increased risk of infections.
2. Diamond-Blackfan anemia (DBA): A rare inherited disorder characterized by a failure of red blood cells to mature in the bone marrow.
3. Fanconi anemia: A rare inherited disorder that leads to a defect in DNA repair and an increased risk of cancer, particularly leukemia.
4. Ataxia-telangiectasia (AT): A rare inherited disorder characterized by progressive loss of coordination, balance, and speech, as well as an increased risk of cancer, particularly lymphoma.
5. Down syndrome: A genetic disorder caused by an extra copy of chromosome 21, which increases the risk of developing leukemia, particularly acute myeloid leukemia (AML).
These experimental leukemias are often used in research studies to better understand the biology of leukemia and to develop new treatments.
1. Hantavirus pulmonary syndrome (HPS): This is a severe respiratory disease caused by the hantavirus, which is found in the urine and saliva of infected rodents. Symptoms of HPS can include fever, headache, muscle pain, and difficulty breathing.
2. Leptospirosis: This is a bacterial infection caused by the bacterium Leptospira, which is found in the urine of infected rodents. Symptoms can include fever, headache, muscle pain, and jaundice (yellowing of the skin and eyes).
3. Rat-bite fever: This is a bacterial infection caused by the bacterium Streptobacillus moniliformis, which is found in the saliva of infected rodents. Symptoms can include fever, headache, muscle pain, and swollen lymph nodes.
4. Lymphocytic choriomeningitis (LCM): This is a viral infection caused by the lymphocytic choriomeningitis virus (LCMV), which is found in the urine and saliva of infected rodents. Symptoms can include fever, headache, muscle pain, and meningitis (inflammation of the membranes surrounding the brain and spinal cord).
5. Tularemia: This is a bacterial infection caused by the bacterium Francisella tularensis, which is found in the urine and saliva of infected rodents. Symptoms can include fever, headache, muscle pain, and swollen lymph nodes.
These are just a few examples of the many diseases that can be transmitted to humans through contact with rodents. It is important to take precautions when handling or removing rodents, as they can pose a serious health risk. If you suspect that you have been exposed to a rodent-borne disease, it is important to seek medical attention as soon as possible.
Example sentence: The patient was diagnosed with experimental sarcoma and underwent a novel chemotherapy regimen that included a targeted therapy drug.
The symptoms of visceral leishmaniasis can vary depending on the severity of the infection, but may include:
* Fever
* Fatigue
* Loss of appetite
* Weight loss
* Enlargement of the liver and spleen
* Pain in the abdomen
* Anemia
* Low blood platelet count
* Low white blood cell count
If left untreated, visceral leishmaniasis can be fatal. Treatment is typically with antiparasitic drugs, such as miltefosine or amphotericin B, and supportive care to manage symptoms and prevent complications.
It is important to note that visceral leishmaniasis is a serious and potentially life-threatening condition, and prompt medical attention is necessary for effective treatment and management.
Some common types of viral eye infections include:
1. Conjunctivitis caused by adenovirus: This is a highly contagious form of conjunctivitis that often affects children and can be spread through close contact with an infected person or by touching contaminated surfaces.
2. Conjunctivitis caused by enterovirus: This type of conjunctivitis is also highly contagious and can be spread through contact with an infected person's saliva, mucus, or feces.
3. Herpetic keratitis: This is a rare form of viral eye infection that is caused by the herpes simplex virus and can lead to serious complications if left untreated.
4. Epidemic keratoconjunctivitis: This is a highly contagious form of conjunctivitis that is caused by adenovirus and can affect both children and adults.
Viral eye infections are typically diagnosed through a comprehensive eye exam, which may include a visual acuity test, a dilated eye exam, and/or a viral culture. Treatment for viral eye infections usually involves antiviral medication, cold compresses, and good hygiene practices to prevent the spread of the infection.
Prevention:
To prevent the spread of viral eye infections, it is important to practice good hygiene habits such as washing your hands frequently, avoiding close contact with people who are infected, and not sharing personal items like towels or makeup. If you have a viral eye infection, it is also important to avoid touching your eyes and to cover your mouth and nose when coughing or sneezing.
Conclusion:
Viral eye infections can be highly contagious and cause uncomfortable symptoms such as redness, discharge, and blurred vision. It is important to seek medical attention if you experience any of these symptoms, as they can lead to serious complications if left untreated. Good hygiene practices and antiviral medication can help prevent and treat viral eye infections.
There are several types of brucellosis, including:
1. Brucella abortus: This type is primarily found in cattle and is the most common form of the disease in humans.
2. Brucella suis: This type is found in pigs and is less common in humans.
3. Brucella melitensis: This type is found in sheep, goats, and other animals, and is more virulent than B. abortus.
4. Brucella canis: This type is found in dogs and is rare in humans.
The symptoms of brucellosis can vary depending on the severity of the infection and the individual's overall health. Common symptoms include:
1. Fever
2. Headache
3. Joint pain
4. Muscle pain
5. Swelling of the lymph nodes and spleen
6. Fatigue
7. Loss of appetite
8. Weight loss
In severe cases, brucellosis can cause complications such as:
1. Endocarditis (infection of the heart valves)
2. Meningitis (inflammation of the lining around the brain and spinal cord)
3. Osteomyelitis (infection of the bone)
4. Testicular inflammation in men
5. Epididymitis (inflammation of the epididymis, a tube that carries sperm from the testicle to the penis)
6. Inflammation of the heart muscle and valves
7. Pneumonia
8. Inflammation of the liver and spleen
Brucellosis is diagnosed through a combination of physical examination, laboratory tests, and imaging studies. Treatment typically involves antibiotics, and early treatment can help prevent complications. Prevention measures include avoiding contact with infected animals and ensuring proper hygiene practices when handling livestock or wild game.
Examples of autoimmune diseases include:
1. Rheumatoid arthritis (RA): A condition where the immune system attacks the joints, leading to inflammation, pain, and joint damage.
2. Lupus: A condition where the immune system attacks various body parts, including the skin, joints, and organs.
3. Hashimoto's thyroiditis: A condition where the immune system attacks the thyroid gland, leading to hypothyroidism.
4. Multiple sclerosis (MS): A condition where the immune system attacks the protective covering of nerve fibers in the central nervous system, leading to communication problems between the brain and the rest of the body.
5. Type 1 diabetes: A condition where the immune system attacks the insulin-producing cells in the pancreas, leading to high blood sugar levels.
6. Guillain-Barré syndrome: A condition where the immune system attacks the nerves, leading to muscle weakness and paralysis.
7. Psoriasis: A condition where the immune system attacks the skin, leading to red, scaly patches.
8. Crohn's disease and ulcerative colitis: Conditions where the immune system attacks the digestive tract, leading to inflammation and damage to the gut.
9. Sjögren's syndrome: A condition where the immune system attacks the glands that produce tears and saliva, leading to dry eyes and mouth.
10. Vasculitis: A condition where the immune system attacks the blood vessels, leading to inflammation and damage to the blood vessels.
The symptoms of autoimmune diseases vary depending on the specific disease and the organs or tissues affected. Common symptoms include fatigue, fever, joint pain, skin rashes, and swollen lymph nodes. Treatment for autoimmune diseases typically involves medication to suppress the immune system and reduce inflammation, as well as lifestyle changes such as dietary changes and stress management techniques.
RSV infections can cause a range of symptoms, including:
* Runny nose
* Decreased appetite
* Coughing
* Sneezing
* Wheezing
* Apnea (pauses in breathing)
* Blue-tinged skin and lips (cyanosis)
* Fever
* Inflammation of the lower respiratory tract (bronchiolitis)
* Pneumonia
In severe cases, RSV infections can lead to hospitalization and may require oxygen therapy or mechanical ventilation. In rare cases, RSV infections can be life-threatening, particularly in premature babies and infants with underlying medical conditions.
There is no specific treatment for RSV infections, but antiviral medications may be prescribed in severe cases. Treatment focuses on relieving symptoms and managing the infection, such as providing hydration and nutrition, administering oxygen therapy, and monitoring vital signs.
Prevention measures for RSV infections include:
* Frequent handwashing, especially after contact with an infected person or their secretions
* Avoiding close contact with anyone who has RSV infection
* Keeping children home from school or daycare if they are showing symptoms of RSV infection
* Practicing good hygiene, such as avoiding sharing utensils or personal items with anyone who is infected
There is currently no vaccine available to protect against RSV infections, but researchers are working on developing one.
