Prohibitin-1 maintains the angiogenic capacity of endothelial cells by regulating mitochondrial function and senescence

被引:166
|
作者
Schleicher, Michael [1 ,2 ]
Shepherd, Benjamin R. [3 ]
Suarez, Yajaira [1 ,2 ,3 ]
Fernandez-Hernando, Carlos [1 ,2 ]
Yu, Jun [1 ,2 ]
Pan, Yong [4 ,5 ]
Acevedo, Lisette M. [1 ,2 ]
Shadel, Gerald S. [4 ]
Sessa, William C. [1 ,2 ]
机构
[1] Yale Univ, Sch Med, Dept Pharmacol & Vasc Biol, New Haven, CT 06536 USA
[2] Yale Univ, Sch Med, Therapeut Program, New Haven, CT 06536 USA
[3] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06536 USA
[4] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06536 USA
[5] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06520 USA
来源
JOURNAL OF CELL BIOLOGY | 2008年 / 180卷 / 01期
关键词
D O I
10.1083/jcb.200706072
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Prohibitin 1 (PHB1) is a highly conserved protein that is mainly localized to the inner mitochondrial membrane and has been implicated in regulating mitochondrial function in yeast. Because mitochondria are emerging as an important regulator of vascular homeostasis, we examined PHB1 function in endothelial cells. PHB1 is highly expressed in the vascular system and knockdown of PHB1 in endothelial cells increases mitochondrial production of reactive oxygen species via inhibition of complex I, which results in cellular senescence. As a direct consequence, both Akt and Rac1 are hyper-activated, leading to cytoskeletal rearrangements and decreased endothelial cell motility, e. g., migration and tube formation. This is also reflected in an in vivo angiogenesis assay, where silencing of PHB1 blocks the formation of functional blood vessels. Collectively, our results provide evidence that PHB1 is important for mitochondrial function and prevents reactive oxygen species-induced senescence and thereby maintains the angiogenic capacity of endothelial cells.
引用
收藏
页码:101 / 112
页数:12
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