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

Citation
Jm. Vanderwinden et al., CD34 immunoreactivity and interstitial cells of Cajal in the human and mouse gastrointestinal tract, CELL TIS RE, 302(2), 2000, pp. 145-153
Citations number
25
Categorie Soggetti
Cell & Developmental Biology
Journal title
CELL AND TISSUE RESEARCH
ISSN journal
0302766X → ACNP
Volume
302
Issue
2
Year of publication
2000
Pages
145 - 153
Database
ISI
SICI code
0302-766X(200011)302:2<145:CIAICO>2.0.ZU;2-G
Abstract
Immunoreactivity for the tyrosine kinase receptor Kit (Kit-ir) is an establ ished 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 expr essing both CD34-ir and Kit-ir remains controversial. CD34-ir and Kit-ir we re studied by high-resolution confocal microscopy on cryostat sections of h uman and murine gut as well as murine whole-mounts, using specific antibodi es 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 consistentl y 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 meso thelial cells. CD34-ir is not a marker for Kit-ir ICC in the human and muri ne gut. No CD34-ir, Kit-ir-expressing cells were encountered. Conversely, C D34-ir cells, closely adjacent to, but distinct from, Kit-ir ICC were consi stently identified. The intimate relationship between these cells may offer an alternative explanation for reports of CD34 and Kit co-localization. Th e ontogeny and function of CD34-ir cells in the gut, as well as the origin of gastrointestinal stromal tumors, remain unclear.