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Am J Physiol Endocrinol Metab 293: E475-E483, 2007. First published May 22, 2007; doi:10.1152/ajpendo.00172.2007
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Expression of c-Kit receptor tyrosine kinase and effect on beta-cell development in the human fetal pancreas

Jinming Li,1 Jaclyn Quirt,1 Hung Quoc Do,1 Kristina Lyte,1 Fraser Fellows,3 Cynthia G. Goodyer,4 and Rennian Wang1,2

Departments of 1Physiology and Pharmacology, 2Medicine, and 3Obstetrics and Gynecology, University of Western Ontario, London, Ontario; and 4Department of Pediatrics, McGill University, Montreal, Quebec, Canada

Submitted 16 March 2007 ; accepted in final form 22 May 2007

The receptor, c-Kit, and its ligand, stem cell factor (SCF), are critical for hematopoietic stem cell differentiation and have been implicated in the development, function, and survival of rodent islets. Previously, we reported that exogenous SCF treatments of cultured human fetal (14–16 wk fetal age) islet-epithelial clusters enhanced islet cell differentiation and proliferation (Li J, Goodyer CG, Fellows F, Wang R. Int J Biochem Cell Biol 38: 961–972, 2006). In the present study, we examined the expression pattern of c-Kit in early to midgestation human fetal pancreata and the relevance of c-Kit receptor tyrosine kinase for insulin gene expression and beta-cell survival. c-Kit is expressed in the intact pancreas in a cell-specific manner, with a significant decrease in immunoreactivity in the duct regions from 8 to 21 wk fetal age, paralleled by a significant increase in expression within endocrine regions. These c-Kit-positive cells are highly proliferative and show frequent coexpression with insulin and glucagon. Treatment of islet-epithelial clusters with anti-ACK45 antibody stimulates c-Kit phosphorylation paralleled by a significant increase in PDX-1 and insulin expression, increased cell proliferation, and reduced beta-cell death. In contrast, transient transfection with c-Kit siRNA results in a three- to fourfold decrease in c-Kit, PDX-1, and insulin expression and decreased cell proliferation. This study describes important changes in the distribution and dynamics of c-Kit-expressing cells during human fetal pancreatic neogenesis, suggesting that c-Kit may be a marker for human pancreatic islet progenitor cells. Functional analysis of the c-Kit receptor tyrosine kinase provides evidence that phosphorylation of c-Kit receptor may be involved in mediating early beta-cell differentiation and survival.

islet-epithelial cluster; anti-c-Kit antibody; c-Kit small interfering ribonucleic acid



Address for reprint requests and other correspondence: R. Wang, Victoria Research Laboratories, Rm. A5-140, 800 Commissioners Road East, London, ON, N6C 2V5, Canada (e-mail: rwang{at}uwo.ca)




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