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Remodeling of Mitochondrial Flashes in Muscular Development and Dystrophy in Zebrafish

Mitochondrial flash (mitoflash) is a highly-conserved, universal, and physiological mitochondrial activity in isolated mitochondria, intact cells, and live organisms. Here we investigated developmental and disease-related remodeling of mitoflash activity in zebrafish skeletal muscles. In transgenic...

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Autores principales: Zhang, Meiling, Sun, Tao, Jian, Chongshu, Lei, Lei, Han, Peidong, Lv, Quanlong, Yang, Ran, Zhou, Xiaohai, Xu, Jiejia, Hu, Yingchun, Men, Yongfan, Huang, Yanyi, Zhang, Chuanmao, Zhu, Xiaojun, Wang, Xianhua, Cheng, Heping, Xiong, Jing-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506073/
https://www.ncbi.nlm.nih.gov/pubmed/26186000
http://dx.doi.org/10.1371/journal.pone.0132567
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author Zhang, Meiling
Sun, Tao
Jian, Chongshu
Lei, Lei
Han, Peidong
Lv, Quanlong
Yang, Ran
Zhou, Xiaohai
Xu, Jiejia
Hu, Yingchun
Men, Yongfan
Huang, Yanyi
Zhang, Chuanmao
Zhu, Xiaojun
Wang, Xianhua
Cheng, Heping
Xiong, Jing-Wei
author_facet Zhang, Meiling
Sun, Tao
Jian, Chongshu
Lei, Lei
Han, Peidong
Lv, Quanlong
Yang, Ran
Zhou, Xiaohai
Xu, Jiejia
Hu, Yingchun
Men, Yongfan
Huang, Yanyi
Zhang, Chuanmao
Zhu, Xiaojun
Wang, Xianhua
Cheng, Heping
Xiong, Jing-Wei
author_sort Zhang, Meiling
collection PubMed
description Mitochondrial flash (mitoflash) is a highly-conserved, universal, and physiological mitochondrial activity in isolated mitochondria, intact cells, and live organisms. Here we investigated developmental and disease-related remodeling of mitoflash activity in zebrafish skeletal muscles. In transgenic zebrafish expressing the mitoflash reporter cpYFP, in vivo imaging revealed that mitoflash frequency and unitary properties underwent multiphasic and muscle type-specific changes, accompanying mitochondrial morphogenesis from 2 to 14 dpf. In particular, short (S)-type mitoflashes predominated in early muscle formation, then S-, transitory (T)- and regular (R)-type mitoflashes coexisted during muscle maturation, followed by a switch to R-type mitoflashes in mature skeletal muscles. In early development of muscular dystrophy, we found accelerated S- to R-type mitoflash transition and reduced mitochondrial NAD(P)H amidst a remarkable cell-to-cell heterogeneity. This study not only unravels a profound functional and morphological remodeling of mitochondria in developing and diseased skeletal muscles, but also underscores mitoflashes as a useful reporter of mitochondrial function in milieu of live animals under physiological and pathophysiological conditions.
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spelling pubmed-45060732015-07-23 Remodeling of Mitochondrial Flashes in Muscular Development and Dystrophy in Zebrafish Zhang, Meiling Sun, Tao Jian, Chongshu Lei, Lei Han, Peidong Lv, Quanlong Yang, Ran Zhou, Xiaohai Xu, Jiejia Hu, Yingchun Men, Yongfan Huang, Yanyi Zhang, Chuanmao Zhu, Xiaojun Wang, Xianhua Cheng, Heping Xiong, Jing-Wei PLoS One Research Article Mitochondrial flash (mitoflash) is a highly-conserved, universal, and physiological mitochondrial activity in isolated mitochondria, intact cells, and live organisms. Here we investigated developmental and disease-related remodeling of mitoflash activity in zebrafish skeletal muscles. In transgenic zebrafish expressing the mitoflash reporter cpYFP, in vivo imaging revealed that mitoflash frequency and unitary properties underwent multiphasic and muscle type-specific changes, accompanying mitochondrial morphogenesis from 2 to 14 dpf. In particular, short (S)-type mitoflashes predominated in early muscle formation, then S-, transitory (T)- and regular (R)-type mitoflashes coexisted during muscle maturation, followed by a switch to R-type mitoflashes in mature skeletal muscles. In early development of muscular dystrophy, we found accelerated S- to R-type mitoflash transition and reduced mitochondrial NAD(P)H amidst a remarkable cell-to-cell heterogeneity. This study not only unravels a profound functional and morphological remodeling of mitochondria in developing and diseased skeletal muscles, but also underscores mitoflashes as a useful reporter of mitochondrial function in milieu of live animals under physiological and pathophysiological conditions. Public Library of Science 2015-07-17 /pmc/articles/PMC4506073/ /pubmed/26186000 http://dx.doi.org/10.1371/journal.pone.0132567 Text en © 2015 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhang, Meiling
Sun, Tao
Jian, Chongshu
Lei, Lei
Han, Peidong
Lv, Quanlong
Yang, Ran
Zhou, Xiaohai
Xu, Jiejia
Hu, Yingchun
Men, Yongfan
Huang, Yanyi
Zhang, Chuanmao
Zhu, Xiaojun
Wang, Xianhua
Cheng, Heping
Xiong, Jing-Wei
Remodeling of Mitochondrial Flashes in Muscular Development and Dystrophy in Zebrafish
title Remodeling of Mitochondrial Flashes in Muscular Development and Dystrophy in Zebrafish
title_full Remodeling of Mitochondrial Flashes in Muscular Development and Dystrophy in Zebrafish
title_fullStr Remodeling of Mitochondrial Flashes in Muscular Development and Dystrophy in Zebrafish
title_full_unstemmed Remodeling of Mitochondrial Flashes in Muscular Development and Dystrophy in Zebrafish
title_short Remodeling of Mitochondrial Flashes in Muscular Development and Dystrophy in Zebrafish
title_sort remodeling of mitochondrial flashes in muscular development and dystrophy in zebrafish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506073/
https://www.ncbi.nlm.nih.gov/pubmed/26186000
http://dx.doi.org/10.1371/journal.pone.0132567
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