生物
血管生成
循环系统
Notch信号通路
胚胎干细胞
血管
细胞命运测定
背主动脉
血管生成
祖细胞
细胞生物学
解剖
转录因子
信号转导
内分泌学
遗传学
干细胞
基因
作者
Matthew Swift,Brant M. Weinstein
出处
期刊:Circulation Research
[Lippincott Williams & Wilkins]
日期:2009-03-12
卷期号:104 (5): 576-588
被引量:409
标识
DOI:10.1161/circresaha.108.188805
摘要
The major arteries and veins of the vertebrate circulatory system are formed early in embryonic development, before the onset of circulation, following de novo aggregation of “angioblast” progenitors in a process called vasculogenesis. Initial embryonic determination of artery or vein identity is regulated by variety of genetic factors that work in concert to specify endothelial cell fate, giving rise to 2 distinct components of the circulatory loop possessing unique structural characteristics. Work in multiple in vivo animal model systems has led to a detailed examination of the interacting partners that determine arterial and venous specification. We discuss the hierarchical arrangement of many signaling molecules, including Hedgehog (Hh), vascular endothelial growth factor (VEGF), Notch, and chicken ovalbumin upstream-transcription factor II (COUP-TFII) that promote or inhibit divergent pathways of endothelial cell fate. Elucidation of the functional role of these genetic determinants of blood vessel specification together with the epigenetic factors involved in subsequent modification of arterial–venous identity will allow for potential new therapeutic targets for vascular disorders.
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