MicroRNA-34a regulates cardiac ageing and function

被引:676
作者
Boon, Reinier A. [1 ]
Iekushi, Kazuma [1 ]
Lechner, Stefanie [2 ]
Seeger, Timon [1 ,3 ]
Fischer, Ariane [1 ]
Heydt, Susanne [1 ]
Kaluza, David [1 ]
Treguer, Karine [1 ]
Carmona, Guillaume [1 ]
Bonauer, Angelika [1 ]
Horrevoets, Anton J. G. [4 ]
Didier, Nathalie [5 ]
Girmatsion, Zenawit [3 ]
Biliczki, Peter [3 ]
Ehrlich, Joachim R. [3 ]
Katus, Hugo A. [6 ,7 ]
Mueller, Oliver J. [6 ,7 ]
Potente, Michael [1 ,3 ]
Zeiher, Andreas M. [3 ,7 ]
Hermeking, Heiko [2 ]
Dimmeler, Stefanie [1 ,7 ]
机构
[1] Goethe Univ Frankfurt, Ctr Mol Med, Inst Cardiovasc Regenerat, D-60590 Frankfurt, Germany
[2] Univ Munich, Inst Pathol, D-80337 Munich, Germany
[3] Goethe Univ Frankfurt, Dept Cardiol, D-60590 Frankfurt, Germany
[4] Vrije Univ Amsterdam Med Ctr, Dept Mol Cell Biol & Immunol, NL-1081 BT Amsterdam, Netherlands
[5] Univ Paris 06, INSERM, Myol Grp, Inst Myol,UMR S787, Paris, France
[6] Univ Heidelberg Hosp, D-69120 Heidelberg, Germany
[7] German Ctr Cardiovasc Res DZHK, D-13347 Berlin, Germany
基金
欧洲研究理事会;
关键词
MYOCARDIAL-INFARCTION; HEART FUNCTION; APOPTOSIS; P53; ANGIOGENESIS; PHOSPHATASE; ACTIVATION; SENESCENCE; EXPRESSION; COMPONENT;
D O I
10.1038/nature11919
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ageing is the predominant risk factor for cardiovascular diseases(1) and contributes to a significantly worse outcome in patients with acute myocardial infarction(2). MicroRNAs (miRNAs) have emerged as crucial regulators of cardiovascular function and some miRNAs have key roles in ageing(3,4). We propose that altered expression of miRNAs in the heart during ageing contributes to the age-dependent decline in cardiac function. Here we show that miR-34a is induced in the ageing heart and that in vivo silencing or genetic deletion of miR-34a reduces age-associated cardiomyocyte cell death. Moreover, miR-34a inhibition reduces cell death and fibrosis following acute myocardial infarction and improves recovery of myocardial function. Mechanistically, we identified PNUTS (also known as PPP1R10) as a novel direct miR-34a target, which reduces telomere shortening, DNA damage responses and cardiomyocyte apoptosis, and improves functional recovery after acute myocardial infarction. Together, these results identify age-induced expression of miR-34a and inhibition of its target PNUTS as a key mechanism that regulates cardiac contractile function during ageing and after acute myocardial infarction, by inducing DNA damage responses and telomere attrition.
引用
收藏
页码:107 / 110
页数:4
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