Angiopoietin-1 inhibits endothelial cell apoptosis via the Akt/survivin pathway

被引:496
作者
Papapetropoulos, A
Fulton, D
Mahboubi, K
Kalb, RG
O'Connor, DS
Li, FZ
Altieri, DC
Sessa, WC
机构
[1] Yale Univ, Sch Med, Boyer Ctr Mol Med 436D, Dept Pharmacol, New Haven, CT 06536 USA
[2] Yale Univ, Sch Med, Boyer Ctr Mol Med, Dept Pathol, New Haven, CT 06536 USA
[3] Yale Univ, Sch Med, Boyer Ctr Mol Med, Dept Neurol, New Haven, CT 06536 USA
关键词
D O I
10.1074/jbc.275.13.9102
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
A productive angiogenic response must couple to the survival machinery of endothelial cells to preserve the integrity of newly formed vessels. Angiopoietin-1 (Ang-l) is an endothelium-specific ligand essential for embryonic vascular stabilization, branching morphogenesis, and post-natal angiogenesis, but its contribution to endothelial cell survival has not been completely elucidated. Here we show that Ang-l acting via the Tie 2 receptor induces phosphorylation of the survival serine-threonine kinase, Akt (or protein kinase B). This is associated with up-regulation of the apoptosis inhibitor, survivin, in endothelial cells and protection of endothelium from death-inducing stimuli. Moreover, dominant negative survivin negates the ability of Ang-l to protect cells from undergoing apoptosis, The activation of antiapoptotic pathways mediated by Akt and survivin in endothelial cells may contribute to Ang-l stabilization of vascular structures during angiogenesis, in vivo.
引用
收藏
页码:9102 / 9105
页数:4
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