The diagnosis of BHR is based on a combination of clinical, physiological, and imaging tests. The most common method used to assess BHR is the methacholine or histamine challenge test, which involves inhaling progressively increasing concentrations of these substances to measure airway reactivity. Other tests include exercise testing, hyperventilation, and mannitol challenge.
BHR is characterized by an increased responsiveness of the airways to various stimuli, such as allergens, cold or exercise, leading to inflammation and bronchoconstriction. This can cause symptoms such as wheezing, coughing, shortness of breath, and chest tightness.
There are several risk factors for BHR, including:
* Allergies
* Respiratory infections
* Exposure to environmental pollutants
* Genetic predisposition
* Obesity
* Smoking
Treatment of BHR typically involves the use of bronchodilators, corticosteroids, and other medications to reduce inflammation and airway constriction. In severe cases, surgical procedures such as lung volume reduction or bronchial thermoplasty may be necessary. Environmental modifications, such as avoiding triggers and using HEPA filters, can also help manage symptoms.
In summary, bronchial hyperreactivity is a condition characterized by an exaggerated response of the airways to various stimuli, leading to increased smooth muscle contraction and narrowing of the bronchi. It is commonly seen in asthma and other respiratory diseases, and can cause symptoms such as wheezing, coughing, shortness of breath, and chest tightness. Treatment typically involves medications and environmental modifications to reduce inflammation and airway constriction.
Coxsackievirus infections are a group of viral diseases caused by enteroviruses, primarily Coxsackie A and B viruses. These infections can affect various parts of the body, including the gastrointestinal tract, skin, and nervous system.
Types of Coxsackievirus Infections:
1. Hand, Foot, and Mouth Disease (HFMD): This is a common viral illness that affects children under the age of 10, causing fever, mouth sores, and a rash with blisters on the hands and feet.
2. Herpangina: A severe form of HFMD characterized by small ulcers in the mouth and throat.
3. Aseptic Meningitis: An inflammation of the meninges (protective membranes) around the brain and spinal cord, often caused by Coxsackievirus B.
4. Myocarditis: Inflammation of the heart muscle caused by Coxsackievirus B.
5. Pericarditis: Inflammation of the membrane surrounding the heart (pericardium) caused by Coxsackievirus B.
6. Pleurodynia (also known as Coxsackievirus pleurisy): A sudden onset of chest pain, fever, and cough caused by Coxsackievirus A.
7. Meningoradiculitis: Inflammation of the meninges and spinal nerves caused by Coxsackievirus B.
Symptoms of Coxsackievirus Infections:
The symptoms of coxsackievirus infections can vary depending on the type of infection and the individual affected. Common symptoms include:
* Fever
* Headache
* Muscle pain
* Sore throat
* Mouth sores (in HFMD)
* Rash (in HFMD)
* Blisters (in HFMD)
* Seizures (in severe cases)
* Meningitis (inflammation of the membranes surrounding the brain and spinal cord)
* Encephalitis (inflammation of the brain)
* Myocarditis (inflammation of the heart muscle)
* Pericarditis (inflammation of the membrane surrounding the heart)
* Pleurodynia (chest pain, fever, and cough)
* Meningoradiculitis (inflammation of the meninges and spinal nerves)
Diagnosis of Coxsackievirus Infections:
The diagnosis of coxsackievirus infections is based on a combination of clinical features, laboratory tests, and imaging studies. Laboratory tests may include:
* Blood tests to detect the presence of antibodies against the virus
* PCR (polymerase chain reaction) to detect the genetic material of the virus in respiratory or gastrointestinal secretions
* Culture of the virus from respiratory or gastrointestinal secretions
* Imaging studies such as X-rays, CT scans, MRI scans to evaluate the extent of inflammation or damage to organs.
Treatment and Management of Coxsackievirus Infections:
There is no specific treatment for coxsackievirus infections, but supportive care may be provided to manage symptoms and prevent complications. Supportive care may include:
* Rest and hydration
* Pain management with over-the-counter pain medications or prescription medications
* Antihistamines to reduce fever and relieve itching
* Antiviral medications in severe cases
* Oxygen therapy if necessary
* Intravenous fluids if dehydration is present.
Prevention of Coxsackievirus Infections:
Prevention of coxsackievirus infections is important, especially for high-risk individuals such as children and people with weakened immune systems. Prevention measures include:
* Practicing good hygiene, such as washing hands frequently, especially after using the bathroom or before eating
* Avoiding close contact with people who are sick
* Avoiding sharing food, drinks, or personal items with people who are sick
* Keeping children home from school or daycare if they are experiencing symptoms of a coxsackievirus infection
* Practicing safe sex to prevent the spread of the virus through sexual contact.
Complications of Coxsackievirus Infections:
Coxsackievirus infections can lead to complications, especially in high-risk individuals. Complications may include:
* Meningitis or encephalitis, which can be life-threatening
* Myocarditis, which can lead to heart failure
* Pericarditis, which can cause chest pain and difficulty breathing
* Retinitis, which can cause blindness
* Gastrointestinal bleeding
* Kidney damage or failure.
Prognosis for Coxsackievirus Infections:
The prognosis for coxsackievirus infections is generally good for most people, especially those with mild symptoms. However, high-risk individuals, such as children and people with weakened immune systems, may experience more severe illness and have a poorer prognosis.
Prevention of Coxsackievirus Infections:
Prevention is key to avoiding coxsackievirus infections. Some ways to prevent the spread of the virus include:
* Practicing good hygiene, such as washing your hands frequently and avoiding sharing personal items with people who are sick
* Avoiding close contact with people who are sick
* Keeping children home from school or daycare if they are experiencing symptoms of a coxsackievirus infection
* Practicing safe sex to prevent the spread of the virus through sexual contact.
Treatment of Coxsackievirus Infections:
There is no specific treatment for coxsackievirus infections, but symptoms can be managed with over-the-counter medications and home remedies. Some ways to manage symptoms include:
* Taking over-the-counter pain relievers, such as acetaminophen or ibuprofen, to reduce fever and relieve headache and body aches
* Drinking plenty of fluids to stay hydrated
* Resting and avoiding strenuous activities until symptoms improve
* Using a humidifier to relieve dryness and discomfort in the throat and nose.
Complications of Coxsackievirus Infections:
Coxsackievirus infections can lead to complications, such as:
* Meningitis: an inflammation of the protective membranes that cover the brain and spinal cord
* Encephalitis: an inflammation of the brain
* Myocarditis: an inflammation of the heart muscle
* Pericarditis: an inflammation of the membrane surrounding the heart
* Pleurodynia: a painful inflammation of the lining of the chest cavity.
It's important to seek medical attention if you or your child experiences any of these complications, as they can be serious and potentially life-threatening.
Conclusion:
Coxsackievirus infections are common and can cause a range of symptoms, from mild to severe. Prevention is key, and taking steps such as washing your hands frequently, avoiding close contact with people who are sick, and keeping children home from school or daycare when they are ill can help reduce the risk of transmission. If you suspect that you or your child has a coxsackievirus infection, it's important to seek medical attention if symptoms worsen or if complications develop. With prompt and appropriate treatment, most people with coxsackievirus infections recover fully.
The symptoms of myocarditis can vary depending on the severity of the inflammation and the location of the affected areas of the heart muscle. Common symptoms include chest pain, shortness of breath, fatigue, and swelling in the legs and feet.
Myocarditis can be difficult to diagnose, as its symptoms are similar to those of other conditions such as coronary artery disease or heart failure. Diagnosis is typically made through a combination of physical examination, medical history, and results of diagnostic tests such as electrocardiogram (ECG), echocardiogram, and blood tests.
Treatment of myocarditis depends on the underlying cause and severity of the condition. Mild cases may require only rest and over-the-counter pain medication, while more severe cases may require hospitalization and intravenous medications to manage inflammation and cardiac function. In some cases, surgery may be necessary to repair or replace damaged heart tissue.
Prevention of myocarditis is important, as it can lead to serious complications such as heart failure and arrhythmias if left untreated. Prevention strategies include avoiding exposure to viruses and other infections, managing underlying medical conditions such as diabetes and high blood pressure, and getting regular check-ups with a healthcare provider to monitor cardiac function.
