运动诱导生理性心肌肥厚的非编码RNA调节机制

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  • 上海大学 生命科学学院, 上海 200444
肖俊杰,教授,国家自然科学基金委优秀青年科学基金获得者。
上海大学生命科学学院副院长, 上海大学心血管研究所所长,心脏再生与衰老实验室主任. 代表性论文发表在Nat Commun,Cell Metab, Circulation, Annu Rev Genomics 等杂志. 担任 J Cardiovasc Transl Res 杂志副主编,BMC Med,Cell Transplant, J ThoracDisBiomed Environ Sci 杂志编委.担任上海大学学术委员会委员、中国康复医学会心血管专业委员会常务委员、中国生物物理学会代谢生物学分会理事、中国生理学会循环生理专业委员会委员、中国病理生理学会心血管专业委员会青年委员、国际心脏研究会 (ISHR) 中国分会青年委员、国际心脏研究会中国转化医学工作委员会委员、中国老年学会衰老与抗衰老科学委员会委员、上海市康复医学会心血管专业委员会委员、上海市生理学会理事、上海细胞生物学学会委员.目前正主持国家自然科学基金委优秀青年科学基金在内的 3 项国家自然基金项目、1 项上海市教委重大创新项目、1 项上海市科委国际合作项目,获得 2016 年度上海人才发展资金资助,是上海市青年岗位能手和宝钢优秀教师奖获得者. 主要研究领域:心力衰竭的综合干预和风险预警策略.

收稿日期: 2019-05-21

  网络出版日期: 2019-06-24

基金资助

国家自然科学基金资助项目(81722008);国家自然科学基金资助项目(91639101);国家自然科学基金资助项目(81570362);上海市教委科研创新计划自然科学重大资助项目(2017-01-07-00-09-E00042);上海市科委部分地方院校能力建设资助项目(17010500100);上海市国际科技合作基金资助项目(18410722200)

Non-coding RNAs in exercise-induced cardiac hypertrophy

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  • School of Life Sciences, Shanghai University, Shanghai 200444, China

Received date: 2019-05-21

  Online published: 2019-06-24

摘要

大量研究表明运动训练对心脏具有保护作用. 运动可诱导生理性心肌肥厚,对于心力衰竭具有保护作用. 心肌肥厚可分为生理性和病理性心肌肥厚,后者可导致心脏功能受损、心力衰竭以及高死亡率. 近几十年来,非编码 RNA 包括微小 RNA (microRNA, miRNAs)、长链非编码 RNA (long noncodingRNA, lncRNAs) 和环状 RNA (circularRNA, circRNAs) 等,引起了研究者的极大关注,非编码 RNA 的失调被证实与多种心血管疾病密切相关. 综述了心肌肥厚,尤其是生理性心肌肥厚中 miRNAs,lncRNAs 和 circRNAs 的特征、功能和分子机制.同向调控这些运动影响的非编码 RNA 可以防治心力衰竭.

本文引用格式

王天慧, 肖俊杰 . 运动诱导生理性心肌肥厚的非编码RNA调节机制[J]. 上海大学学报(自然科学版), 2019 , 25(3) : 425 -434 . DOI: 10.12066/j.issn.1007-2861.2140

Abstract

Increasing evidence supports the protective role of exercise training in preventing cardiovascular diseases. Exercise induces physiological cardiac growth, and thus protects the heart against pathological remodeling and heart failure. Cardiac hypertrophy falls into two types, namely, the physiological cardiac hypertrophy and the pathological cardiac hypertrophy, and the latter can result in impaired cardiac functioning, heart failure and is predictive of a higher incidence of death due to cardiovascular diseases. Non-coding RNAs (ncRNAs) including microRNAs (miRNAs), long non-coding RNAs (lncRNAs) and circular RNAs (circRNAs) have drawn significant attention over the last couple of decades, and their dysregulation is increasingly being linked to many cardiovascular diseases. In this paper, the profiling function, and molecular mechanism of miRNAs, lncRNAs, and circ- RNAs in cardiac hypertrophy, especially in physiological hypertrophy have been analyzed. Targeting these ncRNAs represents novel therapy for heart failure.

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