Abstract | OBJECTIVE: Thermogenic adipocytes (i.e. brown or brite/beige adipocytes) are able to burn large amounts of lipids and carbohydrates as a result of highly active mitochondria and enhanced uncoupled respiration, due to UCP1 activity. Although mitochondria are the key organelles for this thermogenic function, limited human data are available. METHODS/RESULTS: We characterized changes in the mitochondrial function of human brite adipocytes, using hMADS cells as a model of white- to brite-adipocyte conversion. We found that profound molecular modifications were associated with morphological changes in mitochondria. The fission process was partly driven by the DRP1 protein, which also promoted mitochondrial uncoupling. CONCLUSION: Our data demonstrate that white-to-brite conversion of human adipocytes relies on molecular, morphological and functional changes in mitochondria, which enable brite/beige cells to carry out thermogenesis.
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Authors | Didier F Pisani, Valentin Barquissau, Jean-Claude Chambard, Diane Beuzelin, Rayane A Ghandour, Maude Giroud, Aline Mairal, Sophie Pagnotta, Saverio Cinti, Dominique Langin, Ez-Zoubir Amri |
Journal | Molecular metabolism
(Mol Metab)
Vol. 7
Pg. 35-44
(01 2018)
ISSN: 2212-8778 [Electronic] Germany |
PMID | 29198749
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2017 The Authors. Published by Elsevier GmbH.. All rights reserved. |
Chemical References |
- Microtubule-Associated Proteins
- Mitochondrial Proteins
- UCP1 protein, human
- Uncoupling Protein 1
- GTP Phosphohydrolases
- DNM1L protein, human
- Dynamins
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Topics |
- Adipocytes, Beige
(metabolism, ultrastructure)
- Cells, Cultured
- Dynamins
- GTP Phosphohydrolases
(metabolism)
- Humans
- Microtubule-Associated Proteins
(metabolism)
- Mitochondrial Dynamics
- Mitochondrial Proteins
(metabolism)
- Uncoupling Protein 1
(metabolism)
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