Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P10721 (c-kit)
 6,575 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The interstitial cells of Cajal (ICC) are c-kit immunoreactive cells of the gastrointestinal tract which are suggested to have a role in the control of intestinal motility. Cells with c-kit immunoreactivity have not been previously described in the gastrointestinal tract of the horse. Immunoreactivity for c-kit was revealed using immunohistochemical labelling with an anti-c-kit polyclonal antibody. Sections of normal gastrointestinal tissue were examined from 13 anatomically defined sites from stomach to small colon taken from horses free from gastrointestinal disease. Three types of c-kit immunoreactive cells were identified: spindle-shaped cells in the region of the myenteric plexus, stellate or bipolar cells in the circular muscle layer, and round cells in the submucosa. The round cells were shown to be mast cells with the use of toluidine blue staining, whereas the other c-kit immunoreactive cells did not exhibit metachromasia and were classified as ICC. This study will serve as a basis for future pathological studies in the horse.
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PMID:An immunohistochemical study of interstitial cells of Cajal (ICC) in the equine gastrointestinal tract. 1033 70

Equine dysautonomia (grass sickness) is a common, frequently fatal disease of horses characterised by dysfunction of the gastrointestinal tract. Interstitial cells of Cajal are the c-Kit-immunoreactive cells responsible for the generation of pacemaker activity in gastrointestinal smooth muscle. Impairment of this pacemaker action has been implicated in several motility disorders in humans and laboratory mammals. The aim of this study was to test the hypothesis that changes in interstitial cells of Cajal may be involved in the pathophysiology of the intestinal dysfunction observed in equine grass sickness. Interstitial cells of Cajal were identified using immunohistochemical labelling with an anti-c-Kit antibody and their density was assessed using a semi-quantitative grading system. Segments of ileum were examined from 24 horses free from gastrointestinal disease and compared to tissues from 28 horses with grass sickness. Segments of the pelvic flexure region of the large colon were examined from 13 horses free from gastrointestinal disease and compared to tissues from 10 horses with grass sickness. In horses with grass sickness, interstitial cells of Cajal were significantly decreased in both the myenteric plexus and circular muscle regions of both ileum and pelvic flexure compared to normal animals. Therefore, it is possible that the decline in interstitial cells of Cajal may be an important factor in the development of intestinal dysmotility observed in grass sickness.
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PMID:A reduction in interstitial cells of Cajal in horses with equine dysautonomia (grass sickness). 1157 Jul 2

Equine dysautonomia (grass sickness) is a frequently fatal disease of horses characterised by intestinal stasis. Interstitial cells of Cajal (ICC) are the pacemakers and mediators of neurotransmission in the gastrointestinal tract. Impaired ICC-mediated control of motility has been implicated in intestinal disorders in laboratory mammals, humans and in equine grass sickness. The aim of this study was to compare the in vitro electrical properties of ileum from grass sickness cases with horses free from gastrointestinal disease. Intracellular microelectrode recordings were made from smooth muscle cells in cross-sectional preparations of equine ileum, superfused in vitro. Samples were taken from six horses with grass sickness and from eight horses free from gastrointestinal disease, all euthanised on humane grounds. Ileal tissues were processed for haematoxylin and eosin histology, and c-Kit immunohistochemistry. Membrane potential oscillations were recorded in the ileal preparations from four of the six horses with grass sickness and from all of the normal horses. A waxing and waning pattern of the membrane potential oscillation activity was noted in some cells. In comparison to the normal horses, the membrane potential oscillations in grass sickness horses had a significantly reduced frequency (P = 0.0001) and increased duration (P = 0.0002). Immunohistochemistry revealed the presence but reduction of ICC in grass sickness. Histological assessment of the same tissues used for analysis of the ICC showed the depletion and pathology of the enteric neurons in grass sickness. Therefore, the majority of ileal preparations from grass sickness-affected horses exhibited prominent membrane potential oscillation activity suggesting that, although the neural elements are damaged severely, the ICC-mediated pacemaker function remains intact.
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PMID:Presence of in vitro electrical activity in the ileum of horses with enteric nervous system pathology: equine dysautonomia (grass sickness). 1224 Oct 86

Damage to interstitial cells of Cajal (ICC), pacemakers, and mediators of neuromuscular neurotransmission in the gastrointestinal tract contributes to the pathogenesis of diabetic gastroenteropathy in both patients and animal models. ICC depletion in diabetes may result from chronic hyperglycemia or lost/ineffective insulin signaling. Because independent control of insulin and glucose concentrations is difficult in chronic in vivo studies, we used long-term organotypic cultures to address this problem. Murine gastric muscles were cultured in normoglycemic or hyperglycemic basal media with or without insulin or IGF-I for 1-3 months, the time required for gastroparesis and ICC damage to develop in diabetic mice. ICC were assessed by c-Kit immunohistochemistry and quantitative analysis of c-kit expression. Electrical pacemaking was studied by intracellular recording of slow waves. ICC survived for at least 34 days in unsupplemented normoglycemic media, but their networks, c-kit expression, and slow waves were profoundly reduced after 68 days. These changes could be entirely prevented by insulin or IGF-I supplementation. ICC networks were completely resistant to hyperglycemia for at least 72 days. Thus, hyperglycemia is unlikely to be responsible for the diabetes-associated depletion of ICC. In contrast, maintenance of ICC requires insulin or IGF-I, which are reduced or ineffective in diabetes.
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PMID:Reduced insulin and IGF-I signaling, not hyperglycemia, underlies the diabetes-associated depletion of interstitial cells of Cajal in the murine stomach. 1585 42