Differentiated epithelial cells of the INTESTINAL MUCOSA, found in the basal part of the intestinal crypts of Lieberkuhn. Paneth cells secrete GROWTH FACTORS, digestive enzymes such as LYSOZYME and antimicrobial peptides such as cryptdins (ALPHA-DEFENSINS) into the crypt lumen.
DEFENSINS found in azurophilic granules of neutrophils and in the secretory granules of intestinal PANETH CELLS.
Chelating agent used for heavy metal poisoning and assay. It causes diabetes.
The portion of the GASTROINTESTINAL TRACT between the PYLORUS of the STOMACH and the ILEOCECAL VALVE of the LARGE INTESTINE. It is divisible into three portions: the DUODENUM, the JEJUNUM, and the ILEUM.
Family of antimicrobial peptides that have been identified in humans, animals, and plants. They are thought to play a role in host defenses against infections, inflammation, wound repair, and acquired immunity.
Lining of the INTESTINES, consisting of an inner EPITHELIUM, a middle LAMINA PROPRIA, and an outer MUSCULARIS MUCOSAE. In the SMALL INTESTINE, the mucosa is characterized by a series of folds and abundance of absorptive cells (ENTEROCYTES) with MICROVILLI.
A basic enzyme that is present in saliva, tears, egg white, and many animal fluids. It functions as an antibacterial agent. The enzyme catalyzes the hydrolysis of 1,4-beta-linkages between N-acetylmuramic acid and N-acetyl-D-glucosamine residues in peptidoglycan and between N-acetyl-D-glucosamine residues in chitodextrin. EC 3.2.1.17.
The smallest member of the MATRIX METALLOPROTEINASES. It plays a role in tumor progression.
The section of the alimentary canal from the STOMACH to the ANAL CANAL. It includes the LARGE INTESTINE and SMALL INTESTINE.
A glandular epithelial cell or a unicellular gland. Goblet cells secrete MUCUS. They are scattered in the epithelial linings of many organs, especially the SMALL INTESTINE and the RESPIRATORY TRACT.
Inflammation of any segment of the ILEUM and the ILEOCECAL VALVE.
The distal and narrowest portion of the SMALL INTESTINE, between the JEJUNUM and the ILEOCECAL VALVE of the LARGE INTESTINE.
A chronic transmural inflammation that may involve any part of the DIGESTIVE TRACT from MOUTH to ANUS, mostly found in the ILEUM, the CECUM, and the COLON. In Crohn disease, the inflammation, extending through the intestinal wall from the MUCOSA to the serosa, is characteristically asymmetric and segmental. Epithelioid GRANULOMAS may be seen in some patients.
Protein precursors, also known as proproteins or prohormones, are inactive forms of proteins that undergo post-translational modification, such as cleavage, to produce the active functional protein or peptide hormone.
Tumors or cancer of the INTESTINES.
Pathological processes in any segment of the INTESTINE from DUODENUM to RECTUM.
Cells found throughout the lining of the GASTROINTESTINAL TRACT that contain and secrete regulatory PEPTIDE HORMONES and/or BIOGENIC AMINES.
DEFENSINS found mainly in epithelial cells.
A segment of the LOWER GASTROINTESTINAL TRACT that includes the CECUM; the COLON; and the RECTUM.
A worm-like blind tube extension from the CECUM.
Condensed areas of cellular material that may be bounded by a membrane.
ENTEROCOLITIS with extensive ulceration (ULCER) and NECROSIS. It is observed primarily in LOW BIRTH WEIGHT INFANT.
The middle portion of the SMALL INTESTINE, between DUODENUM and ILEUM. It represents about 2/5 of the remaining portion of the small intestine below duodenum.
Inflammation involving the skin of the extremities, especially the hands and feet. Several forms are known, some idiopathic and some hereditary. The infantile form is called Gianotti-Crosti syndrome.
A NOD signaling adaptor protein that contains two C-terminal leucine-rich domains which recognize bacterial PEPTIDOGLYCAN. It signals via an N-terminal capase recruitment domain that interacts with other CARD SIGNALING ADAPTOR PROTEINS such as RIP SERINE-THEONINE KINASES. The protein plays a role in the host defense response by signaling the activation of CASPASES and the MAP KINASE SIGNALING SYSTEM. Mutations of the gene encoding the nucleotide oligomerization domain 2 protein have been associated with increased susceptibility to CROHN DISEASE.
The shortest and widest portion of the SMALL INTESTINE adjacent to the PYLORUS of the STOMACH. It is named for having the length equal to about the width of 12 fingers.

Characterization of metastatic intestinal adenocarcinoma with differentiation into multiple morphologic cell types in a Virginia opossum. (1/188)

A captively maintained mature male opossum (Didelphis virginiana) utilized in a research protocol was presented with clinical signs of chronic diarrhea and severe muscle wasting. At necropsy, there was multifocal mural gastric, intestinal, and urinary bladder thickening, concurrent bilateral hydroureter and hydronephrosis, and extensive fibrous abdominal adhesions. Histologic evaluation revealed intestinal adenocarcinoma with coelomic metastasis to the stomach and urinary bladder. The adenocarcinoma was evaluated using histochemistry and electron microscopy. Paneth, enteroendocrine, and goblet cell differentiation was documented in primary and metastatic sites. This unique presentation of intestinal adenocarcinoma has not previously been reported in the opossum or any other animals. Intestinal neoplasia with Paneth cell differentiation is extremely rare and has been reported in humans with familial adenomatous polyposis.  (+info)

Regulation of intestinal alpha-defensin activation by the metalloproteinase matrilysin in innate host defense. (2/188)

Precursors of alpha-defensin peptides require activation for bactericidal activity. In mouse small intestine, matrilysin colocalized with alpha-defensins (cryptdins) in Paneth cell granules, and in vitro it cleaved the pro segment from cryptdin precursors. Matrilysin-deficient (MAT-/-) mice lacked mature cryptdins and accumulated precursor molecules. Intestinal peptide preparations from MAT-/- mice had decreased antimicrobial activity. Orally administered bacteria survived in greater numbers and were more virulent in MAT-/- mice than in MAT+/+ mice. Thus, matrilysin functions in intestinal mucosal defense by regulating the activity of defensins, which may be a common role for this metalloproteinase in its numerous epithelial sites of expression.  (+info)