In summary, myocarditis is an inflammatory condition that affects the heart muscle, causing symptoms such as chest pain, shortness of breath, and fatigue. Diagnosis can be challenging, but treatment options range from rest and medication to hospitalization and surgery. Prevention is key to avoiding serious complications and maintaining good cardiac health.
Melioidosis is typically acquired through contact with contaminated soil or water in tropical and subtropical regions of Asia and Africa. The bacteria can enter the body through open wounds, cuts, or through the eyes, nose, or mouth. Once inside the body, the bacteria can multiply and cause a wide range of symptoms including fever, chills, headache, muscle and joint pain, and skin lesions.
If left untreated, melioidosis can lead to serious complications such as sepsis, meningitis, and pneumonia, which can be fatal. The disease is diagnosed through a combination of physical examination, laboratory tests, and imaging studies. Treatment typically involves antibiotics, and early treatment is essential for effective management of the disease.
In addition to being an important medical condition, melioidosis is also of interest to researchers studying the bacteria that cause the disease. Burkholderia pseudomallei has been found to have a unique ability to survive in a variety of environments, including soil and water, and has been studied for its potential as a bioterrorism agent.
In summary, melioidosis is a serious bacterial infection caused by Burkholderia pseudomallei that can affect multiple organ systems and cause severe illness if left untreated. It is typically acquired through contact with contaminated soil or water in tropical and subtropical regions of Asia and Africa and is diagnosed through a combination of physical examination, laboratory tests, and imaging studies. Early treatment is essential for effective management of the disease.
In animals, hepatitis can be caused by a variety of agents, including:
1. Viral hepatitis: Caused by viruses such as feline infectious peritonitis (FIP) in cats and canine infectious hepatitis (CIH) in dogs.
2. Bacterial hepatitis: Caused by bacteria such as Leptospira spp., which can be transmitted through contact with contaminated water or soil.
3. Parasitic hepatitis: Caused by parasites such as liver flukes (Fasciola spp.) and tapeworms (Taenia spp.).
4. Toxic hepatitis: Caused by exposure to certain drugs, chemicals, or environmental toxins.
5. Genetic hepatitis: Caused by inherited genetic disorders such as hemophilia in dogs and cats.
The clinical signs of animal hepatitis can vary depending on the cause and severity of the disease, but may include lethargy, loss of appetite, vomiting, diarrhea, abdominal pain, and jaundice (yellowing of the skin and eyes). Diagnosis is based on a combination of physical examination, laboratory tests (such as blood tests and liver biopsy), and imaging studies.
Treatment of animal hepatitis depends on the underlying cause and may include supportive care, antibiotics, anti-inflammatory medications, and in some cases, surgery or liver transplantation. In severe cases, animal hepatitis can be fatal if left untreated, so early diagnosis and aggressive treatment are essential for a successful outcome.
There are several key features of inflammation:
1. Increased blood flow: Blood vessels in the affected area dilate, allowing more blood to flow into the tissue and bringing with it immune cells, nutrients, and other signaling molecules.
2. Leukocyte migration: White blood cells, such as neutrophils and monocytes, migrate towards the site of inflammation in response to chemical signals.
3. Release of mediators: Inflammatory mediators, such as cytokines and chemokines, are released by immune cells and other cells in the affected tissue. These molecules help to coordinate the immune response and attract more immune cells to the site of inflammation.
4. Activation of immune cells: Immune cells, such as macrophages and T cells, become activated and start to phagocytose (engulf) pathogens or damaged tissue.
5. Increased heat production: Inflammation can cause an increase in metabolic activity in the affected tissue, leading to increased heat production.
6. Redness and swelling: Increased blood flow and leakiness of blood vessels can cause redness and swelling in the affected area.
7. Pain: Inflammation can cause pain through the activation of nociceptors (pain-sensing neurons) and the release of pro-inflammatory mediators.
Inflammation can be acute or chronic. Acute inflammation is a short-term response to injury or infection, which helps to resolve the issue quickly. Chronic inflammation is a long-term response that can cause ongoing damage and diseases such as arthritis, asthma, and cancer.
There are several types of inflammation, including:
1. Acute inflammation: A short-term response to injury or infection.
2. Chronic inflammation: A long-term response that can cause ongoing damage and diseases.
3. Autoimmune inflammation: An inappropriate immune response against the body's own tissues.
4. Allergic inflammation: An immune response to a harmless substance, such as pollen or dust mites.
5. Parasitic inflammation: An immune response to parasites, such as worms or fungi.
6. Bacterial inflammation: An immune response to bacteria.
7. Viral inflammation: An immune response to viruses.
8. Fungal inflammation: An immune response to fungi.
There are several ways to reduce inflammation, including:
1. Medications such as nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, and disease-modifying anti-rheumatic drugs (DMARDs).
2. Lifestyle changes, such as a healthy diet, regular exercise, stress management, and getting enough sleep.
3. Alternative therapies, such as acupuncture, herbal supplements, and mind-body practices.
4. Addressing underlying conditions, such as hormonal imbalances, gut health issues, and chronic infections.
5. Using anti-inflammatory compounds found in certain foods, such as omega-3 fatty acids, turmeric, and ginger.
It's important to note that chronic inflammation can lead to a range of health problems, including:
1. Arthritis
2. Diabetes
3. Heart disease
4. Cancer
5. Alzheimer's disease
6. Parkinson's disease
7. Autoimmune disorders, such as lupus and rheumatoid arthritis.
Therefore, it's important to manage inflammation effectively to prevent these complications and improve overall health and well-being.
Also known as: Corneal inflammation, Eye inflammation, Keratoconjunctivitis, Ocular inflammation.
The term "Salmonella Infections, Animal" is used to distinguish these infections from Salmonella infections that are caused by contaminated food or water, which are referred to as "Salmonella Infections, Human."
Explanation: Genetic predisposition to disease is influenced by multiple factors, including the presence of inherited genetic mutations or variations, environmental factors, and lifestyle choices. The likelihood of developing a particular disease can be increased by inherited genetic mutations that affect the functioning of specific genes or biological pathways. For example, inherited mutations in the BRCA1 and BRCA2 genes increase the risk of developing breast and ovarian cancer.
The expression of genetic predisposition to disease can vary widely, and not all individuals with a genetic predisposition will develop the disease. Additionally, many factors can influence the likelihood of developing a particular disease, such as environmental exposures, lifestyle choices, and other health conditions.
Inheritance patterns: Genetic predisposition to disease can be inherited in an autosomal dominant, autosomal recessive, or multifactorial pattern, depending on the specific disease and the genetic mutations involved. Autosomal dominant inheritance means that a single copy of the mutated gene is enough to cause the disease, while autosomal recessive inheritance requires two copies of the mutated gene. Multifactorial inheritance involves multiple genes and environmental factors contributing to the development of the disease.
Examples of diseases with a known genetic predisposition:
1. Huntington's disease: An autosomal dominant disorder caused by an expansion of a CAG repeat in the Huntingtin gene, leading to progressive neurodegeneration and cognitive decline.
2. Cystic fibrosis: An autosomal recessive disorder caused by mutations in the CFTR gene, leading to respiratory and digestive problems.
3. BRCA1/2-related breast and ovarian cancer: An inherited increased risk of developing breast and ovarian cancer due to mutations in the BRCA1 or BRCA2 genes.
4. Sickle cell anemia: An autosomal recessive disorder caused by a point mutation in the HBB gene, leading to defective hemoglobin production and red blood cell sickling.
5. Type 1 diabetes: An autoimmune disease caused by a combination of genetic and environmental factors, including multiple genes in the HLA complex.
Understanding the genetic basis of disease can help with early detection, prevention, and treatment. For example, genetic testing can identify individuals who are at risk for certain diseases, allowing for earlier intervention and preventive measures. Additionally, understanding the genetic basis of a disease can inform the development of targeted therapies and personalized medicine."
Granulomas are formed in response to the presence of a foreign substance or an infection, and they serve as a protective barrier to prevent the spread of the infection and to isolate the offending agent. The granuloma is characterized by a central area of necrosis, surrounded by a ring of immune cells, including macrophages and T-lymphocytes.
