Liang Wenjing J, Gustafsson Åsa B
Department of Pharmacology, Department of Medicine, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, CA, United States.
Front Cardiovasc Med. 2020 Feb 19;7:18. doi: 10.3389/fcvm.2020.00018. eCollection 2020.
Aging is associated with structural and functional changes in the heart and is a major risk factor in developing cardiovascular disease. Many recent studies have focused on increasing our understanding of the basis of aging at the cellular and molecular levels in various tissues, including the heart. It is known that there is an age-related decline in cellular quality control pathways such as autophagy and mitophagy, which leads to accumulation of potentially harmful cellular components in cardiac myocytes. There is evidence that diminished autophagy and mitophagy accelerate the aging process, while enhancement preserves cardiac homeostasis and extends life span. Here, we review the current knowledge of autophagy and mitophagy in aging and discuss how age-associated alterations in these processes contribute to cardiac aging and age-related cardiovascular diseases.
衰老与心脏的结构和功能变化相关,是心血管疾病发生的主要风险因素。最近的许多研究都集中在增进我们对包括心脏在内的各种组织在细胞和分子水平上衰老基础的理解。众所周知,自噬和线粒体自噬等细胞质量控制途径会随着年龄增长而衰退,这导致心肌细胞中潜在有害的细胞成分积累。有证据表明,自噬和线粒体自噬的减弱会加速衰老过程,而增强这些过程则能维持心脏内环境稳定并延长寿命。在此,我们综述了目前关于衰老过程中自噬和线粒体自噬的知识,并讨论这些过程中与年龄相关的改变如何导致心脏衰老和年龄相关的心血管疾病。