Senescence mechanisms and targets in the heart

被引:148
作者
Chen, Maggie S. [1 ,2 ]
Lee, Richard T. [1 ,2 ,3 ,4 ]
Garbern, Jessica C. [1 ,2 ,5 ]
机构
[1] Harvard Univ, Dept Stem Cell & Regenerat Biol, 7 Divin Ave, Cambridge, MA 02138 USA
[2] Harvard Univ, Harvard Stem Cell Inst, 7 Divin Ave, Cambridge, MA 02138 USA
[3] Brigham & Womens Hosp, Dept Med, Div Cardiovasc Med, 75 Francis St, Boston, MA 02115 USA
[4] Harvard Med Sch, 75 Francis St, Boston, MA 02115 USA
[5] Boston Childrens Hosp, Dept Cardiol, 300 Longwood Ave, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
Senescence; Ageing; Cardiovascular disease; Senotherapy; MUSCLE-CELL SENESCENCE; DNA-DAMAGE RESPONSE; SECRETORY PHENOTYPE; HUMAN ATHEROSCLEROSIS; PREMATURE SENESCENCE; PRECISION MEDICINE; SENOLYTIC AGENT; EMERGING ROLE; TELOMERE; EXPRESSION;
D O I
10.1093/cvr/cvab161
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cellular senescence is a state of irreversible cell cycle arrest associated with ageing. Senescence of different cardiac cell types can direct the pathophysiology of cardiovascular diseases (CVDs) such as atherosclerosis, myocardial infarction, and cardiac fibrosis. While age-related telomere shortening represents a major cause of replicative senescence, the senescent state can also be induced by oxidative stress, metabolic dysfunction, and epigenetic regulation, among other stressors. It is critical that we understand the molecular pathways that lead to cellular senescence and the consequences of cellular senescence in order to develop new therapeutic approaches to treat CVD. In this review, we discuss molecular mechanisms of cellular senescence, explore how cellular senescence of different cardiac cell types (including cardiomyocytes, cardiac endothelial cells, cardiac fibroblasts, vascular smooth muscle cells, and valve interstitial cells) can lead to CVD, and highlight potential therapeutic approaches that target molecular mechanisms of cellular senescence to prevent or treat CVD.
引用
收藏
页码:1173 / 1187
页数:15
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