Granulomas are commonly seen in a variety of inflammatory conditions, such as tuberculosis, leprosy, and sarcoidosis. They can also occur as a result of infections, such as bacterial or fungal infections, and in the context of autoimmune disorders, such as rheumatoid arthritis.
In summary, granuloma is a term used to describe a type of inflammatory lesion that is formed in response to the presence of a foreign substance or an infection, and serves as a protective barrier to prevent the spread of the infection and to isolate the offending agent.
Respiratory hypersensitivity can be diagnosed through medical history, physical examination, and allergy testing. Treatment options include avoidance of allergens, medication, such as antihistamines or corticosteroids, and immunotherapy, which involves exposing the person to small amounts of the allergen over time to build up their tolerance.
Some people with respiratory hypersensitivity may experience more severe symptoms, such as asthma, which can be life-threatening if left untreated. It is important for individuals with respiratory hypersensitivity to work closely with their healthcare provider to manage their condition and prevent complications.
Orthomyxoviridae infections are a group of viral infections caused by the Orthomyxoviridae family of viruses, which includes influenza A and B viruses, as well as other related viruses. These infections can affect both humans and animals and can cause a range of symptoms, from mild to severe.
The most common type of Orthomyxoviridae infection is seasonal influenza, which occurs when the virus is transmitted from person to person through the air or by contact with infected surfaces. Other types of Orthomyxoviridae infections include:
1. Pandemic influenza: This occurs when a new strain of the virus emerges and spreads quickly around the world, causing widespread illness and death. Examples of pandemic influenza include the Spanish flu of 1918 and the Asian flu of 1957.
2. Avian influenza: This occurs when birds are infected with the virus and can be transmitted to humans through close contact with infected birds or their droppings.
3. Swine influenza: This occurs when pigs are infected with the virus and can be transmitted to humans through close contact with infected pigs or their droppings.
4. H5N1 and H7N9: These are two specific types of bird flu viruses that have caused serious outbreaks in humans in recent years.
Symptoms of Orthomyxoviridae infections can include fever, cough, sore throat, runny nose, muscle aches, and fatigue. In severe cases, these infections can lead to pneumonia, bronchitis, and other respiratory complications, as well as hospitalization and even death.
Diagnosis of Orthomyxoviridae infections is typically made through a combination of physical examination, medical history, and laboratory tests, such as PCR (polymerase chain reaction) or viral culture. Treatment is generally focused on relieving symptoms and supporting the immune system, with antiviral medications may be used in severe cases.
Prevention of Orthomyxoviridae infections can include avoiding close contact with infected birds or pigs, wearing protective clothing and gear when handling animals, and practicing good hygiene such as washing hands frequently. Vaccines are also available for some species of birds and pigs to protect against these viruses.
Overall, Orthomyxoviridae is a family of viruses that can cause serious illness in humans and other animals, and it's important to take precautions to prevent exposure and spread of these viruses.
1. Activation of oncogenes: Some viruses contain genes that code for proteins that can activate existing oncogenes in the host cell, leading to uncontrolled cell growth.
2. Inactivation of tumor suppressor genes: Other viruses may contain genes that inhibit the expression of tumor suppressor genes, allowing cells to grow and divide uncontrollably.
3. Insertional mutagenesis: Some viruses can insert their own DNA into the host cell's genome, leading to disruptions in normal cellular function and potentially causing cancer.
4. Epigenetic changes: Viral infection can also cause epigenetic changes, such as DNA methylation or histone modification, that can lead to the silencing of tumor suppressor genes and the activation of oncogenes.
Viral cell transformation is a key factor in the development of many types of cancer, including cervical cancer caused by human papillomavirus (HPV), and liver cancer caused by hepatitis B virus (HBV). In addition, some viruses are specifically known to cause cancer, such as Kaposi's sarcoma-associated herpesvirus (KSHV) and Merkel cell polyomavirus (MCV).
Early detection and treatment of viral infections can help prevent the development of cancer. Vaccines are also available for some viruses that are known to cause cancer, such as HPV and hepatitis B. Additionally, antiviral therapy can be used to treat existing infections and may help reduce the risk of cancer development.
Body weight is an important health indicator, as it can affect an individual's risk for certain medical conditions, such as obesity, diabetes, and cardiovascular disease. Maintaining a healthy body weight is essential for overall health and well-being, and there are many ways to do so, including a balanced diet, regular exercise, and other lifestyle changes.
There are several ways to measure body weight, including:
1. Scale: This is the most common method of measuring body weight, and it involves standing on a scale that displays the individual's weight in kg or lb.
2. Body fat calipers: These are used to measure body fat percentage by pinching the skin at specific points on the body.
3. Skinfold measurements: This method involves measuring the thickness of the skin folds at specific points on the body to estimate body fat percentage.
4. Bioelectrical impedance analysis (BIA): This is a non-invasive method that uses electrical impulses to measure body fat percentage.
5. Dual-energy X-ray absorptiometry (DXA): This is a more accurate method of measuring body composition, including bone density and body fat percentage.
It's important to note that body weight can fluctuate throughout the day due to factors such as water retention, so it's best to measure body weight at the same time each day for the most accurate results. Additionally, it's important to use a reliable scale or measuring tool to ensure accurate measurements.
There are several types of lymphoma, including:
1. Hodgkin lymphoma: This is a type of lymphoma that originates in the white blood cells called Reed-Sternberg cells. It is characterized by the presence of giant cells with multiple nucleoli.
2. Non-Hodgkin lymphoma (NHL): This is a type of lymphoma that does not meet the criteria for Hodgkin lymphoma. There are many subtypes of NHL, each with its own unique characteristics and behaviors.
3. Cutaneous lymphoma: This type of lymphoma affects the skin and can take several forms, including cutaneous B-cell lymphoma and cutaneous T-cell lymphoma.
4. Primary central nervous system (CNS) lymphoma: This is a rare type of lymphoma that develops in the brain or spinal cord.
5. Post-transplantation lymphoproliferative disorder (PTLD): This is a type of lymphoma that develops in people who have undergone an organ transplant, often as a result of immunosuppressive therapy.
The symptoms of lymphoma can vary depending on the type and location of the cancer. Some common symptoms include:
* Swollen lymph nodes
* Fever
* Fatigue
* Weight loss
* Night sweats
* Itching
Lymphoma is diagnosed through a combination of physical examination, imaging tests (such as CT scans or PET scans), and biopsies. Treatment options for lymphoma depend on the type and stage of the cancer, and may include chemotherapy, radiation therapy, immunotherapy, or stem cell transplantation.
Overall, lymphoma is a complex and diverse group of cancers that can affect people of all ages and backgrounds. While it can be challenging to diagnose and treat, advances in medical technology and research have improved the outlook for many patients with lymphoma.
A type of keratitis caused by the herpes simplex virus (HSV). It is characterized by the presence of small, discrete ulcers on the surface of the cornea, along with inflammation and edema. The lesions are usually self-limiting but can be painful and may lead to scarring or perforation of the cornea if left untreated.
Synonyms: herpetic keratitis, HSV keratitis
See also: bacterial keratitis, fungal keratitis, avulsive keratitis, neurotrophic keratitis
Source: Medical Dictionary for Regulatory Activities (MedDRA)
Note: This term is used in the medical field to describe a specific type of inflammation of the cornea caused by the herpes simplex virus. It is important to note that this term is not a diagnosis, but rather a descriptor of the cause of the inflammation. A proper diagnosis can only be made by a qualified medical professional through a comprehensive examination and appropriate testing.
There are several types of hypersensitivity reactions, including:
1. Type I hypersensitivity: This is also known as immediate hypersensitivity and occurs within minutes to hours after exposure to the allergen. It is characterized by the release of histamine and other chemical mediators from immune cells, leading to symptoms such as hives, itching, swelling, and difficulty breathing. Examples of Type I hypersensitivity reactions include allergies to pollen, dust mites, or certain foods.
2. Type II hypersensitivity: This is also known as cytotoxic hypersensitivity and occurs within days to weeks after exposure to the allergen. It is characterized by the immune system producing antibodies against specific proteins on the surface of cells, leading to their destruction. Examples of Type II hypersensitivity reactions include blood transfusion reactions and serum sickness.
