CD34 immunoreactivity and interstitial cells of Cajal in the human and mouse gastrointestinal tract

被引:0
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作者
Jean-Marie Vanderwinden
Jüri J. Rumessen
Marc-Henri De Laet
Jean-Jacques Vanderhaeghen
Serge N. Schiffmann
机构
[1] Laboratoire de Neurophysiologie,
[2] Faculté de Médecine,undefined
[3] Université Libre de Bruxelles,undefined
[4] Campus Erasme,undefined
[5] CP 601,undefined
[6] 808 route de Lennik,undefined
[7] 1070 Brussels,undefined
[8] Belgium,undefined
[9] Department of Gastroenterology 439 and Institute of Pathology,undefined
[10] Hvidovre Hospital,undefined
[11] Hvidovre,undefined
[12] Denmark,undefined
[13] Department of Pediatric Surgery,undefined
[14] Hôpital Universitaire des Enfants Reine Fabiola,undefined
[15] Université Libre de Bruxelles,undefined
[16] Brussels,undefined
[17] Belgium,undefined
来源
Cell and Tissue Research | 2000年 / 302卷
关键词
Immunohistochemistry Confocal microscopy Co-localization Fibroblast-like cells Stromal tumors Mouse (C57 BL/6) Human;
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摘要
Immunoreactivity for the tyrosine kinase receptor Kit (Kit-ir) is an established marker for the interstitial cells of Cajal (ICC) of the gut. Recently, the presence of CD34 immunoreactivity (CD34-ir) has been reported in Kit-ir ICC around the myenteric plexus in human small intestine. Conversely, we observed that CD34-ir labeled Kit-negative fibroblast-like cells, closely adjacent to, but distinct from, the Kit-ir ICC. The existence of cells expressing both CD34-ir and Kit-ir remains controversial. CD34-ir and Kit-ir were studied by high-resolution confocal microscopy on cryostat sections of human and murine gut as well as murine whole-mounts, using specific antibodies raised to human and murine CD34, respectively. CD34-ir labeled numerous cells in all parts of the gut, in man and in mouse. CD34-ir was consistently observed in Kit-negative cells, distinct from the closely adjacent Kit-ir ICC. Thin processes of both cell types intermingled extensively, often at the limit of resolution for light microscopy. CD34-ir was also observed in Kit-negative mesenchymal cells in the submucosa, in capillaries and in mesothelial cells. CD34-ir is not a marker for Kit-ir ICC in the human and murine gut. No CD34-ir, Kit-ir-expressing cells were encountered. Conversely, CD34-ir cells, closely adjacent to, but distinct from, Kit-ir ICC were consistently identified. The intimate relationship between these cells may offer an alternative explanation for reports of CD34 and Kit co-localization. The ontogeny and function of CD34-ir cells in the gut, as well as the origin of gastrointestinal stromal tumors, remain unclear
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页码:145 / 153
页数:8
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