Liu Jiangen, Song Xianjing, Yan Youyou, Liu Bin
Department of Cardiology, The Second Hospital of Jilin University, Changchun, China.
Front Cardiovasc Med. 2021 Sep 30;8:720085. doi: 10.3389/fcvm.2021.720085. eCollection 2021.
Heart function maintenance requires a large amount of energy, which is supplied by the mitochondria. In addition to providing energy to cardiomyocytes, mitochondria also play an important role in maintaining cell function and homeostasis. Although adult cardiomyocyte mitochondria appear as independent, low-static organelles, morphological changes have been observed in cardiomyocyte mitochondria under stress or pathological conditions. Indeed, cardiac mitochondrial fission and fusion are involved in the occurrence and development of heart diseases. As mitochondrial fission and fusion are primarily regulated by mitochondrial dynamins in a GTPase-dependent manner, GTPase-dependent mitochondrial fusion (MFN1, MFN2, and OPA1) and fission (DRP1) proteins, which are abundant in the adult heart, can also be regulated in heart diseases. In fact, these dynamic proteins have been shown to play important roles in specific diseases, including ischemia-reperfusion injury, heart failure, and metabolic cardiomyopathy. This article reviews the role of GTPase-dependent mitochondrial fusion and fission protein-mediated mitochondrial dynamics in the occurrence and development of heart diseases.
心脏功能的维持需要大量能量,这些能量由线粒体提供。除了为心肌细胞提供能量外,线粒体在维持细胞功能和内环境稳定方面也发挥着重要作用。尽管成年心肌细胞线粒体表现为独立的、低静态的细胞器,但在应激或病理条件下,心肌细胞线粒体已观察到形态变化。事实上,心脏线粒体的分裂和融合参与了心脏病的发生和发展。由于线粒体的分裂和融合主要由动力蛋白以GTP酶依赖的方式调节,在成年心脏中丰富的GTP酶依赖的线粒体融合(MFN1、MFN2和OPA1)和分裂(DRP1)蛋白,在心脏病中也可受到调节。实际上,这些动态蛋白已被证明在特定疾病中发挥重要作用,包括缺血再灌注损伤、心力衰竭和代谢性心肌病。本文综述了GTP酶依赖的线粒体融合和分裂蛋白介导的线粒体动力学在心脏病发生和发展中的作用。