Peptide localization and gene structure of cryptdin 4, a differentially expressed mouse paneth cell alpha-defensin. (3/188)

Paneth cells in crypts of the small intestine express antimicrobial peptides, including alpha-defensins, termed cryptdins in mice. Of the known Paneth cell alpha-defensins, the cryptdin 4 gene is unique, because it is inactive in the duodenum and expressed at maximal levels in the distal small bowel (D. Darmoul and A. J. Ouellette, Am. J. Physiol. 271:G68-G74, 1996). With a cryptdin 4-specific antibody, immunohistochemical staining of ileal Paneth cells was strong and specific for cytoplasmic granules, demonstrating that this microbicidal peptide is a secretory product of Paneth cells in the distal small intestine. Consistent with the pattern of cryptdin 4 mRNA distribution along the length of the gut, the cryptdin 4 peptide was not detected in duodenum. Structurally, the cryptdin 4 gene resembles other Paneth cell alpha-defensin genes. Its two exons, transcriptional start site, intron, splice sites, and 3' flanking sequences are characteristic of the highly conserved mouse alpha-defensin genes. However, in the region upstream of the transcriptional initiation site, the cryptdin 4 gene contains a repeated 130-bp element that is unique to this alpha-defensin gene. Every independent cryptdin 4 genomic clone examined carries the repeated element, which contains putative recognition sequences for TF-IID-EIIA, cMyc-RS-1, and IgHC.2/CuE1.1; the repeat proximal to the start of transcription replaces DNA at the corresponding position in other mouse alpha-defensin genes. We speculate that this unique duplicated element may have a cis-acting regulatory role in the positional specificity of cryptdin 4 gene expression.  (+info)

Selective sparing of goblet cells and paneth cells in the intestine of methotrexate-treated rats. (4/188)

Proliferation, differentiation, and cell death were studied in small intestinal and colonic epithelia of rats after treatment with methotrexate. Days 1-2 after treatment were characterized by decreased proliferation, increased apoptosis, and decreased numbers and depths of small intestinal crypts in a proximal-to-distal decreasing gradient along the small intestine. The remaining crypt epithelium appeared flattened, except for Paneth cells, in which lysozyme protein and mRNA expression was increased. Regeneration through increased proliferation during days 3-4 coincided with villus atrophy, showing decreased numbers of villus enterocytes and decreased expression of the enterocyte-specific genes sucrase-isomaltase and carbamoyl phosphate synthase I. Remarkably, goblet cells were spared at villus tips and remained functional, displaying Muc2 and trefoil factor 3 expression. On days 8-10, all parameters had returned to normal in the whole small intestine. No methotrexate-induced changes were seen in epithelial morphology, proliferation, apoptosis, Muc2, and TFF3 immunostaining in the colon. The observed small intestinal sparing of Paneth cells and goblet cells following exposure to methotrexate is likely to contribute to epithelial defense during increased vulnerability of the intestinal epithelium.  (+info)

The antibacterial properties of secreted phospholipases A(2). (5/188)

There is a considerable body of evidence to support the antibacterial properties of the group IIa phospholipase A(2) as an important physiological function. This enzyme is able to act as an acute phase protein and may be part of the innate defence system of the body, acting in concert with other antibacterial proteins and peptides. The enzyme is most effective against Gram-positive bacteria whereas penetration of the lipopolysaccharide coat of Gram-negative bacteria requires bactericidal/permeability-increasing protein (BPI) as an additional permeabilizing factor. The global cationic nature of this protein (pI>10.5) appears to facilitate penetration of the anionic bacterial cell wall. In addition, the considerable preference of the enzyme for anionic phospholipid interfaces provides specificity toward anionic bacterial membranes as opposed to zwitterionic eucaryotic cell membranes.  (+info)

Human defensin 5 is stored in precursor form in normal Paneth cells and is expressed by some villous epithelial cells and by metaplastic Paneth cells in the colon in inflammatory bowel disease. (6/188)

BACKGROUND AND AIMS: Intestinal epithelial cell derived antimicrobial peptides of the defensin family may play a major role in host defence against microorganisms. Our aims were to (i) isolate, characterise, and investigate the processing of human defensin 5 (HD-5) in normal Paneth cells and (ii) investigate expression of HD-5 in active inflammatory bowel disease (IBD). METHODS: Antiserum raised against chemically synthesised putative mature HD-5 was used for immunohistochemistry and purification of HD-5 from extracts of normal terminal ileal crypts. RESULTS: In normal and Crohn's disease terminal ileum, HD-5 immunoreactivity was seen in Paneth cells and in some villous epithelial cells. Normal colonic mucosa did not express HD-5 but HD-5 immunoreactivity was seen in cells in the colonic crypt region of many IBD samples. N-terminal amino acid sequence analysis of HD-5 purified from normal terminal ileal Paneth cells consistently showed the predicted sequence of the precursor form of the peptide. Following stimulation of isolated intact normal terminal ileal crypts, a truncated form of HD-5, with the N-terminal sequence GEDNQLAIS, was detected in the supernatant. CONCLUSIONS: (i) HD-5 is present only in the precursor form in normal terminal ileal Paneth cells and is processed to the mature form during and/or after secretion, (ii) some villous epithelial cells express HD-5, and (iii) HD-5 is expressed by metaplastic Paneth cells in the colon in IBD.  (+info)

Identification of xanthine dehydrogenase/xanthine oxidase as a rat Paneth cell zinc-binding protein. (7/188)

Paneth cells are zinc-containing cells localized in small intestinal crypts, but their function has not been fully elucidated. Previously, we showed that an intravenous injection of diphenylthiocarbazone (dithizone), a zinc chelator, induced selective killing of Paneth cells, and purified a zinc-binding protein in Paneth cells. In the present study, we further characterized one of these proteins, named zinc-binding protein of Paneth cells (ZBPP)-1. Partial amino acid sequences of ZBPP-1 showed identity with rat xanthine dehydrogenase (XD)/xanthine oxidase (XO). Anti-rat XD antibody (Ab) recognized ZBPP-1, and conversely anti ZBPP-1 Ab recognized 85 kDa fragment of rat XD in Western blotting. Messenger RNA and protein levels of XD were consistent with our previous data on the fluctuation of Paneth cell population after dithizone injection. Thus, ZBPP-1 is an 85 kDa fragment of XD/XO in Paneth cells. XD/XO in Paneth cells may play important roles in intestinal function.  (+info)

