期刊
HUMAN MOLECULAR GENETICS
卷 12, 期 24, 页码 3307-3314出版社
OXFORD UNIV PRESS
DOI: 10.1093/hmg/ddg355
关键词
-
资金
- NIDDK NIH HHS [R01 DK021344] Funding Source: Medline
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.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据