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SIRT3表观遗传学和心力衰竭病理变化的研究进展

Progress in SIRT3 Epigenetics and Pathological Changes in Heart Failure
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摘要 心力衰竭是各种心脏疾病的终末阶段,其病理过程贯穿发病的各个环节。SIRT3是SIRTUIN家族的重要一员,属于烟酰胺腺嘌呤二核苷酸(NAD+)依赖性脱乙酰酶的Sirtuin家族,亚细胞主要定位于线粒体,在心脏中高度表达。表观遗传学不牵涉DNA的序列变化,而基因组相关功能改变,比如组蛋乙酰化相关的SIRT3可通过各种通路及调节因子,对心肌纤维化、心肌肥厚、心肌凋亡等病理过程进行调节,对心力衰竭的发生、发展产生重要影响。本文主要综述SIRT3在心力衰竭各病理过程中的研究进展。Heart failure is the terminal stage of various heart diseases, and its pathological process runs through every link of the disease. SIRT3 is an important member of the Sirtuin family, belonging to the sirtuin family of nicotinamide adenine dinucleotide (NAD+)-dependent deacetylases, which is subcellular localized in mitochondria and is highly expressed in the heart. Epigenetics does not involve the sequence changes of DNA, but genome-related functional changes, such as egg acetylation- related SIRT3, can regulate myocardial fibrosis, myocardial hypertrophy, myocardial apoptosis and other pathological processes through various pathways and regulatory factors, and have an important impact on the occurrence and development of heart failure. This paper mainly reviews the progress of SIRT3 in each pathological process of heart failure.
出处 《医学诊断》 2024年第3期256-264,共9页 Medical Diagnosis
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  • 1无.慢性心力衰竭诊断治疗指南[J].中华心血管病杂志,2007,35(12):1076-1095. 被引量:3684
  • 2Lewis BP, Burge CB, Barrel DP. Conserved seed pairing, often flanked by adeno- sines,indicates that thousands of human genes are microRNA targets[ J ]. Cell, 2005,120 : 15-20.
  • 3Grey F, Tirabassi R, Meyers H,et al. A viral microRNA down-regulates multiple cell cycle genes through mRNA 5'UTRs [ J ]. PLoS Pathog, 2010, 6 (6) : e1000967.
  • 4Ono K,Kuwabara Y,Han J. Mof NAs and cardiovascular diseases[ J ]. FEBS J,2011,278(10) :1619-1633.
  • 5Chen CZ. An unsolved mystery: the target-recognizlng RNA species of microRNA genes [ J ]. Biochimie,2013,95 ( 9 ) : 1663 -1676.
  • 6Liu N, Bezprozvannaya S,Williams AH,et al, MicroRNA-133a regulates cardio- myocyte prtliferation and suppresses smooth muscle geue expression in the heart [ J ]. Genes Dev, 2008,22 ( 23 ) : 3242-3254.
  • 7Schneider M, Andeen DC, Silahtaroglu A, et al. Cell-specific detection of mi- croRNA expression during cardiomyogenesis by combined in situ hybridization and i mmunohistochemistry [ J ]. J Mol Histo1,2011,42 (4) : 289-299.
  • 8van Rooij E, Marshall WS, Olson EN. Toward miemRNA based therapeutics for h eart disease : the sense in antisense [ J ]. Circ Res, 2008,103 ( 9 ) : 919 -928.
  • 9Thum T,Gross C, Fiedler J, et al. MiroRNA-21 contributes to myocardial dis- ease by stimulating MAP kinase signalling in fibroblasts [ J ]. Nature,2008,456 (7224) :980-984.
  • 10Ivey KN, Mutb A, Arnold J.et al. MieroRNA regulalion of cell lineages in mouse and human embryonic: stem cells [ J ]. Cell Stem Ce11,2008,2 ( 3 ) :219 -229.

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