3. Type III hypersensitivity: This is also known as immune complex hypersensitivity and occurs when antigens bind to immune complexes, leading to the formation of deposits in tissues. Examples of Type III hypersensitivity reactions include rheumatoid arthritis and systemic lupus erythematosus.
4. Type IV hypersensitivity: This is also known as delayed-type hypersensitivity and occurs within weeks to months after exposure to the allergen. It is characterized by the activation of T cells, leading to inflammation and tissue damage. Examples of Type IV hypersensitivity reactions include contact dermatitis and toxic epidermal necrolysis.
The diagnosis of hypersensitivity often involves a combination of medical history, physical examination, laboratory tests, and elimination diets or challenges. Treatment depends on the specific type of hypersensitivity reaction and may include avoidance of the allergen, medications such as antihistamines or corticosteroids, and immunomodulatory therapy.
Herpes simplex virus 1 (HSV-1) typically causes cold sores or fever blisters that appear on the lips, mouth, or nose. While herpes simplex virus 2 (HSV-2) is responsible for genital herpes which affects the genital area, buttocks, and anal area.
The infection can be spread through direct contact with an infected person's saliva, mucus, or skin, even if there are no visible sores present. Symptoms of herpes simplex may include itching, burning, tingling, redness, and small blisters that burst and ooze fluid.
There is no cure for herpes simplex, but medications can help manage symptoms and shorten the duration of an outbreak. Antiviral drugs such as acyclovir, famciclovir, and valacyclovir are commonly used to treat herpes simplex.
A viral infection that affects the liver and is transmitted to animals through contact with infected feces, urine, or saliva. The condition can be caused by several different viruses, including hepatitis A, B, C, D, and E. Symptoms of animal hepatitis may include loss of appetite, vomiting, diarrhea, lethargy, fever, and jaundice (yellowing of the skin and eyes). In severe cases, the infection can cause liver failure and death.
Prevention:
* Avoid contact with infected animals
* Practice good hygiene, such as washing hands frequently
* Keep pets up to date on vaccinations and preventatives
* Avoid drinking water or eating food that may be contaminated with feces or urine from infected animals
* Use protective clothing and equipment when handling animals that may be infected
Treatment:
* Supportive care, such as fluids and electrolytes to prevent dehydration and maintain blood pressure
* Antiviral medications in severe cases
* Hospitalization for severe cases or those that do not respond to treatment
Prognosis:
* Depends on the severity of the infection and the underlying health status of the animal. In general, the prognosis is good for animals that receive prompt and appropriate treatment.
Complications:
* Liver failure
* Sepsis (blood infection)
* Kidney failure
* Death
Prevalence:
* Widespread in animals, especially in those that are kept in close quarters or have poor living conditions.
Affected Organ:
* Liver
CNV can cause vision loss and blindness if left untreated. It can also increase the risk of complications such as cataracts, glaucoma, and corneal ulcers.
There are several treatment options for CNV, including:
1. Anti-vascular endothelial growth factor (VEGF) injections: These medications can help reduce the growth of new blood vessels and preserve vision.
2. Photodynamic therapy: This involves the use of a light-sensitive medication and low-intensity laser to damage and shrink the new blood vessels.
3. Corneal transplantation: In severe cases, a corneal transplant may be necessary to replace the damaged or diseased cornea with a healthy one.
4. Surgical removal of the neovascularized tissue: This can be done through a surgical procedure called vitrectomy, where the new blood vessels are removed and the eye is filled with a gas or oil bubble.
Early detection and treatment of CNV are crucial to prevent vision loss and improve outcomes. Ophthalmologists use a range of diagnostic tests such as imaging studies and visual acuity assessments to diagnose and monitor the progression of the condition.
There are several triggers that can cause sneezing, including:
1. Allergens: Allergic reactions to pollen, dust mites, mold and other substances can cause sneezing.
2. Cold and flu viruses: These viruses can cause inflammation in the nasal passages and sinuses, leading to sneezing.
3. Sinus infections: Bacterial or fungal infections of the sinuses can cause sneezing.
4. Irritants: Exposure to irritants such as smoke, dust, and strong odors can cause sneezing.
5. Hormonal changes: Changes in hormone levels during pregnancy or menstruation can lead to increased nasal secretions and sneezing.
Sneezing can be treated with over-the-counter medications such as antihistamines, decongestants, and saline nasal sprays. If the sneezing is persistent or accompanied by other symptoms such as a fever, facial pain or swelling, it is important to see a healthcare professional for proper diagnosis and treatment.
In some cases, sneezing can be a sign of a more serious condition such as a sinus infection, meningitis or encephalitis. If you experience any of the following symptoms along with sneezing, seek medical attention immediately:
1. Severe headache
2. Fever over 101°F (38.3°C)
3. Facial pain or swelling
4. Difficulty breathing or swallowing
5. Nasal discharge that is thick and yellow or greenish in color
6. Seizures or convulsions
7. Change in mental status or confusion
In summary, sneezing during pregnancy can be caused by a variety of factors, including hormonal changes, allergies, and respiratory infections. If you experience persistent or severe sneezing during pregnancy, it is important to see a healthcare professional for proper diagnosis and treatment. Additionally, if you experience any other symptoms along with sneezing, seek medical attention immediately as these could be signs of a more serious condition.
Mast cell sarcoma is most commonly seen in the skin, but it can also arise in other parts of the body such as the spleen, liver, or gastrointestinal tract. The tumors are usually large, irregularly shaped masses that can be firm or soft to the touch. They may ulcerate and bleed easily, leading to swelling and discomfort.
The symptoms of mast cell sarcoma can vary depending on the location and size of the tumor. They may include:
* A lump or mass that may be painless or tender to the touch
* Swelling in the affected area
* Abdominal pain
* Diarrhea or constipation
* Fatigue
* Fevers
* Night sweats
Mast cell sarcoma is rare and accounts for only about 1-2% of all skin tumors. It is more common in dogs than cats and tends to affect older animals. The exact cause of mast cell sarcoma is not known, but genetic factors and environmental triggers may play a role.
Treatment options for mast cell sarcoma depend on the location and stage of the tumor. Surgery is often the first line of treatment to remove the tumor and any affected tissue. Additional therapies such as radiation, chemotherapy, or immunotherapy may be recommended based on the severity of the disease and the patient's overall health.
Prognosis for mast cell sarcoma varies depending on several factors, including the size and location of the tumor, the effectiveness of treatment, and the patient's overall health. In general, the prognosis is guarded and early detection and treatment are important to improve outcomes. With prompt and appropriate therapy, some patients with mast cell sarcoma can achieve long-term remission or even cure. However, in advanced cases or those that are resistant to treatment, the prognosis may be poorer.
The exact cause of fibrosarcoma is not known, but it is believed to be linked to genetic mutations that occur during a person's lifetime. Some risk factors for developing fibrosarcoma include previous radiation exposure, chronic inflammation, and certain inherited conditions such as neurofibromatosis type 1 (NF1).
The symptoms of fibrosarcoma can vary depending on the location and size of the tumor. In some cases, there may be no symptoms until the tumor has grown to a significant size. Common symptoms include pain, swelling, and limited mobility in the affected limb. If the tumor is near a nerve, it can also cause numbness or tingling sensations in the affected area.
Diagnosis of fibrosarcoma typically involves a combination of imaging tests such as X-rays, CT scans, and MRI scans, as well as a biopsy to confirm the presence of cancer cells. Treatment options for fibrosarcoma may include surgery, radiation therapy, and chemotherapy, depending on the size and location of the tumor, as well as the patient's overall health.
Prognosis for fibrosarcoma is generally good if the tumor is caught early and treated aggressively. However, if the cancer has spread to other parts of the body (metastasized), the prognosis is generally poorer. In some cases, the cancer can recur after treatment, so it is important for patients to follow their doctor's recommendations for regular check-ups and follow-up testing.
Overall, fibrosarcoma is a rare and aggressive form of cancer that can be challenging to diagnose and treat. However, with early detection and appropriate treatment, many people with this condition can achieve long-term survival and a good quality of life.
1. Conjunctivitis: This is an infection of the conjunctiva, which is the thin membrane that covers the white part of the eye and the inside of the eyelids. It is often caused by Streptococcus pneumoniae or Haemophilus influenzae bacteria.
