Notch4 and Jagged-1 induce microvessel differentiation of rat brain endothelial cells

被引:58
作者
Uyttendaele, H
Closson, V
Wu, GY
Roux, F
Weinmaster, G
Kitajewski, J
机构
[1] Columbia Univ Coll Phys & Surg, Dept Pathol & OB GYN, New York, NY 10032 USA
[2] Hop Fernand Widal, INSERM, U26, F-75010 Paris, France
[3] Univ Calif Los Angeles, Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USA
关键词
Notch4; Jagged-1; endothelial; microvessels; morphogenesis;
D O I
10.1006/mvre.2000.2254
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The mouse Notch4 gene is expressed specifically in endothelial cells. Notch4/int-3, a truncated form of Notch4, acts as a constitutive activated Notch receptor. We used rat brain microvessel endothelial cells (RBE4) to study the role of Notch4 and Jagged-1 in endothelial cell differentiation. Both Notch4/int-3 and Jagged-1 were able to induce microvessel-like structures with morphological and biochemical properties similar to brain endothelial microvessels. Ectopic expression of full-length Notch4 did not effect RBE4 cells. Activation of the Notch signal transduction pathway was measured by the induction of endogenous Notch4 and Jagged-1 genes and of Jagged-1 proteins. The observed morphological changes to RBE4 cells correlated with endogenous Notch4 and Jagged-1 gene activation. Our observations demonstrate that Notch signaling can promote endothelial cell differentiation and morphogenesis. (C) 2000 Academic Press.
引用
收藏
页码:91 / 103
页数:13
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