Mucosal T cells regulate Paneth and intermediate cell numbers in the small intestine of T. spiralis-infected mice. (8/188)

Secretions of Paneth, intermediate and goblet cells have been implicated in innate intestinal host defense. We have investigated the role of T cells in effecting alterations in small intestinal epithelial cell populations induced by infection with the nematode Trichinella spiralis. Small intestinal tissue sections from euthymic and athymic (nude) mice, and mice with combined deficiency in T-cell receptor beta and delta genes [TCR(beta/delta)-/-] infected orally with T. spiralis larvae, were examined by electron microscopy and after histochemical and lineage-specific immunohistochemical staining. Compared with uninfected controls, Paneth and intermediate cell numbers increased significantly in infected euthymic and nude mice but not infected TCR(beta/delta)-/- mice. Transfer of mesenteric lymph node cells before infection led to an increase in Paneth and intermediate cells in TCR(beta/delta)-/- mice. In infected euthymic mice, Paneth cells and intermediate cells expressed cryptdins (alpha-defensins) but not intestinal trefoil factor (ITF), and goblet cells expressed ITF but not cryptdins. In conclusion, a unique, likely thymic-independent population of mucosal T cells modulates innate small intestinal host defense in mice by increasing the number of Paneth and intermediate cells in response to T. spiralis infection.  (+info)

Paneth cells are specialized epithelial cells located in the small intestine, specifically in the crypts of Lieberkühn. They play an essential role in the immune function and maintenance of the intestinal environment. Paneth cells are characterized by their large, granulated secretory vesicles that contain antimicrobial peptides and proteins, such as defensins and lysozyme. These substances help to control the growth of bacteria in the small intestine and maintain a balanced microbiota. Additionally, Paneth cells secrete other factors that support the function and survival of stem cells located in the crypts. They are also involved in the inflammatory response by producing cytokines and chemokines, which help to recruit immune cells to the site of infection or injury.

Alpha-defensins are a type of defensin, which are small cationic host defense peptides that contribute to the innate immune system's response to microbial invasion. They are primarily produced by neutrophils, but can also be expressed by some epithelial cells and other immune cells. Alpha-defensins have broad-spectrum antimicrobial activity against bacteria, fungi, and enveloped viruses. They also play a role in modulating the inflammatory response and wound healing. There are six human alpha-defensin genes (DEFA1 to DEFA6) that encode six different peptides: Human Neutrophil Peptides 1-4 (HNP1-4) and Human Defensin 5 and 6 (HD5 and HD6). The HNPs are stored in the azurophilic granules of neutrophils and are released upon their activation, while HD5 and HD6 are found in the Paneth cells of the small intestine.

Dithizone is a chemical compound with the formula (C6H5N2S)2Cu. It is a dark red solid that is soluble in organic solvents and has a range of uses in chemistry and biology, including as a complexing agent for metal ions and as a histochemical stain.

In medicine, dithizone has been used in the past as a diagnostic aid to detect heavy metal poisoning, such as lead or mercury, by forming colored complexes with these metals that can be detected in urine or feces. However, its use as a diagnostic tool is not widespread today due to the availability of safer and more reliable tests.

It's important to note that dithizone is toxic and should only be handled by trained professionals wearing appropriate personal protective equipment.

The small intestine is the portion of the gastrointestinal tract that extends from the pylorus of the stomach to the beginning of the large intestine (cecum). It plays a crucial role in the digestion and absorption of nutrients from food. The small intestine is divided into three parts: the duodenum, jejunum, and ileum.

1. Duodenum: This is the shortest and widest part of the small intestine, approximately 10 inches long. It receives chyme (partially digested food) from the stomach and begins the process of further digestion with the help of various enzymes and bile from the liver and pancreas.
2. Jejunum: The jejunum is the middle section, which measures about 8 feet in length. It has a large surface area due to the presence of circular folds (plicae circulares), finger-like projections called villi, and microvilli on the surface of the absorptive cells (enterocytes). These structures increase the intestinal surface area for efficient absorption of nutrients, electrolytes, and water.
3. Ileum: The ileum is the longest and final section of the small intestine, spanning about 12 feet. It continues the absorption process, mainly of vitamin B12, bile salts, and any remaining nutrients. At the end of the ileum, there is a valve called the ileocecal valve that prevents backflow of contents from the large intestine into the small intestine.

The primary function of the small intestine is to absorb the majority of nutrients, electrolytes, and water from ingested food. The mucosal lining of the small intestine contains numerous goblet cells that secrete mucus, which protects the epithelial surface and facilitates the movement of chyme through peristalsis. Additionally, the small intestine hosts a diverse community of microbiota, which contributes to various physiological functions, including digestion, immunity, and protection against pathogens.

Defensins are small, cationic host defense peptides that contribute to the innate immune system's response against microbial pathogens. They are produced by various cell types, including neutrophils, epithelial cells, and some bone marrow-derived cells. Defensins have a broad spectrum of antimicrobial activity against bacteria, fungi, viruses, and enveloped lipid bilayers.

Defensins are classified into two main groups: α-defensins and β-defensins. Human α-defensins include human neutrophil peptides (HNP) 1-4 and human defensin 5, 6 (HD5, HD6). These are primarily produced by neutrophils and Paneth cells in the small intestine. β-defensins, on the other hand, are produced by various epithelial cells throughout the body.

Defensins work by disrupting the microbial membrane's integrity, leading to cell lysis and death. They also have immunomodulatory functions, such as chemotaxis of immune cells, modulation of cytokine production, and enhancement of adaptive immune responses. Dysregulation of defensin expression has been implicated in several diseases, including inflammatory bowel disease, chronic obstructive pulmonary disease, and certain skin disorders.

The intestinal mucosa is the innermost layer of the intestines, which comes into direct contact with digested food and microbes. It is a specialized epithelial tissue that plays crucial roles in nutrient absorption, barrier function, and immune defense. The intestinal mucosa is composed of several cell types, including absorptive enterocytes, mucus-secreting goblet cells, hormone-producing enteroendocrine cells, and immune cells such as lymphocytes and macrophages.