2. Corneal ulcers: These are open sores that develop on the surface of the cornea, which is the clear dome-shaped surface at the front of the eye. Corneal ulcers can be caused by a variety of bacteria, including Staphylococcus aureus and Streptococcus pyogenes.
3. Endophthalmitis: This is an infection that occurs inside the eye, often as a complication of cataract surgery or other types of ocular surgery. It can be caused by a variety of bacteria, including Staphylococcus aureus and Streptococcus epidermidis.
4. Keratitis: This is an infection of the cornea that can be caused by a variety of bacteria, including Pseudomonas aeruginosa and Acinetobacter baumannii.
5. Retinitis: This is an infection of the retina, which is the layer of tissue at the back of the eye that senses light and sends visual signals to the brain. Retinitis can be caused by a variety of bacteria, including Haemophilus influenzae and Streptococcus pneumoniae.
Bacterial eye infections can cause a range of symptoms, including redness, swelling, discharge, pain, and blurred vision. Treatment typically involves antibiotic eye drops or ointments, and in more severe cases, oral antibiotics may be prescribed. It is important to seek medical attention if you experience any symptoms of a bacterial eye infection, as early treatment can help prevent complications and improve outcomes.
The diagnosis of pulmonary eosinophilia is based on a combination of clinical symptoms, physical examination findings, and laboratory tests such as chest X-rays, blood tests, and bronchoalveolar lavage (BAL) fluid analysis.
Treatment of pulmonary eosinophilia depends on the underlying cause and may include medications such as corticosteroids, antihistamines, or antibiotics, as well as lifestyle modifications such as avoiding allergens and managing stress. In severe cases, hospitalization may be necessary to monitor and treat the condition.
Some common symptoms of pulmonary eosinophilia include:
* Coughing
* Shortness of breath (dyspnea)
* Chest tightness or discomfort
* Fatigue
* Wheezing
* Recurrent respiratory infections
Complications of pulmonary eosinophilia can include:
* Respiratory failure
* Asthma exacerbation
* Chronic obstructive pulmonary disease (COPD)
* Pneumonia or other respiratory infections
* Airway obstruction
It is important to seek medical attention if you experience any of these symptoms, as early diagnosis and treatment can help prevent complications and improve outcomes.
Dermatitis, contact can be acute or chronic, depending on the severity and duration of the exposure. In acute cases, the symptoms may resolve within a few days after removing the offending substance. Chronic dermatitis, on the other hand, can persist for weeks or even months, and may require ongoing treatment to manage the symptoms.
The symptoms of contact dermatitis can vary depending on the individual and the severity of the exposure. Common symptoms include:
* Redness and inflammation of the skin
* Itching and burning sensations
* Swelling and blistering
* Cracks or fissures in the skin
* Difficulty healing or recurring infections
In severe cases, contact dermatitis can lead to complications such as:
* Infection with bacteria or fungi
* Scarring and disfigurement
* Emotional distress and anxiety
Diagnosis of contact dermatitis is typically made based on the patient's medical history and physical examination. Allergic patch testing may also be performed to identify specific allergens that are causing the condition.
Treatment for contact dermatitis usually involves avoiding the offending substance and using topical or oral medications to manage symptoms. In severe cases, systemic corticosteroids or immunosuppressants may be prescribed. Phototherapy and alternative therapies such as herbal remedies or acupuncture may also be considered.
Prevention of contact dermatitis involves identifying and avoiding substances that cause an allergic reaction or skin irritation. Individuals with a history of contact dermatitis should take precautions when handling new substances, and should be aware of the potential for cross-reactivity between different allergens.
1,1,2,2-Tetrachloroethane
Warren Jackson Pledger
List of MeSH codes (A11)
3T3 cells
CSNK1D
Adipogenesis
CXCL1
Jonathan Stamler
Eosinophil cationic protein
Creator: Nathans, Daniel, 1928-1999 / Subject: BALB 3T3 Cells and Simian virus 40 / Exhibit Tags: enzymes - Daniel Nathans -...
ARCHIVED - Environment and Climate Change Canada - Screening Assessment for the Challenge Naphthalene
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Ecm gel | Sigma-Aldrich
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DailyMed - VENLAFAXINE HYDROCHLORIDE- venlafaxine tablet, extended release
MESH TREE NUMBER CHANGES - 2014 MeSH. July 29, 2013
Human/Mouse/Rat Chk1 Antibody AF1630: R&D Systems
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DeCS 2004 - Novos termos
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Assay6
- The NRU cytotoxicity assay procedure is a cell survival/viability chemosensitivity assay based on the ability of viable cells to incorporate and bind neutral red (NR), a supravital dye. (nih.gov)
- Such changes brought about by the action of xenobiotics result in a decreased uptake and binding of NR. It is thus possible to distinguish between viable, damaged, or dead cells, which is the basis of this assay. (nih.gov)
- DNAs from five CdCl(2)-induced transformed cell lines were isolated and gene transfection assay was performed using NIH-3T3 cells. (cdc.gov)
- Determined by a cell proliferation assay using Balb/c 3T3 cells. (peprotech.com)
- The ED50 as determined in a cell proliferation assay using Balb/3T3 mouse embryonic fibroblast cells is less than 3 ug/ml. (joplink.net)
- Using a radioactive estrone sulfate (E 1 S) conversion assay, we detected STS activity in cultured NIH-3T3 cells. (cotinis.com)
Fibroblast cell line1
- This study was designed to characterize STS activity in a mouse fibroblast cell line (NIH-3T3). (cotinis.com)
Embryonic1
- Patterns of plasminogen activator production in cultured normal embryonic cells. (rupress.org)
Vitro7
- The 3T3 NRU test will be performed to analyze the in vitro toxicity of 60 blinded/coded test chemicals. (nih.gov)
- Tetraarsenic oxide-induced inhibition of malignant glioma cell invasion in vitro via a decrease in matrix metalloproteinase secretion and protein kinase B phosphorylation. (sigmaaldrich.com)
- MURINE leukaemia viruses (MLV) cause tumours of haemopoietic origin in vivo 1,2 , but although they replicate in vitro , they generally do not transform cells. (nature.com)
- We now report that MLV-A can be defective for virus replication and show that this agent directly transforms 3T3 cells in vitro . (nature.com)
- Aim of study was to determine if 835.62 MHz FDMA or 847.74 MHz CDMA radiations have any genotoxic effects that induce neoplastic transformations on C3H 10T1/2 cells in vitro . (emf-portal.org)
- Perocco P, Paolini M, Mazzullo M, Biagi GL and Cantelli-Forti G. (1999) -Carotene as enhancer of cell transforming activity of powerful carcinogens and cigarette-smoke condensate on BALB/c 3T3 cells in vitro. (nih.gov)
- U-87 MG cells are used as in vitro models of human glioblastoma cells to investigate the cytotoxic effect of chemotherapeutic drugs towards cancer cells. (altogen.com)
Fibroblasts1
- Our results could have important implications regarding local estrogen production by STS in fibroblasts , which are the most common connective tissue cells in the body, and on possible regulation of local estrogen levels by cortisol. (cotinis.com)
Toxicology1
- The U-87 glioblastoma cell line is widely used in transfection studies to examine the toxicology of potential treatment drugs. (altogen.com)
Cytotoxicity1
- Cytotoxicity is expressed as a concentration dependent reduction of the uptake of the NR after chemical exposure thus providing a sensitive, integrated signal of both cell integrity and growth inhibition. (nih.gov)
Apoptosis6
- 12. BCR signals target p27(Kip1) and cyclin D2 via the PI3-K signalling pathway to mediate cell cycle arrest and apoptosis of WEHI 231 B cells. (nih.gov)
- Two CRC cell lines (Colo 320DM and SW480) were treated with MSP and assessed for viability by trypan blue exclusion, for cell cycle distribution by flow cytometry, for apoptosis by annexin V labeling, for mitochondria potential by rhodamine 123 staining and for changes in the levels of proteins involved in cell cycle control or apoptosis by immunoblotting. (scirp.org)
