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Mitophagy is required for brown adipose tissue mitochondrial homeostasis during cold challenge
Brown adipose tissue (BAT) is a specialized thermogenic organ in mammals. The ability of BAT mitochondria to generate heat in response to cold-challenge to maintain core body temperature is essential for organismal survival. While cold activated BAT mitochondrial biogenesis is recognized as critical...
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/PMC5974273/ https://www.ncbi.nlm.nih.gov/pubmed/29844467 http://dx.doi.org/10.1038/s41598-018-26394-5 |
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author | Lu, Yuan Fujioka, Hisashi Joshi, Dinesh Li, Qiaoyuan Sangwung, Panjamaporn Hsieh, Paishiun Zhu, Jiyun Torio, Jose Sweet, David Wang, Lan Chiu, Shing Yan Croniger, Colleen Liao, Xudong Jain, Mukesh K. |
author_facet | Lu, Yuan Fujioka, Hisashi Joshi, Dinesh Li, Qiaoyuan Sangwung, Panjamaporn Hsieh, Paishiun Zhu, Jiyun Torio, Jose Sweet, David Wang, Lan Chiu, Shing Yan Croniger, Colleen Liao, Xudong Jain, Mukesh K. |
author_sort | Lu, Yuan |
collection | PubMed |
description | Brown adipose tissue (BAT) is a specialized thermogenic organ in mammals. The ability of BAT mitochondria to generate heat in response to cold-challenge to maintain core body temperature is essential for organismal survival. While cold activated BAT mitochondrial biogenesis is recognized as critical for thermogenic adaptation, the contribution of mitochondrial quality control to this process remains unclear. Here, we show mitophagy is required for brown adipocyte mitochondrial homeostasis during thermogenic adaptation. Mitophagy is significantly increased in BAT from cold-challenged mice (4 °C) and in β-agonist treated brown adipocytes. Blockade of mitophagy compromises brown adipocytes mitochondrial oxidative phosphorylation (OX-PHOS) capacity, as well as BAT mitochondrial integrity. Mechanistically, cold-challenge induction of BAT mitophagy is UCP1-dependent. Furthermore, our results indicate that mitophagy coordinates with mitochondrial biogenesis, maintaining activated BAT mitochondrial homeostasis. Collectively, our in vivo and in vitro findings identify mitophagy as critical for brown adipocyte mitochondrial homeostasis during cold adaptation. |
format | Online Article Text |
id | pubmed-5974273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59742732018-05-31 Mitophagy is required for brown adipose tissue mitochondrial homeostasis during cold challenge Lu, Yuan Fujioka, Hisashi Joshi, Dinesh Li, Qiaoyuan Sangwung, Panjamaporn Hsieh, Paishiun Zhu, Jiyun Torio, Jose Sweet, David Wang, Lan Chiu, Shing Yan Croniger, Colleen Liao, Xudong Jain, Mukesh K. Sci Rep Article Brown adipose tissue (BAT) is a specialized thermogenic organ in mammals. The ability of BAT mitochondria to generate heat in response to cold-challenge to maintain core body temperature is essential for organismal survival. While cold activated BAT mitochondrial biogenesis is recognized as critical for thermogenic adaptation, the contribution of mitochondrial quality control to this process remains unclear. Here, we show mitophagy is required for brown adipocyte mitochondrial homeostasis during thermogenic adaptation. Mitophagy is significantly increased in BAT from cold-challenged mice (4 °C) and in β-agonist treated brown adipocytes. Blockade of mitophagy compromises brown adipocytes mitochondrial oxidative phosphorylation (OX-PHOS) capacity, as well as BAT mitochondrial integrity. Mechanistically, cold-challenge induction of BAT mitophagy is UCP1-dependent. Furthermore, our results indicate that mitophagy coordinates with mitochondrial biogenesis, maintaining activated BAT mitochondrial homeostasis. Collectively, our in vivo and in vitro findings identify mitophagy as critical for brown adipocyte mitochondrial homeostasis during cold adaptation. Nature Publishing Group UK 2018-05-29 /pmc/articles/PMC5974273/ /pubmed/29844467 http://dx.doi.org/10.1038/s41598-018-26394-5 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 Lu, Yuan Fujioka, Hisashi Joshi, Dinesh Li, Qiaoyuan Sangwung, Panjamaporn Hsieh, Paishiun Zhu, Jiyun Torio, Jose Sweet, David Wang, Lan Chiu, Shing Yan Croniger, Colleen Liao, Xudong Jain, Mukesh K. Mitophagy is required for brown adipose tissue mitochondrial homeostasis during cold challenge |
title | Mitophagy is required for brown adipose tissue mitochondrial homeostasis during cold challenge |
title_full | Mitophagy is required for brown adipose tissue mitochondrial homeostasis during cold challenge |
title_fullStr | Mitophagy is required for brown adipose tissue mitochondrial homeostasis during cold challenge |
title_full_unstemmed | Mitophagy is required for brown adipose tissue mitochondrial homeostasis during cold challenge |
title_short | Mitophagy is required for brown adipose tissue mitochondrial homeostasis during cold challenge |
title_sort | mitophagy is required for brown adipose tissue mitochondrial homeostasis during cold challenge |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974273/ https://www.ncbi.nlm.nih.gov/pubmed/29844467 http://dx.doi.org/10.1038/s41598-018-26394-5 |
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