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Regulatory Mechanisms of Mitochondrial Function and Cardiac Aging

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 dysfunctio...

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Autores principales: Lin, Ruizhu, Kerkelä, Risto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072955/
https://www.ncbi.nlm.nih.gov/pubmed/32085438
http://dx.doi.org/10.3390/ijms21041359
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author Lin, Ruizhu
Kerkelä, Risto
author_facet Lin, Ruizhu
Kerkelä, Risto
author_sort Lin, Ruizhu
collection PubMed
description 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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spelling pubmed-70729552020-03-19 Regulatory Mechanisms of Mitochondrial Function and Cardiac Aging Lin, Ruizhu Kerkelä, Risto Int J Mol Sci Review 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. MDPI 2020-02-18 /pmc/articles/PMC7072955/ /pubmed/32085438 http://dx.doi.org/10.3390/ijms21041359 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Lin, Ruizhu
Kerkelä, Risto
Regulatory Mechanisms of Mitochondrial Function and Cardiac Aging
title Regulatory Mechanisms of Mitochondrial Function and Cardiac Aging
title_full Regulatory Mechanisms of Mitochondrial Function and Cardiac Aging
title_fullStr Regulatory Mechanisms of Mitochondrial Function and Cardiac Aging
title_full_unstemmed Regulatory Mechanisms of Mitochondrial Function and Cardiac Aging
title_short Regulatory Mechanisms of Mitochondrial Function and Cardiac Aging
title_sort regulatory mechanisms of mitochondrial function and cardiac aging
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072955/
https://www.ncbi.nlm.nih.gov/pubmed/32085438
http://dx.doi.org/10.3390/ijms21041359
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