Linton Phyllis-Jean, Gurney Michael, Sengstock David, Mentzer Robert M, Gottlieb Roberta A
Donald P. Shiley BioScience Center, San Diego State University, San Diego, CA, USA.
Division of Geriatric Medicine, Oakwood Hospital, Dearborn, MI, USA; Department of Internal Medicine, Wayne State University School of Medicine, Detroit, MI, USA.
J Mol Cell Cardiol. 2015 Jun;83:44-54. doi: 10.1016/j.yjmcc.2014.12.017. Epub 2014 Dec 24.
Autophagy, a cellular housekeeping process, is essential to maintain tissue homeostasis, particularly in long-lived cells such as cardiomyocytes. Autophagic activity declines with age and may explain many features of age-related cardiac dysfunction. In this review we summarize the current state of knowledge regarding age-related changes in autophagy in the heart. Recent findings from studies in human hearts are presented, including evidence that the autophagic response is intact in the aged human heart. Impaired autophagic clearance of protein aggregates or deteriorating mitochondria will have multiple consequences including increased arrhythmia risk, decreased contractile function, reduced tolerance to ischemic stress, and increased inflammation; thus autophagy represents a potentially important therapeutic target to mitigate the cardiac consequences of aging. This article is part of a Special Issue entitled CV Aging.
自噬是一种细胞清理过程,对于维持组织内稳态至关重要,尤其是在心肌细胞等长寿细胞中。自噬活性会随着年龄增长而下降,这可能解释了与年龄相关的心脏功能障碍的许多特征。在这篇综述中,我们总结了目前关于心脏自噬随年龄变化的知识现状。文中呈现了近期对人类心脏研究的发现,包括有证据表明老年人类心脏中的自噬反应是完整的。蛋白质聚集体或受损线粒体的自噬清除受损会产生多种后果,包括心律失常风险增加、收缩功能下降、对缺血应激的耐受性降低以及炎症增加;因此,自噬是减轻衰老对心脏影响的一个潜在重要治疗靶点。本文是名为“心血管衰老”的特刊的一部分。