The surface of the intestinal mucosa is covered by a single layer of epithelial cells, which are joined together by tight junctions to form a protective barrier against harmful substances and microorganisms. This barrier also allows for the selective absorption of nutrients into the bloodstream. The intestinal mucosa also contains numerous lymphoid follicles, known as Peyer's patches, which are involved in immune surveillance and defense against pathogens.

In addition to its role in absorption and immunity, the intestinal mucosa is also capable of producing hormones that regulate digestion and metabolism. Dysfunction of the intestinal mucosa can lead to various gastrointestinal disorders, such as inflammatory bowel disease, celiac disease, and food allergies.

Muramidase, also known as lysozyme, is an enzyme that hydrolyzes the glycosidic bond between N-acetylmuramic acid and N-acetylglucosamine in peptidoglycan, a polymer found in bacterial cell walls. This enzymatic activity plays a crucial role in the innate immune system by contributing to the destruction of invading bacteria. Muramidase is widely distributed in various tissues and bodily fluids, such as tears, saliva, and milk, and is also found in several types of white blood cells, including neutrophils and monocytes.

Matrix metalloproteinase 7 (MMP-7), also known as matrilysin, is a type of enzyme that belongs to the matrix metalloproteinase family. These enzymes are capable of degrading various components of the extracellular matrix, which is the structural framework of tissues in the body. MMP-7 has a broad range of substrates and can break down proteins such as collagens, gelatins, and caseins, as well as other matrix proteins. It plays important roles in tissue remodeling, wound healing, and cell migration, among other processes.

MMP-7 is synthesized and secreted by various cells, including epithelial cells, fibroblasts, and immune cells. It is a small enzyme with a molecular weight of around 28 kDa and is secreted in an active form, unlike many other MMPs that are secreted as inactive proenzymes and require activation by other proteases.

Increased expression of MMP-7 has been implicated in several pathological conditions, including cancer, where it can contribute to tumor invasion and metastasis by degrading the extracellular matrix and releasing growth factors. It has also been associated with inflammatory diseases such as rheumatoid arthritis and periodontitis.

The intestines, also known as the bowel, are a part of the digestive system that extends from the stomach to the anus. They are responsible for the further breakdown and absorption of nutrients from food, as well as the elimination of waste products. The intestines can be divided into two main sections: the small intestine and the large intestine.

The small intestine is a long, coiled tube that measures about 20 feet in length and is lined with tiny finger-like projections called villi, which increase its surface area and enhance nutrient absorption. The small intestine is where most of the digestion and absorption of nutrients takes place.

The large intestine, also known as the colon, is a wider tube that measures about 5 feet in length and is responsible for absorbing water and electrolytes from digested food, forming stool, and eliminating waste products from the body. The large intestine includes several regions, including the cecum, colon, rectum, and anus.

Together, the intestines play a critical role in maintaining overall health and well-being by ensuring that the body receives the nutrients it needs to function properly.

Goblet cells are specialized epithelial cells that are located in various mucosal surfaces, including the respiratory and gastrointestinal tracts. They are named for their goblet-like shape, which is characterized by a narrow base and a wide, rounded top that contains secretory granules. These cells play an essential role in producing and secreting mucins, which are high molecular weight glycoproteins that form the gel-like component of mucus.

Mucus serves as a protective barrier for the underlying epithelial cells by trapping foreign particles, microorganisms, and toxins, preventing them from coming into contact with the epithelium. Goblet cells also help maintain the hydration of the mucosal surface, which is important for normal ciliary function in the respiratory tract and for the movement of food through the gastrointestinal tract.

In summary, goblet cells are secretory cells that produce and release mucins to form the mucus layer, providing a protective barrier and maintaining the homeostasis of mucosal surfaces.

Ileitis is a medical term that refers to inflammation of the ileum, which is the last part of the small intestine. The condition can have various causes, including infections, autoimmune disorders, and inflammatory bowel diseases such as Crohn's disease.

The symptoms of ileitis may include abdominal pain, diarrhea, fever, weight loss, and nausea or vomiting. The diagnosis of ileitis typically involves a combination of medical history, physical examination, laboratory tests, and imaging studies such as CT scans or MRI.

Treatment for ileitis depends on the underlying cause of the inflammation. In cases of infectious ileitis, antibiotics may be used to treat the infection. For autoimmune or inflammatory causes, medications that suppress the immune system may be necessary to reduce inflammation and manage symptoms.

In severe cases of ileitis, surgery may be required to remove damaged portions of the intestine or to drain abscesses. It is important to seek medical attention if you experience symptoms of ileitis, as early diagnosis and treatment can help prevent complications and improve outcomes.

The ileum is the third and final segment of the small intestine, located between the jejunum and the cecum (the beginning of the large intestine). It plays a crucial role in nutrient absorption, particularly for vitamin B12 and bile salts. The ileum is characterized by its thin, lined walls and the presence of Peyer's patches, which are part of the immune system and help surveil for pathogens.

Crohn's disease is a type of inflammatory bowel disease (IBD) that can affect any part of the gastrointestinal tract, from the mouth to the anus. It is characterized by chronic inflammation of the digestive tract, which can lead to symptoms such as abdominal pain, diarrhea, fatigue, weight loss, and malnutrition.

The specific causes of Crohn's disease are not fully understood, but it is believed to be related to a combination of genetic, environmental, and immune system factors. The disease can affect people of any age, but it is most commonly diagnosed in young adults between the ages of 15 and 35.

There is no cure for Crohn's disease, but treatments such as medications, lifestyle changes, and surgery can help manage symptoms and prevent complications. Treatment options depend on the severity and location of the disease, as well as the individual patient's needs and preferences.

Protein precursors, also known as proproteins or prohormones, are inactive forms of proteins that undergo post-translational modification to become active. These modifications typically include cleavage of the precursor protein by specific enzymes, resulting in the release of the active protein. This process allows for the regulation and control of protein activity within the body. Protein precursors can be found in various biological processes, including the endocrine system where they serve as inactive hormones that can be converted into their active forms when needed.

Intestinal neoplasms refer to abnormal growths in the tissues of the intestines, which can be benign or malignant. These growths are called neoplasms and they result from uncontrolled cell division. In the case of intestinal neoplasms, these growths occur in the small intestine, large intestine (colon), rectum, or appendix.

