Department of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, Rutgers New Jersey Medical School, Newark, New Jersey, USA.
University of California San Diego, Department of Pharmacology, La Jolla, California, USA.
Compr Physiol. 2017 Sep 12;7(4):1407-1424. doi: 10.1002/cphy.c170005.
Mitochondria are dynamic organelles that can undergo fusion, fission, biogenesis, and autophagic elimination to maintain mitochondrial quality control. Since the heart is in constant need of high amounts of energy, mitochondria, as a central energy supply source, play a crucial role in maintaining optimal cardiac performance. Therefore, it is reasonable to assume that mitochondrial dysfunction is associated with the pathophysiology of heart diseases. In non-dividing, post-mitotic cells such as cardiomyocytes, elimination of dysfunctional organelles is essential to maintaining cellular function because non-dividing cells cannot dilute dysfunctional organelles through cell division. In this review, we discuss the recent findings regarding the physiological role of mitophagy in the heart and cardiomyocytes. Moreover, we discuss the functional role of mitophagy in the progression of cardiovascular diseases, including myocardial ischemic injury, diabetic cardiomyopathy, cardiac hypertrophy, and heart failure. © 2017 American Physiological Society. Compr Physiol 7:1407-1424, 2017.
线粒体是一种动态细胞器,能够通过融合、裂变、生物发生和自噬消除来维持线粒体的质量控制。由于心脏不断需要大量的能量,线粒体作为中央能量供应源,在维持最佳心脏功能方面起着至关重要的作用。因此,可以合理地假设线粒体功能障碍与心脏病的病理生理学有关。在非分裂、有丝分裂后的细胞(如心肌细胞)中,消除功能失调的细胞器对于维持细胞功能至关重要,因为非分裂细胞不能通过细胞分裂稀释功能失调的细胞器。在这篇综述中,我们讨论了关于自噬在线粒体和心肌细胞中的生理作用的最新发现。此外,我们还讨论了自噬在心血管疾病进展中的功能作用,包括心肌缺血损伤、糖尿病心肌病、心肌肥大和心力衰竭。