Expression of Active Notch1 in Avian Coronary Development

被引:19
|
作者
Yang, Ke [1 ]
Doughman, Yong-Qiu [1 ]
Karunamuni, Ganga [1 ]
Gu, Shi [2 ]
Yang, Yu-Chung [2 ]
Bader, David M. [3 ]
Watanabe, Michiko [1 ]
机构
[1] Case Western Reserve Univ, Sch Med, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Sch Med, Dept Biochem, Cleveland, OH 44106 USA
[3] Vanderbilt Univ, Med Ctr, Nashville, TN USA
关键词
chicken embryo; heart development; coronary development; Notch1ICD; pro-epicardial organ; epicardium-derived cells; ENDOTHELIAL-GROWTH-FACTOR; EPICARDIUM-DERIVED CELLS; MESENCHYMAL TRANSITION; MYOCARDIAL HYPOXIA; LATERAL INHIBITION; INNER-EAR; HEART; DIFFERENTIATION; VASCULOGENESIS; POPULATION;
D O I
10.1002/dvdy.21811
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
100101 ;
摘要
Notch1 is an important regulator of intercellular interactions in cardiovascular development. We show that the nuclear-localized, cleaved and active form of Notch1, the Notch1 intracellular domain (N1ICD), appeared in mesothelial cells of the pro-epicardium during epicardial formation at looped heart stages. N1ICD was also present in mesothelial cells and mesenchymal cells specifically within the epicardium at sulcus regions. N1ICD-positive endothelial cells were detected within the nascent vessel plexus at the atrioventricular junction and within the compact myocardium (Hamburger and Hamilton stage [HH] 25-HH30). The endothelial cells expressing N1ICD were surrounded by N1ICD-positive smooth muscle cells after coronary orifice formation (HH32-HH35), while N1ICD expression was absent in the mesenchymal and mesothelial cells surrounding mature coronary vessels. We propose that differential activation of the hypoxia/HIF1-VEGF-Notch pathway may play a role in epicardial cell interactions that promote epicardial epithelial/mesenchymal transition and coronary progenitor cell differentiation during epicardial development and coronary vasculogenesis in particularly hypoxic sulcus regions. Developmental Dynamics 238:162-170, 2009. (C) 2008 Wiley-Liss, Inc.
引用
收藏
页码:162 / 170
页数:9
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