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The ω6-fatty acid, arachidonic acid, regulates the conversion of white to brite adipocyte through a prostaglandin/calcium mediated pathway
OBJECTIVE: Brite adipocytes are inducible energy-dissipating cells expressing UCP1 which appear within white adipose tissue of healthy adult individuals. Recruitment of these cells represents a potential strategy to fight obesity and associated diseases. METHODS/RESULTS: Using human Multipotent Adip...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264041/ https://www.ncbi.nlm.nih.gov/pubmed/25506549 http://dx.doi.org/10.1016/j.molmet.2014.09.003 |
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author | Pisani, Didier F. Ghandour, Rayane A. Beranger, Guillaume E. Le Faouder, Pauline Chambard, Jean-Claude Giroud, Maude Vegiopoulos, Alexandros Djedaini, Mansour Bertrand-Michel, Justine Tauc, Michel Herzig, Stephan Langin, Dominique Ailhaud, Gérard Duranton, Christophe Amri, Ez-Zoubir |
author_facet | Pisani, Didier F. Ghandour, Rayane A. Beranger, Guillaume E. Le Faouder, Pauline Chambard, Jean-Claude Giroud, Maude Vegiopoulos, Alexandros Djedaini, Mansour Bertrand-Michel, Justine Tauc, Michel Herzig, Stephan Langin, Dominique Ailhaud, Gérard Duranton, Christophe Amri, Ez-Zoubir |
author_sort | Pisani, Didier F. |
collection | PubMed |
description | OBJECTIVE: Brite adipocytes are inducible energy-dissipating cells expressing UCP1 which appear within white adipose tissue of healthy adult individuals. Recruitment of these cells represents a potential strategy to fight obesity and associated diseases. METHODS/RESULTS: Using human Multipotent Adipose-Derived Stem cells, able to convert into brite adipocytes, we show that arachidonic acid strongly inhibits brite adipocyte formation via a cyclooxygenase pathway leading to secretion of PGE2 and PGF2α. Both prostaglandins induce an oscillatory Ca(++) signaling coupled to ERK pathway and trigger a decrease in UCP1 expression and in oxygen consumption without altering mitochondriogenesis. In mice fed a standard diet supplemented with ω6 arachidonic acid, PGF2α and PGE2 amounts are increased in subcutaneous white adipose tissue and associated with a decrease in the recruitment of brite adipocytes. CONCLUSION: Our results suggest that dietary excess of ω6 polyunsaturated fatty acids present in Western diets, may also favor obesity by preventing the “browning” process to take place. |
format | Online Article Text |
id | pubmed-4264041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-42640412014-12-13 The ω6-fatty acid, arachidonic acid, regulates the conversion of white to brite adipocyte through a prostaglandin/calcium mediated pathway Pisani, Didier F. Ghandour, Rayane A. Beranger, Guillaume E. Le Faouder, Pauline Chambard, Jean-Claude Giroud, Maude Vegiopoulos, Alexandros Djedaini, Mansour Bertrand-Michel, Justine Tauc, Michel Herzig, Stephan Langin, Dominique Ailhaud, Gérard Duranton, Christophe Amri, Ez-Zoubir Mol Metab Original Article OBJECTIVE: Brite adipocytes are inducible energy-dissipating cells expressing UCP1 which appear within white adipose tissue of healthy adult individuals. Recruitment of these cells represents a potential strategy to fight obesity and associated diseases. METHODS/RESULTS: Using human Multipotent Adipose-Derived Stem cells, able to convert into brite adipocytes, we show that arachidonic acid strongly inhibits brite adipocyte formation via a cyclooxygenase pathway leading to secretion of PGE2 and PGF2α. Both prostaglandins induce an oscillatory Ca(++) signaling coupled to ERK pathway and trigger a decrease in UCP1 expression and in oxygen consumption without altering mitochondriogenesis. In mice fed a standard diet supplemented with ω6 arachidonic acid, PGF2α and PGE2 amounts are increased in subcutaneous white adipose tissue and associated with a decrease in the recruitment of brite adipocytes. CONCLUSION: Our results suggest that dietary excess of ω6 polyunsaturated fatty acids present in Western diets, may also favor obesity by preventing the “browning” process to take place. Elsevier 2014-09-16 /pmc/articles/PMC4264041/ /pubmed/25506549 http://dx.doi.org/10.1016/j.molmet.2014.09.003 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Original Article Pisani, Didier F. Ghandour, Rayane A. Beranger, Guillaume E. Le Faouder, Pauline Chambard, Jean-Claude Giroud, Maude Vegiopoulos, Alexandros Djedaini, Mansour Bertrand-Michel, Justine Tauc, Michel Herzig, Stephan Langin, Dominique Ailhaud, Gérard Duranton, Christophe Amri, Ez-Zoubir The ω6-fatty acid, arachidonic acid, regulates the conversion of white to brite adipocyte through a prostaglandin/calcium mediated pathway |
title | The ω6-fatty acid, arachidonic acid, regulates the conversion of white to brite adipocyte through a prostaglandin/calcium mediated pathway |
title_full | The ω6-fatty acid, arachidonic acid, regulates the conversion of white to brite adipocyte through a prostaglandin/calcium mediated pathway |
title_fullStr | The ω6-fatty acid, arachidonic acid, regulates the conversion of white to brite adipocyte through a prostaglandin/calcium mediated pathway |
title_full_unstemmed | The ω6-fatty acid, arachidonic acid, regulates the conversion of white to brite adipocyte through a prostaglandin/calcium mediated pathway |
title_short | The ω6-fatty acid, arachidonic acid, regulates the conversion of white to brite adipocyte through a prostaglandin/calcium mediated pathway |
title_sort | ω6-fatty acid, arachidonic acid, regulates the conversion of white to brite adipocyte through a prostaglandin/calcium mediated pathway |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264041/ https://www.ncbi.nlm.nih.gov/pubmed/25506549 http://dx.doi.org/10.1016/j.molmet.2014.09.003 |
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