Differentiation of arterial and venous endothelial cells and vascular morphogenesis

被引:35
|
作者
Hirashima, Masanori [1 ]
Suda, Toshio [1 ]
机构
[1] Keio Univ, Sch Med, Sakaguchi Lab Dev Biol, Shinjuku Ku, Tokyo 1608582, Japan
来源
关键词
artery; endothelial cells; mouse; notch; vascular morphogenesis; VEGF; vein; zebrafish;
D O I
10.1080/10623320600698078
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The vascular system is comprised of an organized hierarchical structure of arteries, veins, and capillaries. Recent studies in zebrafish, chick, and mouse reveal that the identity of artery and vein is governed by genetic factors as well as blood flow. The ephrin/Eph system establishes arterial and venous endothelial cell identity, and is important for structural segregation between arteries and veins. Analyses using loss- or gain-of-function mutations in zebrafish and mice show that Su(H)/RBP-J-dependent Delta/Notch signaling is a key mediator of arterial endothelial cell fate decision and vascular patterning. Vascular endothelial growth factor has also been shown to work upstream of Notch and is a key player in arteriogenesis. On the other hand, an orphan nuclear receptor, COUP-TFII, induces venous endothelial cell differentiation by suppressing the Notch signaling. Arteriovenous malformations are frequently induced by a loss of arterial and venous cell specification. These insights indicate that the balance of these genetic factors and modification by epigenetic factors such as hemodynamics and oxygen tension are important for proper endothelial cell identities in vascular morphogenesis.
引用
收藏
页码:137 / 145
页数:9
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