Benign intestinal neoplasms are not cancerous and often do not invade surrounding tissues or spread to other parts of the body. However, they can still cause problems if they grow large enough to obstruct the intestines or cause bleeding. Common types of benign intestinal neoplasms include polyps, leiomyomas, and lipomas.

Malignant intestinal neoplasms, on the other hand, are cancerous and can invade surrounding tissues and spread to other parts of the body. The most common type of malignant intestinal neoplasm is adenocarcinoma, which arises from the glandular cells lining the inside of the intestines. Other types of malignant intestinal neoplasms include lymphomas, sarcomas, and carcinoid tumors.

Symptoms of intestinal neoplasms can vary depending on their size, location, and type. Common symptoms include abdominal pain, bloating, changes in bowel habits, rectal bleeding, weight loss, and fatigue. If you experience any of these symptoms, it is important to seek medical attention promptly.

Intestinal diseases refer to a wide range of conditions that affect the function or structure of the small intestine, large intestine (colon), or both. These diseases can cause various symptoms such as abdominal pain, diarrhea, constipation, bloating, nausea, vomiting, and weight loss. They can be caused by infections, inflammation, genetic disorders, or other factors. Some examples of intestinal diseases include inflammatory bowel disease (IBD), irritable bowel syndrome (IBS), celiac disease, Crohn's disease, ulcerative colitis, and intestinal infections. The specific medical definition may vary depending on the context and the specific condition being referred to.

Enteroendocrine cells are specialized cells found within the epithelial lining of the gastrointestinal tract, which play a crucial role in regulating digestion and energy balance. They are responsible for producing and secreting various hormones in response to mechanical or chemical stimuli, such as the presence of nutrients in the gut lumen. These hormones include:

1. Gastrin: Secreted by G cells in the stomach, gastrin promotes the release of hydrochloric acid from parietal cells and increases gastric motility.
2. Cholecystokinin (CCK): Produced by I cells in the small intestine, CCK stimulates the secretion of digestive enzymes from the pancreas, promotes gallbladder contraction, and inhibits gastric emptying.
3. Secretin: Released by S cells in the duodenum, secretin stimulates bicarbonate secretion from the pancreas to neutralize stomach acid and increases pancreatic secretions.
4. Serotonin (5-HT): Found in enterochromaffin cells throughout the gastrointestinal tract, serotonin regulates gut motility, sensation, and secretion. It also plays a role in modulating the immune response and affecting mood and cognition when released into the bloodstream.
5. Motilin: Produced by MO cells in the small intestine, motilin stimulates gastrointestinal motility and regulates the migrating motor complex (MMC), which is responsible for the housekeeping functions of the gut during fasting periods.
6. Gastric inhibitory peptide (GIP): Secreted by K cells in the duodenum, GIP promotes insulin secretion, inhibits gastric acid secretion, and stimulates intestinal motility and pancreatic bicarbonate secretion.
7. Glucagon-like peptide-1 (GLP-1) and glucagon-like peptide-2 (GLP-2): Released by L cells in the ileum and colon, GLP-1 stimulates insulin secretion, inhibits glucagon release, slows gastric emptying, and promotes satiety. GLP-2 enhances intestinal growth and absorption.

These hormones play crucial roles in regulating various aspects of gastrointestinal function, including digestion, motility, secretion, sensation, and immune response. Dysregulation of these hormones can contribute to the development of several gastrointestinal disorders, such as irritable bowel syndrome (IBS), inflammatory bowel disease (IBD), functional dyspepsia, and diabetes. Understanding the complex interactions between these hormones and their receptors is essential for developing targeted therapeutic strategies to treat gastrointestinal diseases.

Beta-defensins are a group of small, cationic host defense peptides that play an important role in the innate immune system. They have broad-spectrum antimicrobial activity against various pathogens, including bacteria, fungi, and viruses. Beta-defensins are produced by epithelial cells, phagocytes, and other cell types in response to infection or inflammation. They function by disrupting the membranes of microbes, leading to their death. Additionally, beta-defensins can also modulate the immune response by recruiting immune cells to the site of infection and regulating inflammation. Mutations in beta-defensin genes have been associated with increased susceptibility to infectious diseases.

The large intestine, also known as the colon, is the lower part of the gastrointestinal tract that extends from the cecum, where it joins the small intestine, to the anus. It is called "large" because it has a larger diameter compared to the small intestine and is responsible for several important functions in the digestive process.

The large intestine measures about 1.5 meters (5 feet) long in adults and consists of four main regions: the ascending colon, transverse colon, descending colon, and sigmoid colon. The primary function of the large intestine is to absorb water and electrolytes from undigested food materials, compact the remaining waste into feces, and store it until it is eliminated through defecation.

The large intestine also contains a diverse population of bacteria that aid in digestion by breaking down complex carbohydrates, producing vitamins like vitamin K and some B vitamins, and competing with harmful microorganisms to maintain a healthy balance within the gut. Additionally, the large intestine plays a role in immune function and helps protect the body from pathogens through the production of mucus, antimicrobial substances, and the activation of immune cells.

The appendix is a small, tube-like structure that projects from the large intestine, located in the lower right quadrant of the abdomen. Its function in humans is not well understood and is often considered vestigial, meaning it no longer serves a necessary purpose. However, in some animals, the appendix plays a role in the immune system. Inflammation of the appendix, known as appendicitis, can cause severe abdominal pain and requires medical attention, often leading to surgical removal of the appendix (appendectomy).

Cytoplasmic granules are small, membrane-bound organelles or inclusions found within the cytoplasm of cells. They contain various substances such as proteins, lipids, carbohydrates, and genetic material. Cytoplasmic granules have diverse functions depending on their specific composition and cellular location. Some examples include:

1. Secretory granules: These are found in secretory cells and store hormones, neurotransmitters, or enzymes before they are released by exocytosis.
2. Lysosomes: These are membrane-bound organelles that contain hydrolytic enzymes for intracellular digestion of waste materials, foreign substances, and damaged organelles.
3. Melanosomes: Found in melanocytes, these granules produce and store the pigment melanin, which is responsible for skin, hair, and eye color.
4. Weibel-Palade bodies: These are found in endothelial cells and store von Willebrand factor and P-selectin, which play roles in hemostasis and inflammation.
5. Peroxisomes: These are single-membrane organelles that contain enzymes for various metabolic processes, such as β-oxidation of fatty acids and detoxification of harmful substances.
6. Lipid bodies (also called lipid droplets): These are cytoplasmic granules that store neutral lipids, such as triglycerides and cholesteryl esters. They play a role in energy metabolism and intracellular signaling.
7. Glycogen granules: These are cytoplasmic inclusions that store glycogen, a polysaccharide used for energy storage in animals.
8. Protein bodies: Found in plants, these granules store excess proteins and help regulate protein homeostasis within the cell.
9. Electron-dense granules: These are found in certain immune cells, such as mast cells and basophils, and release mediators like histamine during an allergic response.
10. Granules of unknown composition or function may also be present in various cell types.

