Dll4-selective Notch signaling induces ephrinB2 gene expression in endothelial cells

被引:73
作者
Iso, T
Maeno, T
Oike, Y
Yamazaki, M
Doi, H
Arai, M
Kurabayashi, M
机构
[1] Gunma Univ, Grad Sch Med, Dept Med & Biol Sci, Maebashi, Gumma 3718511, Japan
[2] Keio Univ, Sch Med, Sakaguchi Lab, Dept Cell Differentiat,Shinjuku Ku, Tokyo 1608582, Japan
关键词
arterial-venous differentiation; endothelial cells; Notch signaling; Jagged1; Dll4; HERP; EphrinB2; EphB4; TGF-beta; ALK1;
D O I
10.1016/j.bbrc.2006.01.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Notch pathway is involved in multiple aspects of vascular development, including arterial-venous differentiation. Here, we show that Notch stimulation instructively induces arterial characteristics in endothelial cells (EC). Forced expression of Notch intracellular domain (NICD, activated form of Notch) induced mRNA expression for a subset of arterial-specific markers such as ephrinB2, connexin40, and HERP1 only in EC but not other cell lines. In co-culture experiments using EC and either DII4- or Jagged1-expressing cells, we found that DIN stimulation but not Jagged1 markedly induced ephrinB2 expression. An inducible expression of HERP1 and HERP2 by NICD has no measurable effects on expression of ephrinB2 and venous marker EphB4 although either HERP1 or HERP2 overexpression exerts potent inhibitory effects on EphB4 expression without ephrinB2 induction. We also found no functional interaction between Notch and TGF-beta-ALK1 signalings in an induction of ephrinB2 expression. These results suggest that DII4-stimulated Notch signaling induces a part of arterial characteristics only in EC via HERP-independent mechanism. Our data provide new insight into the molecular mechanism of ligand-selective Notch activation during differentiation of arterial EC. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:708 / 714
页数:7
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