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Exercise induces new cardiomyocyte generation in the adult mammalian heart
Loss of cardiomyocytes is a major cause of heart failure, and while the adult heart has a limited capacity for cardiomyogenesis, little is known about what regulates this ability or whether it can be effectively harnessed. Here we show that 8 weeks of running exercise increase birth of new cardiomyo...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916892/ https://www.ncbi.nlm.nih.gov/pubmed/29695718 http://dx.doi.org/10.1038/s41467-018-04083-1 |
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author | Vujic, Ana Lerchenmüller, Carolin Wu, Ting-Di Guillermier, Christelle Rabolli, Charles P. Gonzalez, Emilia Senyo, Samuel E. Liu, Xiaojun Guerquin-Kern, Jean-Luc Steinhauser, Matthew L. Lee, Richard T. Rosenzweig, Anthony |
author_facet | Vujic, Ana Lerchenmüller, Carolin Wu, Ting-Di Guillermier, Christelle Rabolli, Charles P. Gonzalez, Emilia Senyo, Samuel E. Liu, Xiaojun Guerquin-Kern, Jean-Luc Steinhauser, Matthew L. Lee, Richard T. Rosenzweig, Anthony |
author_sort | Vujic, Ana |
collection | PubMed |
description | Loss of cardiomyocytes is a major cause of heart failure, and while the adult heart has a limited capacity for cardiomyogenesis, little is known about what regulates this ability or whether it can be effectively harnessed. Here we show that 8 weeks of running exercise increase birth of new cardiomyocytes in adult mice (~4.6-fold). New cardiomyocytes are identified based on incorporation of (15)N-thymidine by multi-isotope imaging mass spectrometry (MIMS) and on being mononucleate/diploid. Furthermore, we demonstrate that exercise after myocardial infarction induces a robust cardiomyogenic response in an extended border zone of the infarcted area. Inhibition of miR-222, a microRNA increased by exercise in both animal models and humans, completely blocks the cardiomyogenic exercise response. These findings demonstrate that cardiomyogenesis can be activated by exercise in the normal and injured adult mouse heart and suggest that stimulation of endogenous cardiomyocyte generation could contribute to the benefits of exercise. |
format | Online Article Text |
id | pubmed-5916892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59168922018-04-27 Exercise induces new cardiomyocyte generation in the adult mammalian heart Vujic, Ana Lerchenmüller, Carolin Wu, Ting-Di Guillermier, Christelle Rabolli, Charles P. Gonzalez, Emilia Senyo, Samuel E. Liu, Xiaojun Guerquin-Kern, Jean-Luc Steinhauser, Matthew L. Lee, Richard T. Rosenzweig, Anthony Nat Commun Article Loss of cardiomyocytes is a major cause of heart failure, and while the adult heart has a limited capacity for cardiomyogenesis, little is known about what regulates this ability or whether it can be effectively harnessed. Here we show that 8 weeks of running exercise increase birth of new cardiomyocytes in adult mice (~4.6-fold). New cardiomyocytes are identified based on incorporation of (15)N-thymidine by multi-isotope imaging mass spectrometry (MIMS) and on being mononucleate/diploid. Furthermore, we demonstrate that exercise after myocardial infarction induces a robust cardiomyogenic response in an extended border zone of the infarcted area. Inhibition of miR-222, a microRNA increased by exercise in both animal models and humans, completely blocks the cardiomyogenic exercise response. These findings demonstrate that cardiomyogenesis can be activated by exercise in the normal and injured adult mouse heart and suggest that stimulation of endogenous cardiomyocyte generation could contribute to the benefits of exercise. Nature Publishing Group UK 2018-04-25 /pmc/articles/PMC5916892/ /pubmed/29695718 http://dx.doi.org/10.1038/s41467-018-04083-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Vujic, Ana Lerchenmüller, Carolin Wu, Ting-Di Guillermier, Christelle Rabolli, Charles P. Gonzalez, Emilia Senyo, Samuel E. Liu, Xiaojun Guerquin-Kern, Jean-Luc Steinhauser, Matthew L. Lee, Richard T. Rosenzweig, Anthony Exercise induces new cardiomyocyte generation in the adult mammalian heart |
title | Exercise induces new cardiomyocyte generation in the adult mammalian heart |
title_full | Exercise induces new cardiomyocyte generation in the adult mammalian heart |
title_fullStr | Exercise induces new cardiomyocyte generation in the adult mammalian heart |
title_full_unstemmed | Exercise induces new cardiomyocyte generation in the adult mammalian heart |
title_short | Exercise induces new cardiomyocyte generation in the adult mammalian heart |
title_sort | exercise induces new cardiomyocyte generation in the adult mammalian heart |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916892/ https://www.ncbi.nlm.nih.gov/pubmed/29695718 http://dx.doi.org/10.1038/s41467-018-04083-1 |
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