自噬
粒体自噬
细胞生物学
平衡
心功能曲线
细胞适应
调节器
心肌病
氧化应激
缺血
机制(生物学)
线粒体
再灌注损伤
心力衰竭
生物
内科学
医学
内分泌学
生物化学
细胞凋亡
哲学
认识论
基因
作者
Sebastiano Sciarretta,Yasuhiro Maejima,Daniela Zablocki,Junichi Sadoshima
出处
期刊:Annual Review of Physiology
[Annual Reviews]
日期:2018-02-10
卷期号:80 (1): 1-26
被引量:326
标识
DOI:10.1146/annurev-physiol-021317-121427
摘要
Autophagy is an evolutionarily conserved mechanism by which cytoplasmic elements are degraded intracellularly. Autophagy has also emerged as a major regulator of cardiac homeostasis and function. Autophagy preserves cardiac structure and function under baseline conditions and is activated during stress, limiting damage under most conditions. It reduces injury and preserves cardiac function during ischemia. It also reduces chronic ischemic remodeling and mediates the cardiac adaptation to pressure overload by restricting misfolded protein accumulation, mitochondrial dysfunction, and oxidative stress. Impairment of autophagy is involved in the development of diabetes and aging-induced cardiac abnormalities. Autophagy defects contribute to the development of cardiac proteinopathy and doxorubicin-induced cardiomyopathy. However, massive activation of autophagy may be detrimental for the heart in certain stress conditions, such as reperfusion injury. In this review, we discuss recent evidence supporting the important role of autophagy and mitophagy in the regulation of cardiac homeostasis and adaptation to stress.
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