Necrotizing enterocolitis (NEC) is a serious gastrointestinal condition that primarily affects premature infants. It is characterized by the inflammation and death of intestinal tissue, which can lead to perforations (holes) in the bowel wall. Here's a brief medical definition:

Necrotizing enterocolitis (NEK-roh-tiz-ing en-ter-koh-li-TIE-tis): A gastrointestinal emergency in which the inner lining of the intestinal wall undergoes necrosis (tissue death) due to inflammation, often affecting premature infants. The condition may result in bowel perforations, sepsis, and other systemic complications, requiring surgical intervention and intensive care management.

The exact cause of NEC is not fully understood, but it's thought to be associated with factors such as prematurity, formula feeding, intestinal immaturity or injury, and disturbed blood flow in the intestines. Symptoms may include abdominal distention, bloody stools, feeding intolerance, lethargy, and temperature instability. Early recognition and prompt treatment are crucial for improving outcomes in affected infants.

The jejunum is the middle section of the small intestine, located between the duodenum and the ileum. It is responsible for the majority of nutrient absorption that occurs in the small intestine, particularly carbohydrates, proteins, and some fats. The jejunum is characterized by its smooth muscle structure, which allows it to contract and mix food with digestive enzymes and absorb nutrients through its extensive network of finger-like projections called villi.

The jejunum is also lined with microvilli, which further increase the surface area available for absorption. Additionally, the jejunum contains numerous lymphatic vessels called lacteals, which help to absorb fats and fat-soluble vitamins into the bloodstream. Overall, the jejunum plays a critical role in the digestion and absorption of nutrients from food.

Acrodermatitis is a term that describes several inflammatory skin conditions characterized by redness, swelling, and blistering that typically affect the hands, feet, and face. The medical definition of acrodermatitis includes various subtypes, each with its own specific causes and symptoms. Here are some of the most common forms of acrodermatitis:

1. Acrodermatitis enteropathica: A rare inherited disorder caused by a deficiency in zinc absorption. Symptoms include redness, swelling, blistering, and crusting around the mouth, eyes, and genitals, as well as the hands and feet.
2. Acrodermatitis continua of Hallopeau: A rare chronic inflammatory skin condition that affects the fingertips and toes. Symptoms include redness, swelling, blistering, and crusting, which can lead to nail deformities and loss.
3. Gianotti-Crosti syndrome (acrodermatitis papulosa): A viral exanthem that typically affects children between 6 months and 15 years of age. Symptoms include red, raised bumps on the face, buttocks, and extremities, which can be itchy and painful.
4. Pustular acrodermatitis: A rare skin condition characterized by pustules (pus-filled bumps) that form on the palms of the hands and soles of the feet. Symptoms may also include fever, chills, and fatigue.
5. Infantile acrodermatitis: A rare inflammatory skin disorder that affects infants and young children. Symptoms include redness, swelling, and blistering around the mouth, eyes, and genitals, as well as the hands and feet.

Treatment for acrodermatitis depends on the underlying cause of the condition. In some cases, topical creams or ointments may be sufficient to manage symptoms, while in others, systemic treatments such as antibiotics or immunosuppressive drugs may be necessary.

NOD2 (Nucleotide-binding Oligomerization Domain-containing protein 2) signaling adaptor protein, also known as CARD15 (Caspase Recruitment Domain-containing protein 15), is a crucial intracellular pattern recognition receptor (PRR) that plays an essential role in the innate immune response. NOD2 is primarily expressed in monocytes, macrophages, dendritic cells, and intestinal epithelial cells.

NOD2 signaling adaptor protein contains two caspase recruitment domains (CARD), a nucleotide-binding oligomerization domain (NOD), and multiple leucine-rich repeats (LRR). The LRR region is responsible for recognizing and binding to pathogen-associated molecular patterns (PAMPs) derived from bacterial cell walls, such as muramyl dipeptide (MDP). Upon recognition of MDP, NOD2 undergoes oligomerization through its NOD domain, which leads to the recruitment of receptor-interacting protein kinase 2 (RIPK2) via CARD-CARD interactions. This interaction results in the activation of downstream signaling pathways, including nuclear factor kappa B (NF-κB) and mitogen-activated protein kinases (MAPKs), which ultimately induce the expression of proinflammatory cytokines, chemokines, and antimicrobial peptides.

Dysregulation or mutations in NOD2 signaling adaptor protein have been implicated in several inflammatory diseases, such as Crohn's disease, Blau syndrome, and susceptibility to certain mycobacterial infections.

The duodenum is the first part of the small intestine, immediately following the stomach. It is a C-shaped structure that is about 10-12 inches long and is responsible for continuing the digestion process that begins in the stomach. The duodenum receives partially digested food from the stomach through the pyloric valve and mixes it with digestive enzymes and bile produced by the pancreas and liver, respectively. These enzymes help break down proteins, fats, and carbohydrates into smaller molecules, allowing for efficient absorption in the remaining sections of the small intestine.