- Abu Bakar and colleagues revealed that the ethanol extract from the seed kernel of Mangifera pajang could inhibit the growth and induce G2/M arrest of cell cycle and apoptosis on MCF-7 and MDA-MB-231 cells [14] , indicating the potential role of Mango seed kernel extract on cancer treatment or prevention. (scirp.org)
- Here, we investigated the effect of the ethanol extract from the seed kernel of Mangifera indica (MSP) on the growth, cell cycle and apoptosis of two CRC cells and revealed the potential role of MSP on CRC chemoprevention and treatment. (scirp.org)
- These pathways included cell cycle controlling, cell signaling pathway, cell apoptosis and adhesion [10]. (a-inhibitor.com)
- Pim-1 is mainly involved in cell cycle progression, apoptosis and transcriptional activation. (pimsignaling.com)
Regulation2
- 16. A pivotal role of cyclin D3 and cyclin-dependent kinase inhibitor p27 in the regulation of IL-2-, IL-4-, or IL-10-mediated human B cell proliferation. (nih.gov)
- With regard to regulation, treatments of cultured NIH-3T3 cells revealed that cortisol and the synthetic glucocorticoids dexamethasone and prednisolone decreased STS activity, as we have found for cell lines from other tissues. (cotinis.com)
Malignant4
- 2. Antiproliferative function of p27kip1 is frequently inhibited in highly malignant Burkitt's lymphoma cells. (nih.gov)
- As a consequence result, transformed foci were the final outcome of transforming cells in a malignant state. (a-inhibitor.com)
- U87 is a human glioblastoma cell line that was established from a malignant brain tumor. (altogen.com)
- Glioblastoma is a highly malignant tumor that originates from astrocytes and can be extremely difficult to eradicate due to it comprising many different cell types. (altogen.com)
Mouse3
- Cell lines developed from disaggregated BALB/c mouse embryos. (nih.gov)
- An unbiased screen for CNS cells showing c-Fos activation during experimental autoimmune encephalomyelitis (EAE), a mouse model for multiple sclerosis (MS), was developed by using inducible, TetTag c-Fos reporter mice that label activated cells with a temporally stable, nuclear green fluorescent protein (GFP). (eneuro.org)
- In this study, the application of this system is reported for targeting Rag genes to produce mutant mouse NIH/3T3 cell line. (cotinis.com)
Protocol2
- Protocol for automated production of human stem cell derived liver spheres. (peprotech.com)
- DNA plasmid expressing GAPDH or siRNA targeting GAPDH were transfected into U87 cells following Altogen Biosystems transfection protocol. (altogen.com)
Promoted cell proliferation1
- Higher concentrations of FGF1 promoted cell proliferation upon short-term stimulation, whereas prolonged treatment induced the expression of osteogenic markers even with low concentrations. (springermedizin.de)
Mammalian cells2
- Healthy mammalian cells, when maintained in culture, continuously divide and multiply over time. (nih.gov)
- Studies have been performed to determine if cadmium chloride (CdCl(2)) can induce morphological cell transformation, DNA from CdCl(2)-induced transformed cells can transform other mammalian cells, and the transformed cells induced by CdCl(2) can form tumors in nude mice. (cdc.gov)
Genes4
- He used duplicate copies of bands for CRYBP1, for Type II collagen, for Type X collagen, and for GAPDH and 18S EtBr stained control bands to falsely represent results of RNA expression from these different genes in ATDC5 cells. (nih.gov)
- Finally, in ferrets given high dose beta-carotene supplements and exposed to smoke, there also were elevated expressions of C-jun and C-fos genes, which are involved in cell proliferation. (nih.gov)
- Cell number, percentage of Ki67-positive cells, and expression of osteoblast- and fibroblast-specific genes were examined. (springermedizin.de)
- To find out the genes associated with cancer biological pathways involved in transformation and tumorigenesis, we transformed normal IEC-6 cells to cancer cells by treatment with cancerogenic agent of MNNG and PMA. (a-inhibitor.com)
Mice4
- Non-transformed BALB/c-3T3 cells and cells from 10 transformed cell lines induced by CdCl(2) were injected into both axillary regions of nude mice. (cdc.gov)
- All 10 CdCl(2)-induced transformed cell lines formed fibrosarcomas in nude mice within 39 days of inoculation. (cdc.gov)
- Within this time period, no tumors were found in nude mice injected with non-transformed BALB/c-3T3 cells. (cdc.gov)
- In addition, this Abelson virus (MLV-A) in conjunction with MLV-M causes rapid appearance of immunoglobulin-producing plasmacytomas in BALB/c mice primed with oil 8 . (nature.com)
Line7
- 7. 1,25-Dihydroxyvitamin D3 induces differentiation of a retinoic acid-resistant acute promyelocytic leukemia cell line (UF-1) associated with expression of p21(WAF1/CIP1) and p27(KIP1). (nih.gov)
- Western blot shows lysates of NRK rat normal kidney cell line, U2OS human osteosarcoma cell line, MCF-7 human breast cancer cell line, CEM human T-lymphoblastoid cell line, and Balb/3T3 mouse embryonic fibroblast cell line. (rndsystems.com)
- IEC-6 cell line was derived from normal rat intestinal epithelia [20]. (a-inhibitor.com)
- Human cell line models may lead to breakthroughs in brain cancer research and innovative treatment approaches that are essential for glioblastoma patients. (altogen.com)
- U-87 MG is a human glioblastoma cell line derived from a stage three 44-year-old Caucasian female. (altogen.com)
- U-87 is a hypodiploid human cell line with the modal chromosome number of 44 that occurs in 48% of cells. (altogen.com)
- Altogen Biosystems provides optimized lipid-based transfection kits for this cell line. (altogen.com)
Induce2
- DNA from all five CdCl(2)-induced transformed cell lines tested was found to induce varying degrees of transfection-mediated transformation in NIH-3T3 cells. (cdc.gov)
- To determine if exposure to FDMA or CDMA has any epigenetic effects that can promote neoplastic transformation , cells were also first exposed to 4.5 Gy of X-rays to induce the transformation process and then exposed to the above irradiations ( SAR = 0.6 W/kg) for 42 days. (emf-portal.org)
Associated with cyclin2
Concentrations2
- BALB/c-3T3 cells were treated with different concentrations of CdCl(2) for 72 h. (cdc.gov)
- The influence of different concentrations of FGF1 (12.5-200 ng/mL) on growth and proliferation of HPdLF cells was analyzed over 20 days by counting cell numbers and the percentage of Ki67-positive cells. (springermedizin.de)
Western Blot1
- At 72 hours post-transfection the cells were analyzed by Western Blot for protein expression levels (normalized by total protein, 10 µg of total protein loaded per each well). (altogen.com)
Tumor6
- p27/KIP1-cyclin D3 colocalization in tumor cells. (nih.gov)
- However, the promoters, which do not damage DNA directly, can facilitate tumor development from initiated cells. (a-inhibitor.com)
- Now, more and more chemicals have CBL0137 manufacturer been identified as tumor promoters in experimental animals and in cell transformation models, and their molecular mechanisms have been undoubtedly elucidated [8]. (a-inhibitor.com)
- An important advantage of the targeted tumor treatment is lowering the cyto- and genotoxicity of active substance towards healthy cells. (springer.com)
- The challenge the nanomedicine is now facing is to find the most effective way of the tumor cells eradication [ 13 ]. (springer.com)
- Some of these cells react to treatment well, and others can be utterly unresponsive to drugs, as stated by the American Brain Tumor Association (ABTA). (altogen.com)
Viability2
- Their protective effects on skin cell viability, ROS production, mitochondrial membrane potential, liposomal permeability, and DNA integrity were investigated. (bvsalud.org)
- The cell viability in our sonication test cell was comparable to that of commercial culture plates with bottoms constructed with silicone membrane. (bvsalud.org)
Differentiation4
- Multilayered dense collagen-silk fibroin hybrid: a platform for mesenchymal stem cell differentiation towards chondrogenic and osteogenic lineages. (sigmaaldrich.com)
- 9. Key role of the cyclin-dependent kinase inhibitor p27kip1 for embryonal carcinoma cell survival and differentiation. (nih.gov)
- 10. Cell cycle exit during terminal erythroid differentiation is associated with accumulation of p27(Kip1) and inactivation of cdk2 kinase. (nih.gov)
- FGFs play multiple roles in biological functions, including angiogenesis, mitogenesis, cell differentiation and wound repair. (joplink.net)
Gene1
