Mechanisms of endothelial senescence

被引:72
作者
Erusalimsky, Jorge D.
Skene, Chris
机构
[1] Univ Wales Inst, Cardiff Sch Hlth Sci, Cardiff CF5 2YB, S Glam, Wales
[2] UCL, Wolfson Inst Biomed Res, London WC1E 6BT, England
关键词
REGULATES TELOMERASE ACTIVITY; FIBROBLAST GROWTH FACTOR-2; OXIDATIVE STRESS; NITRIC-OXIDE; CELL SENESCENCE; IN-VIVO; VASCULAR ENDOTHELIUM; BETA-GALACTOSIDASE; ATHEROSCLEROSIS; AORTA;
D O I
10.1113/expphysiol.2008.043133
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
When endothelial cells from different vascular beds are grown in culture they show a limited capacity to divide, eventually entering into a permanent and phenotypically distinctive non-dividing state referred to as 'replicative senescence'. Replicative senescence is thought to result from progressive shortening of telomeric DNA and consequent telomere dysfunction. More recently, it has been realised that senescence can also be induced by a variety of insults, including those causing intracellular oxidative stress. In this report, we review evidence for the occurrence of endothelial cell senescence in vivo. We will also examine the causes, mechanisms and regulation of this process as they emerge from our studies in cell culture, focusing in particular on the roles of oxidative stress, telomerase, growth factors and nitric oxide.
引用
收藏
页码:299 / 304
页数:6
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