... it has been shown that Paneth cells clear dying cells via apoptotic cell uptake. The pahgocytic function of Paneth cells was ... Paneth cells are named after 19th-century pathologist Joseph Paneth. Paneth cells are found throughout the small intestine and ... Paneth cells are cells in the small intestine epithelium, alongside goblet cells, enterocytes, and enteroendocrine cells. Some ... There are on average 5-12 Paneth cells in each small intestinal crypt. Unlike the other epithelial cell types, Paneth cells ...
Paneth cells answers are found in the Tabers Medical Dictionary powered by Unbound Medicine. Available for iPhone, iPad, ... "Paneth Cells." Tabers Medical Dictionary, 24th ed., F.A. Davis Company, 2021. Tabers Online, www.tabers.com/tabersonline/view ... Dictionary/729186/all/Paneth_cells. Paneth cells. In: Venes DD, ed. Tabers Medical Dictionary. F.A. Davis Company; 2021. https ... Paneth Cells [Internet]. In: Venes DD, editors. Tabers Medical Dictionary. F.A. Davis Company; 2021. [cited 2023 December 08 ...
Paneth cells, Tuft cells, and even stem cells. Thus, IL-22 does not directly control the regenerative capacity of crypt stem ... Optimized human intestinal organoid model reveals interleukin-22-dependency of paneth cell formation, Cell Stem Cell 29, (9), ... cells but rather boosts Paneth cell numbers, as well as the expression of AMPs in all cell types. ... Optimized human intestinal organoid model reveals interleukin-22-dependency of paneth cell formation Back to all publications ...
Maturation and positioning of goblet cells and Paneth cells, the main cell lineage of the intestinal innate immune system, was ... A key role for E-cadherin in intestinal homeostasis and Paneth cell maturation. In: PLOS ONE 5(12), e14325 [PDF, 21MB] ... epithelial lining by providing mechanical integrity and is a prerequisite for the proper maturation of Paneth and goblet cells. ... Loss of E-cadherin led cells migrate faster along the crypt-villus axis and perturbed cellular differentiation. ...
Paneth Cell Specific) ELISA Kit from Gentaur Elisa Kits. Cat Number: G-EC-04309. USA, UK & Europe Distribution. ... Mouse DEFa5 (Defensin Alpha 5, Paneth Cell Specific) ELISA Kit , G-EC-04309. Gentaur Elisa ... Mouse DEFa5 (Defensin Alpha 5, Paneth Cell Specific) ELISA Kit , G-EC-04309 ... Mouse DEFa5 (Defensin Alpha 5, Paneth Cell Specific) ELISA Kit , G-EC-04309 , Gentaur Elisa Kits ...
Crypts begin to form around day 7 of postnatal mice (P7), and Paneth cells usually appear within the first 2 weeks. Paneth cell ... Paneth cells are antimicrobial peptide-secreting epithelial cells located at the bottom of the intestinal crypts of Lieberk& ... The epithelium consists of absorptive cells (or enterocytes), goblet cells, enteroendocrine cells, tuft cells, and Paneth cells ... there were Paneth cells in addition to goblet cells and two types of granular goblet cells (Fig. 8a). However, Paneth cells ...
Paneth cells, enteroendocrine cells, tuft cells, and stem cells. In contrast, the lamina propria is composed of immune cells ... it has been shown that Paneth cells clear dying cells via apoptotic cell uptake. The pahgocytic function of Paneth cells was ... Paneth cells are cells in the small intestine epithelium, alongside goblet cells, enterocytes, and enteroendocrine cells.[1] ... Paneth cells originate at the stem cell region near the bottom of the gland.[4] There are on average 5-12 Paneth cells in each ...
Most farm animals possess Paneth cells in their small intestine, as identified by various staining methods, and Paneth cells of ... In small intestine, Paneth cells are well known for their regulation of intestinal microbiota and intestinal stem cells (ISCs ... Paneth cells in farm animals and their antimicrobial peptides (AMPs) are susceptible to multiple factors such as dietary ... This review first summarizes the current status of Paneth cells in pig, cattle, sheep, horse, chicken and rabbit, and points ...
... is highly expressed by intestinal stem cells and controls the size of the intestinal stem-cell niche by regulating the ... Intestinal stem-cell maintenance has so far been attributed to a combination of Wnt and Notch activation and Bmpr inhibition11, ... Maintenance of adult tissues is carried out by stem cells and is sustained throughout life in a highly ordered manner1,2. ... Thus, ErbB activation acts in concert with Wnt, Notch and Bmpr inhibition, to modulate stem-cell proliferation in the crypt. ...
Paneth cells. As shown in Table 1, 392 genes are elevated in paneth cells compared to other cell types. Paneth cells are ... Club cells. As shown in Table 1, 177 genes are elevated in club cells compared to other cell types. Club cells (also called ... Ciliated cells. As shown in Table 1, 534 genes are elevated in ciliated cells compared to other cell types. Ciliated cells with ... 297 genes are elevated in basal respiratory cells compared to other cell types. Basal cells are small stem cells located in the ...
Paneth cell depleted mice small intestine B) control mice small intestine with Paneth cells. Nuclei (blue), Paneth cells (Green ... were significantly decreased in Paneth cell depleted mice after PPVL. In the absence of Paneth cells, proteomic analyses showed ... Lymphatic vessels, Lyve-1, Paneth cells. Each article is made available under the terms of the Creative Commons Attribution-Non ... Regulation of Lymphangiogenesis by Paneth Cells in Normal Physiology and Experimental Portal Hypertension. 2 Mins ...
The results of the study were published on 23 August in Cell Stem Cell. ... Specifically, the researchers managed to develop organoids that contain mature Paneth cells, which were not present in the ... Missing Paneth cells. The small intestine contains a wide variety of cells, such as enterocytes, stem cells and Paneth cells. ... www.cell.com/cell-stem-cell/fu … 1934-5909(22)00338-1 Journal information: Cell Stem Cell. , Nature. ...
Adenocarcinoma with Paneth cell NE differentiation; 3) Carcinoid tumor; 4) Small cell carcinoma; 5) Large cell NE carcinoma; ... The article also highlights "prostate carcinoma with overlapping features of small cell carcinoma and acinar adenocarcinoma" ... and "castrate-resistant prostate cancer with small cell cancer-like clinical presentation". It is envisioned that specific ...
Transfer of mesenteric lymph node cells before infection led to an increase in Paneth and intermediate cells in TCR(beta/delta ... In infected euthymic mice, Paneth cells and intermediate cells expressed cryptdins (alpha-defensins) but not intestinal trefoil ... Compared with uninfected controls, Paneth and intermediate cell numbers increased significantly in infected euthymic and nude ... T cells modulates innate small intestinal host defense in mice by increasing the number of Paneth and intermediate cells in ...