- We transformed IEC-6 cells, and identified the altered gene expression by rat Oligo GEArray microarray of the six biological pathways involved in transformation and tumorigenesis. (a-inhibitor.com)
Collagen2
- However, collagen gels exhibit unstable geometrical properties, arising from extensive cell-mediated contraction. (sigmaaldrich.com)
- He also used duplicate copies of bands to falsely represent the RNA expression in ATDC5 cells grown under different conditions for either collagen Type II in Figure 3, MCB 2000 or collagen [alpha]1(X) in Figure 5 in MCB 22:4256-4267, 2002. (nih.gov)
Glial2
- More than 95% of the GFP + cells showed glial fibrillary acidic protein (GFAP) immunoreactivity-in contrast to absent or rare labeling of neurons, microglia, and infiltrating immune cells-which constituted ieAstrocytes that linearly increased in number with progression of EAE. (eneuro.org)
- Glioblastoma is the most common and aggressive type of brain cancer, and it arises from the glial cells in the brain. (altogen.com)
Epithelial2
- Differences in the biological effects of crocidolite asbestos and two glass fibres on epithelial lung cells. (cdc.gov)
- 4. Transforming growth factor beta(1) selectively inhibits the cyclic AMP-dependent proliferation of primary thyroid epithelial cells by preventing the association of cyclin D3-cdk4 with nuclear p27(kip1). (nih.gov)
Connective1
- Breast cancer cells invading the connective tissues outside the mammary lobule or duct immerse in a reservoir of extracellular matrix (ECM) that is structurally and biochemically distinct from that of their site of origin. (sigmaaldrich.com)
Astrocytes4
- FGF-acidic is a non-glycosylated heparin binding growth factor that is expressed in the brain, kidney, retina, smooth muscle cells, bone matrix, osteoblasts, astrocytes and endothelial cells. (peprotech.com)
- Astrocytes have prominent roles in central nervous system (CNS) function and disease, with subpopulations defined primarily by morphologies and molecular markers often determined in cell culture. (eneuro.org)
- ieAstrocyte s thus represent a functionally defined subset of disease-linked astrocytes that are the first and predominant CNS cell population activated during EAE, and that track with disease severity in vivo . (eneuro.org)
- A new, functionally defined in vivo subpopulation of astrocytes termed immediate-early astrocytes ( ieAstrocyte s) was identified as the first and predominant CNS cell type showing c-Fos activation, in an animal model of multiple sclerosis (MS). ieAstrocyte s track with disease severity. (eneuro.org)
Proteins1
- Using Franz diffusion cell systems studied the transdermal effect of DSCH and then examined the percutaneous rate and molecular weight distribution of percutaneous proteins (PP). (cotinis.com)
Regulatory2
- Targeted delivery of regulatory macrophages to lymph nodes interferes with T cell priming by preventing the formation of stable immune synapses. (peprotech.com)
- This is consistent with the idea that cortisol inhibits STS in NIH-3T3 cells through a regulatory mechanism rather than by substrate inhibition. (cotinis.com)
Osteogenic1
- AscA promotes cell growth more markedly than FGF1 in short-term cultures, whereas FGF1 induced osteogenic cell fate more strongly in long-term culture. (springermedizin.de)
Morphological2
- These results indicate that CdCl(2) is capable of inducing morphological cell transformation and that the transformed cells induced by CdCl(2) are potentially tumorigenic. (cdc.gov)
- This was also confirmed by an atomic force microscopy study of morphological changes in HaCaT cells or a study conducted on a 3D skin model. (bvsalud.org)
19981
- 1998. Activation of alveolar macrophages and peripheral red blood cells in rats exposed to fibers/particles. (cdc.gov)
Survival1
- 11. Overall survival in aggressive B-cell lymphomas is dependent on the accumulation of alterations in p53, p16, and p27. (nih.gov)
Lung1
- 1994. Mesothelial cell proliferation: A nonspecific response to lung injury associated with fibrosis. (cdc.gov)
Lines1
- MSP induces cell cycle arrest and apoptotic death in two CRC cell lines. (scirp.org)
Results2
- RESULTS: The sonication test cells were 3D printed from polylactic acid material, which was not toxic to the cells. (bvsalud.org)
- Preliminary results have already revealed that the use of a -emitting radionuclides has significant therapeutic effects for the treatment of disseminated disease, permitting selective cell-by-cell targeted therapy. (nih.gov)
Inhibitor2
- 6. Expression of cyclin-dependent kinase inhibitor p27(Kip1) in AIDS-related diffuse large-cell lymphomas is associated with Epstein-Barr virus-encoded latent membrane protein 1. (nih.gov)
- Indeed, altered miRNAs expression has been reported in many types of cancer cells, although the Wnt inhibitor functional significance of these changes has yet to be fully addressed [13, 14]. (a-inhibitor.com)
Eradicate1
- We hope these parallel areas of research will be used in the clinic in the future to eradicate residual cancer cells while allowing physicians to monitor the progress of this therapy via targeted macromolecular MRI contrast agents. (nih.gov)
Potential1
- Transforming and carcinogenic potential of cadmium chloride in BALB/c-3T3 cells. (cdc.gov)
Alterations1
- Alterations of the cell surface or the sensitive lysosomal membrane lead to lysosomal fragility and other changes that gradually become irreversible. (nih.gov)
Human1
- However, the effect of its seed kernel extract (MSP) on the growth of human colorectal carcinoma cells (CRC) has not yet been evaluated. (scirp.org)
Dependent2
- Ciclopirox acts by chelation of polyvalent cations (Fe 3+ or Al 3+ ), resulting in the inhibition of the metal-dependent enzymes that are responsible for the degradation of peroxides within the fungal cell. (nih.gov)
- The elaboration of PA by normal cells is dependent upon their metabolic activity, such that the level of serum supplementation and the growth phase of the culture directly influence the level of cell-associated PA observed. (rupress.org)
Activity4
- 17. Cyclin D3-associated kinase activity is regulated by p27kip1 in BALB/c 3T3 cells. (nih.gov)
- We also found that microsomes prepared from NIH-3T3 cells had relatively high STS activity and that cytosols had low activity , consistent with the known distribution of this enzyme to the endoplasmic reticulum. (cotinis.com)
- The reduction in STS activity by dexamethasone in whole cells was rversed by the glucocorticoid receptor antagonist RU-486, indicating that glucocorticoid downregulation of STS activity is receptor mediated. (cotinis.com)
- the low-passage cells then lose this PA activity after reaching confluence, while the 3T3 cells retain it indefinitely. (rupress.org)
Membrane1
- Silicone membrane HT-6240, which was used to construct the bottom of the test cell, was found to reduce ultrasound energy minimally. (bvsalud.org)
Immune1
- however, in animal models such as experimental autoimmune encephalomyelitis (EAE), immune cells, particularly CD4 + T cells, infiltrate the CNS to initiate demyelination and neurodegeneration. (eneuro.org)
Methods1
- METHODS: Optimal dimensions of the test cell were determined through measurements conducted in a water sonication tank using 3D-printed test objects. (bvsalud.org)
Distinct1
- Distinct phenotypes of cancer cells on tissue matrix gel. (sigmaaldrich.com)
Diffusion1
- NR is a weak cationic dye that readily penetrates cell membranes by non-ionic diffusion and accumulates intracellularly in lysosomes. (nih.gov)
Cycle3
- MSP inhibited proliferation by blocking cell cycle progression at G1 (SW480) or S (Colo 320DM) phase and inducing apoptotic death. (scirp.org)
- The Chk1 checkpoint kinase is an integral member of a signaling cascade that controls cell cycle progression. (rndsystems.com)
- In turn, Chk1 phosphorylates downstream effectors, such as p53 or the Cdc25 phosphatases to halt cell cycle progression and allow time for repair of incurred damage. (rndsystems.com)
Investigate2
- A proteomic approach to investigate AuNPs effects in Balb/3T3 cells. (sigmaaldrich.com)
- Thus, it is becoming crucial to assess their safety and adequately investigate the complexity of cell-nanoparticles interactions. (sigmaaldrich.com)
Expression3
- 14. Expression of the retinoblastoma protein in low-grade B-cell lymphoma: relationship to cyclin D1. (nih.gov)
- Forty-eight hours post-transfection, the cells were harvested and analyzed by real-time PCR for GAPD mRNA expression levels. (altogen.com)
- Protein expression of GAPDH in U87 cells. (altogen.com)