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组蛋白乙酰化位点在心肌肥厚和心力衰竭中的作用。

Roles of histone acetylation sites in cardiac hypertrophy and heart failure.

作者信息

Funamoto Masafumi, Imanishi Masaki, Tsuchiya Koichiro, Ikeda Yasumasa

机构信息

Department of Pharmacology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.

Department of Medical Pharmacology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.

出版信息

Front Cardiovasc Med. 2023 Mar 15;10:1133611. doi: 10.3389/fcvm.2023.1133611. eCollection 2023.

Abstract

Heart failure results from various physiological and pathological stimuli that lead to cardiac hypertrophy. This pathological process is common in several cardiovascular diseases and ultimately leads to heart failure. The development of cardiac hypertrophy and heart failure involves reprogramming of gene expression, a process that is highly dependent on epigenetic regulation. Histone acetylation is dynamically regulated by cardiac stress. Histone acetyltransferases play an important role in epigenetic remodeling in cardiac hypertrophy and heart failure. The regulation of histone acetyltransferases serves as a bridge between signal transduction and downstream gene reprogramming. Investigating the changes in histone acetyltransferases and histone modification sites in cardiac hypertrophy and heart failure will provide new therapeutic strategies to treat these diseases. This review summarizes the association of histone acetylation sites and histone acetylases with cardiac hypertrophy and heart failure, with emphasis on histone acetylation sites.

摘要

心力衰竭由多种导致心脏肥大的生理和病理刺激引起。这种病理过程在几种心血管疾病中很常见,并最终导致心力衰竭。心脏肥大和心力衰竭的发展涉及基因表达重编程,这一过程高度依赖表观遗传调控。组蛋白乙酰化受心脏应激动态调节。组蛋白乙酰转移酶在心脏肥大和心力衰竭的表观遗传重塑中起重要作用。组蛋白乙酰转移酶的调控充当信号转导与下游基因重编程之间的桥梁。研究心脏肥大和心力衰竭中组蛋白乙酰转移酶及组蛋白修饰位点的变化将为治疗这些疾病提供新的治疗策略。本综述总结了组蛋白乙酰化位点和组蛋白乙酰化酶与心脏肥大和心力衰竭的关联,重点是组蛋白乙酰化位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fcc/10050342/0e3665ee3d93/fcvm-10-1133611-g001.jpg

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