Key result
This review summarizes recent findings regarding key factors regulating cellular senescence, mitochondrial health, and cardiomyocyte rejuvenation in the context of cardiac aging.
Why the study?
The causes and consequences of cardiac senescence during aging or cardiac pathologies are mostly unrecognized, and targeted cell types and structural/functional effects of anti-senescence therapies remain largely overlooked.
This review highlights the need to consider the unique functional properties of cardiomyocytes when designing anti-senescence therapeutics for cardiac aging.
May guide research on senescence and mitochondria in cardiac aging; leaves open clinical translation pending trials.
Aging is a major risk factor for cardiovascular diseases (CVDs), the major cause of death worldwide. Cardiac myocytes, which hold the most abundant mitochondrial population, are terminally differentiated cells with diminished regenerative capacity in the adult. Cardiomyocyte mitochondrial dysfunction is a characteristic feature of the aging heart and one out of the nine features of cellular aging. Aging and cardiac pathologies are also associated with increased senescence in the heart. However, the cause and consequences of cardiac senescence during aging or in cardiac pathologies are mostly unrecognized. Further, despite recent advancement in anti-senescence therapy, the targeted cell type and the effect on cardiac structure and function have been largely overlooked. The unique cellular composition of the heart, and especially the functional properties of cardiomyocytes, need to be considered when designing therapeutics to target cardiac aging. Here we review recent findings regarding key factors regulating cell senescence, mitochondrial health as well as cardiomyocyte rejuvenation.
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Lin et al. (2020) conducted a review in Cardiac aging. This review summarizes recent findings regarding key factors regulating cellular senescence, mitochondrial health, and cardiomyocyte rejuvenation in the context of cardiac aging.
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