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Mitochondrial dynamism and heart disease: changing shape and shaping change

Mitochondria of adult cardiomyocytes appear hypo-dynamic, lacking interconnected reticular networks and the continual fission and fusion observed in many other cell types. Nevertheless, proteins essential to mitochondrial network remodeling are abundant in adult hearts. Recent findings from cardiac-...

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Autor principal: Dorn II, Gerald W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4520653/
https://www.ncbi.nlm.nih.gov/pubmed/25861797
http://dx.doi.org/10.15252/emmm.201404575
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author Dorn II, Gerald W
author_facet Dorn II, Gerald W
author_sort Dorn II, Gerald W
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description Mitochondria of adult cardiomyocytes appear hypo-dynamic, lacking interconnected reticular networks and the continual fission and fusion observed in many other cell types. Nevertheless, proteins essential to mitochondrial network remodeling are abundant in adult hearts. Recent findings from cardiac-specific ablation of mitochondrial fission and fusion protein genes have revealed unexpected roles for mitochondrial dynamics factors in mitophagic mitochondrial quality control. This overview examines the clinical and experimental evidence for and against a meaningful role for the mitochondrial dynamism–quality control interactome in normal and diseased hearts. Newly discovered functions of mitochondrial dynamics factors in maintaining optimal cardiac mitochondrial fitness suggest that deep interrogation of clinical cardiomyopathy is likely to reveal genetic variants that cause or modify cardiac disease through their effects on mitochondrial fission, fusion, and mitophagy.
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spelling pubmed-45206532015-08-05 Mitochondrial dynamism and heart disease: changing shape and shaping change Dorn II, Gerald W EMBO Mol Med Reviews Mitochondria of adult cardiomyocytes appear hypo-dynamic, lacking interconnected reticular networks and the continual fission and fusion observed in many other cell types. Nevertheless, proteins essential to mitochondrial network remodeling are abundant in adult hearts. Recent findings from cardiac-specific ablation of mitochondrial fission and fusion protein genes have revealed unexpected roles for mitochondrial dynamics factors in mitophagic mitochondrial quality control. This overview examines the clinical and experimental evidence for and against a meaningful role for the mitochondrial dynamism–quality control interactome in normal and diseased hearts. Newly discovered functions of mitochondrial dynamics factors in maintaining optimal cardiac mitochondrial fitness suggest that deep interrogation of clinical cardiomyopathy is likely to reveal genetic variants that cause or modify cardiac disease through their effects on mitochondrial fission, fusion, and mitophagy. John Wiley & Sons, Ltd 2015-07 2015-04-10 /pmc/articles/PMC4520653/ /pubmed/25861797 http://dx.doi.org/10.15252/emmm.201404575 Text en © 2015 The Author. Published under the terms of the CC BY 4.0 license http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Dorn II, Gerald W
Mitochondrial dynamism and heart disease: changing shape and shaping change
title Mitochondrial dynamism and heart disease: changing shape and shaping change
title_full Mitochondrial dynamism and heart disease: changing shape and shaping change
title_fullStr Mitochondrial dynamism and heart disease: changing shape and shaping change
title_full_unstemmed Mitochondrial dynamism and heart disease: changing shape and shaping change
title_short Mitochondrial dynamism and heart disease: changing shape and shaping change
title_sort mitochondrial dynamism and heart disease: changing shape and shaping change
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4520653/
https://www.ncbi.nlm.nih.gov/pubmed/25861797
http://dx.doi.org/10.15252/emmm.201404575
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