Epigenetics, cardiovascular disease, and cellular reprogramming

被引:25
作者
Al-Hasani, Keith [1 ]
Mathiyalagan, Prabhu [2 ]
El-Osta, Assam [1 ,3 ]
机构
[1] Monash Univ, Dept Diabet, Epigenet Human Hlth & Dis Lab, Melbourne, Vic, Australia
[2] Icahn Sch Med Mt Sinai, Cardiovasc Res Ctr, New York, NY 10029 USA
[3] Chinese Univ Hong Kong, Prince Wales Hosp, Hong Kong Inst Diabet & Obes, Hong Kong, Peoples R China
基金
中国国家自然科学基金; 英国医学研究理事会;
关键词
GENE-EXPRESSION; CARDIAC-HYPERTROPHY; HISTONE DEACETYLATION; STEM-CELLS; INHIBITION; MICRORNA; DIFFERENTIATION; PROMOTES; METHYLATION; FIBROBLASTS;
D O I
10.1016/j.yjmcc.2019.01.019
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Under the seeming disorder of "junk" sequences the last decade has seen developments in our understanding of non-coding RNA's (ncRNAs). Its a complex revised order and nowhere is this more relevant than in the developing heart whereby old rules have been set aside to make room for new ones. The development of the mammalian heart has been studied at the genetic and cellular level for several decades because these areas were considered ideal control points. As such, detailed mechanisms governing cell lineages are well described. Emerging evidence suggests a complex new order regulated by epigenetic mechanisms mark cardiac cell lineage. Indeed, molecular cardiologists are in the process of shedding light on the roles played by ncRNAs, nucleic acid methylation and histone/chromatin modifications in specific pathologies of the heart. The aim of this article is to discuss some of the recent advances in the field of cardiovascular epigenetics that are related to direct cell reprogramming and repair. As such, we explore ncRNAs as nodes regulating signaling networks and attempt to make sense of regulatory disorder by reinforcing the importance of epigenetic components in the developmental program.
引用
收藏
页码:129 / 133
页数:5
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