Hnf6 and Tcf2 (MODY5) are linked in a gene network operating in a precursor cell domain of the embryonic pancreas

被引:116
作者
Maestro, MA
Boj, SF
Luco, RF
Pierreux, CE
Cabedo, J
Servitja, JM
German, MS
Rousseau, GG
Lemaigre, FP
Ferrer, J
机构
[1] Hosp Clin Barcelona, Inst Invest Biomed August Pi & Sunyer, Barcelona, Spain
[2] Univ Calif San Francisco, Hormone Res Inst, San Francisco, CA 94143 USA
[3] Catholic Univ Louvain, Hormone & Metab Res Unit, B-1200 Brussels, Belgium
[4] Inst Cellular Pathol, Brussels, Belgium
关键词
D O I
10.1093/hmg/ddg355
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During pancreatic organogenesis endocrine cells arise from non self-renewing progenitors that express Ngn3. The precursors that give rise to Ngn3(+) cells are presumably located within duct-like structures. However, the nature of such precursors is poorly understood. We show that, at E13-E18, the embryonic stage during which the major burst of beta-cell neogenesis takes place, pancreatic duct cells express Hnf1beta, the product of the maturity-onset diabetes of the young type 5 (MODY5) gene. Ngn3(+) cells at this stage invariably cluster with mitotically competent Hnf1beta(+) cells, and are often intercalated with these cells in the epithelium that lines the lumen of primitive ducts. We present several observations that collectively indicate that Hnf1beta(+) cells are the immediate precursors of Ngn3(+) cells. We furthermore show that Hnf1beta expression is markedly reduced in early pancreatic epithelial cells of Hnf6-deficient mice, in which formation of Ngn3(+) cells is defective. These findings define a precursor cellular stage of the embryonic pancreas and place Hnf1beta in a genetic hierarchy that regulates the generation of pancreatic endocrine cells.
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页码:3307 / 3314
页数:8
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