Neurogenin3 Initiates Stepwise Delamination of Differentiating Endocrine Cells During Pancreas Development

被引:119
作者
Gouzi, Mathieu [1 ]
Kim, Yung Hae [1 ]
Katsumoto, Keiichi [1 ]
Johansson, Kerstin [1 ]
Grapin-Botton, Anne [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Sch Life Sci, Swiss Inst Expt Canc Res, CH-1015 Lausanne, Switzerland
关键词
beta cells; insulin; snail; endoderm; islet; Langerhans; delamination; EPITHELIAL-MESENCHYMAL TRANSITION; TRANSCRIPTION FACTORS; E-CADHERIN; INSULIN-SECRETION; PROGENITOR CELLS; IN-VIVO; EXPRESSION; SNAIL; MIGRATION; MOUSE;
D O I
10.1002/dvdy.22544
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100123 [人体微生态学]; 100210 [外科学];
摘要
During development, pancreatic endocrine cells are specified within the pancreatic epithelium. They subsequently delaminate out of the epithelium and cluster in the mesenchyme to form the islets of Langerhans. Neurogenin3 (Ngn3) is a transcription factor required for the differentiation of all endocrine cells and we investigated its role in their delamination. We observed in the mouse pancreas that most Ngn3-positive cells have lost contact with the lumen of the epithelium, showing that the delamination from the progenitor layer is initiated in endocrine progenitors. Subsequently, in both mouse and chick newly born endocrine cells at the periphery of the epithelium strongly decrease E-cadherin, break-down the basal lamina and cluster into islets of Langerhans. Repression of E-cadherin is sufficient to promote delamination from the epithelium. We further demonstrate that Ngn3 indirectly controls Snail2 protein expression post-transcriptionally to repress E-cadherin. In the chick embryo, Ngn3 independently controls epithelium delamination and differentiation programs. Developmental Dynamics 240:589-604, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:589 / 604
页数:16
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