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Mild cold induced thermogenesis: are BAT and skeletal muscle synergistic partners?
There are two well-described thermogenic sites; brown adipose tissue (BAT) and skeletal muscle, which utilize distinct mechanisms of heat production. In BAT, mitochondrial metabolism is the molecular basis of heat generation, while it serves only a secondary role in supplying energy for thermogenesi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617911/ https://www.ncbi.nlm.nih.gov/pubmed/28831023 http://dx.doi.org/10.1042/BSR20171087 |
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author | Bal, Naresh C. Maurya, Santosh K. Pani, Sunil Sethy, Chinmayee Banerjee, Ananya Das, Sarita Patnaik, Srinivas Kundu, Chanakya N. |
author_facet | Bal, Naresh C. Maurya, Santosh K. Pani, Sunil Sethy, Chinmayee Banerjee, Ananya Das, Sarita Patnaik, Srinivas Kundu, Chanakya N. |
author_sort | Bal, Naresh C. |
collection | PubMed |
description | There are two well-described thermogenic sites; brown adipose tissue (BAT) and skeletal muscle, which utilize distinct mechanisms of heat production. In BAT, mitochondrial metabolism is the molecular basis of heat generation, while it serves only a secondary role in supplying energy for thermogenesis in muscle. Here, we wanted to document changes in mitochondrial ultrastructure in these two tissue types based upon adaptation to mild (16°C) and severe (4°C) cold in mice. When reared at thermoneutrality (29°C), mitochondria in both tissues were loosely packed with irregular cristae. Interestingly, adaptation to even mild cold initiated ultrastructural remodeling of mitochondria including acquisition of more elaborate cristae structure in both thermogenic sites. The shape of mitochondria in the BAT remained mostly circular, whereas the intermyofibrilar mitochondria in the skeletal muscle became more elongated and tubular. The most dramatic remodeling of mitochondrial architecture was observed upon adaptation to severe cold. In addition, we report cold-induced alteration in levels of humoral factors: fibroblast growth factor 21 (FGF21), IL1α, peptide YY (PYY), tumor necrosis factor α (TNFα), and interleukin 6 (IL6) were all induced whereas both insulin and leptin were down-regulated. In summary, adaptation to cold leads to enhanced cristae formation in mitochondria in skeletal muscle as well as the BAT. Further, the present study indicates that circulating cytokines might play an important role in the synergistic recruitment of the thermogenic program including cross-talk between muscle and BAT. |
format | Online Article Text |
id | pubmed-5617911 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56179112017-10-10 Mild cold induced thermogenesis: are BAT and skeletal muscle synergistic partners? Bal, Naresh C. Maurya, Santosh K. Pani, Sunil Sethy, Chinmayee Banerjee, Ananya Das, Sarita Patnaik, Srinivas Kundu, Chanakya N. Biosci Rep Research Articles There are two well-described thermogenic sites; brown adipose tissue (BAT) and skeletal muscle, which utilize distinct mechanisms of heat production. In BAT, mitochondrial metabolism is the molecular basis of heat generation, while it serves only a secondary role in supplying energy for thermogenesis in muscle. Here, we wanted to document changes in mitochondrial ultrastructure in these two tissue types based upon adaptation to mild (16°C) and severe (4°C) cold in mice. When reared at thermoneutrality (29°C), mitochondria in both tissues were loosely packed with irregular cristae. Interestingly, adaptation to even mild cold initiated ultrastructural remodeling of mitochondria including acquisition of more elaborate cristae structure in both thermogenic sites. The shape of mitochondria in the BAT remained mostly circular, whereas the intermyofibrilar mitochondria in the skeletal muscle became more elongated and tubular. The most dramatic remodeling of mitochondrial architecture was observed upon adaptation to severe cold. In addition, we report cold-induced alteration in levels of humoral factors: fibroblast growth factor 21 (FGF21), IL1α, peptide YY (PYY), tumor necrosis factor α (TNFα), and interleukin 6 (IL6) were all induced whereas both insulin and leptin were down-regulated. In summary, adaptation to cold leads to enhanced cristae formation in mitochondria in skeletal muscle as well as the BAT. Further, the present study indicates that circulating cytokines might play an important role in the synergistic recruitment of the thermogenic program including cross-talk between muscle and BAT. Portland Press Ltd. 2017-09-28 /pmc/articles/PMC5617911/ /pubmed/28831023 http://dx.doi.org/10.1042/BSR20171087 Text en © 2017 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Articles Bal, Naresh C. Maurya, Santosh K. Pani, Sunil Sethy, Chinmayee Banerjee, Ananya Das, Sarita Patnaik, Srinivas Kundu, Chanakya N. Mild cold induced thermogenesis: are BAT and skeletal muscle synergistic partners? |
title | Mild cold induced thermogenesis: are BAT and skeletal muscle synergistic partners? |
title_full | Mild cold induced thermogenesis: are BAT and skeletal muscle synergistic partners? |
title_fullStr | Mild cold induced thermogenesis: are BAT and skeletal muscle synergistic partners? |
title_full_unstemmed | Mild cold induced thermogenesis: are BAT and skeletal muscle synergistic partners? |
title_short | Mild cold induced thermogenesis: are BAT and skeletal muscle synergistic partners? |
title_sort | mild cold induced thermogenesis: are bat and skeletal muscle synergistic partners? |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617911/ https://www.ncbi.nlm.nih.gov/pubmed/28831023 http://dx.doi.org/10.1042/BSR20171087 |
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