Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, 04100 Latina, Italy.
Department of AngioCardioNeurology, IRCCS Neuromed, 86077 Pozzilli, Italy.
Annu Rev Physiol. 2018 Feb 10;80:1-26. doi: 10.1146/annurev-physiol-021317-121427. Epub 2017 Oct 25.
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.
自噬是一种进化上保守的机制,通过该机制细胞质成分在细胞内被降解。自噬也已成为心脏内稳态和功能的主要调节者。自噬在基线条件下维持心脏结构和功能,并在应激时被激活,在大多数情况下限制损伤。它可减少缺血时的损伤并维持心脏功能。它还通过限制错误折叠蛋白积累、线粒体功能障碍和氧化应激来减轻慢性缺血性重构,并介导心脏对压力超负荷的适应。自噬的损伤参与了糖尿病和衰老引起的心脏异常的发生。自噬缺陷导致心脏蛋白病和多柔比星诱导的心肌病的发生。然而,在某些应激条件下,如再灌注损伤,大量激活自噬可能对心脏有害。在这篇综述中,我们讨论了支持自噬和线粒体自噬在调节心脏内稳态和适应应激方面的重要作用的最新证据。