In vitro generation and stimulation of Paneth cell (PC)-like cells. Paneth cell (PC)-like cells were generated by treatment of ... we used the Paneth cell (PC)-like cells induced as previous methods [35, 36], serving as the functional model of Paneth cells, ... Paneth cells are specialized epithelial cells that function as resident host-defense cells by secreting various mediators [28 ... to investigate the mechanism by which NOD2 may regulate IL-23p19 expression in Paneth cells, since primary Paneth cells do not ...
... mostly characteristic of Paneth and goblet cells, in addition to other changes that may resemble Crohns disease. ... cells. Asthma patients (n = 15) and controls (n = 15) had similar age (p = 0.967), body mass index (p = 0.870), similar numbers ... and not in any other cell/tissue types. More genes were found to be overexpressed (1,150) than under-expressed (380). The most ... as well as Paneth or crypt cells. Taken as a whole, these results potentially demonstrate stimulation of Paneth cells, likely ...
Paneth cells constitute the niche for Lgr5 stem cells in intestinal crypts p.415 doi: 10.1038/nature09637 ... Evolution of human BCR-ABL1 lymphoblastic leukaemia-initiating cells p.362 doi: 10.1038/nature09733 ... Genetic variegation of clonal architecture and propagating cells in leukaemia p.356 doi: 10.1038/nature09650 ... Preplay of future place cell sequences by hippocampal cellular assemblies p.397 doi: 10.1038/nature09633 ...
Some cases have increased Paneth cells (Siders, 1992). View Media Gallery Postradiation Therapy Pathology of Prostate Cancer. ... In basal cells, normally a single-layer (left), nuclear enlargement can be found. The cells may become so hyperplastic that ... In basal cells, normally a single-layer (left), nuclear enlargement can be found. The cells may become so hyperplastic that ... Increased TP53 expression occurs after radiation, indicating that cells with abnormal overexpression were protected from cell ...
Human DEFα5 (Defensin Alpha 5, Paneth Cell Specific) ELISA Kit , G-EC-03282 ... Mouse DEFa5 (Defensin Alpha 5, Paneth Cell Specific) ELISA Kit , G-EC-04309 ... Rat SDF2L1 (Stromal Cell Derived Factor 2 Like Protein 1) ELISA Kit , G-EC-05665 Rat SDF2L1 (Stromal Cell Derived Factor 2 Like ... Rat SDF-1α (Stromal Cell Derived Factor 1α) ELISA Kit , G-EC-05922 Rat SDF-1α (Stromal Cell Derived Factor 1α) ELISA Kit , G-EC ...
... which is indicative of defects in Paneth cell differentiation. By contrast, development of Goblet cells, enteroendocrine cells ... A vesicle trafficking protein αSNAP regulates Paneth cell differentiation in vivo. Lechuga S, et al. Biochem Biophys Res Commun ... Title: A vesicle trafficking protein αSNAP regulates Paneth cell differentiation in vivo. ... mice harbor significant defects in CD4 T cell gene expression and Foxp3 regulatory T cell (Treg) differentiation. Title: Na(+) ...
Showing cell type specific RNA data of SEMA3B (LUCA-1, SemA, sema5, SEMAA, semaV). ... Intestinal goblet cells. c-2. Undifferentiated cells. c-3. Paneth cells. c-4. Intestinal goblet cells. ... There are 2 options for color schemes: 1) cell type color, which is based on cell type groups used in the Single Cell Type ... UMAP PLOT visualizes the cells in each cluster; where each dot corresponds to a cell. For each individual cell, mouseover ...
Categories: Paneth Cells Image Types: Photo, Illustrations, Video, Color, Black&White, PublicDomain, CopyrightRestricted 1 ...
Autophagy-Mediated Innate Defense Mechanism in Crypt Paneth Cells Responding To Impairment of Small Intestine Barrier after ...
Paneth cells produce and secrete antimicrobial products that protect the mucosa from pathogens. Their loss is associated with ... Parenteral Nutrition Decreases Paneth Cell Function and Intestinal Bactericidal Activity While Increasing Susceptibility to ... Interactions between dendritic cells (DCs) and environmental, dietary and pathogen antigens play a key role in immune ... The Effect of Cranberry Proanthocyanidins on Gut Barrier Function and Inflammation in an In Vitro Cell Co-Culture Model ...
Paneth cells as the cornerstones of intestinal and organismal health : a primer Charlotte Wallaeys (UGent) , Natalia Garcia ... Circulating and endometrial cell oxidative stress in dairy cows diagnosed with metritis Sanjana Malledevarahalli Chandrappa, ... Commensal bacteria of the lung microbiota synergistically inhibit inflammation in a three-dimensional epithelial cell model ... gamma t inhibition ameliorates IL-23 driven experimental psoriatic arthritis by predominantly modulating gamma delta-T cells ...
Paneth cells as the cornerstones of intestinal and organismal health : a primer Charlotte Wallaeys (UGent) , Natalia Garcia ... Inhibition of transcription by dactinomycin reveals a new characteristic of immunogenic cell stress Juliette Humeau, Allan ...
Human intelectin-2 (ITLN2) is selectively expressed by secretory Paneth cells E. B. Nonnecke, P. A. Castillo, Malin E V ... cells. Martin Lidell, Malin E V Johansson, Matthias Mörgelin, Noomi Asker, James R Gum, Young S Kim, Gunnar C. Hansson The ... cells Sinan Sharba, Nazanin Navabi, Médea Padra, Macarena P Quintana-Hayashi, Jenny K Gustafsson, Louis Szeponik, Vignes ... New developments in goblet cell mucus secretion and function George M. H. Birchenough, Malin E V Johansson, Jenny K Gustafsson ...
... chemoresistance and recurrence is the result of a small population of cancer cells with self-renewal and pluripotency ... involved in the regenerative process of the normal intestine and the identity of putative somatic intestinal stem cells have ... the paneth cell and the acidophilic plasma cell. Arch. Pathol. 1948, 46, 107-118. [Google Scholar] ... Colon cancer stem cells dictate tumor growth and resist cell death by production of interleukin-4. Cell Stem Cell 2007, 1, 389- ...
The small amount of goblet cells was seen but Paneths cells were not detected. The tumor had a large proportion of mitotic ... Immunohistochemical feature of the tumor cells. (a, b) Almost all tumor cells are positive for (a) CK20, but the cells are ... The cells were columnar with ovoid nuclei, often stratified and sometimes proliferating into gland-in-gland pattern. The cells ... c) Tumor cells show high-grade nuclear atypia. (d) PAS staining shows positive staining for the goblet cells. ...

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