Cargando…

Let-7i-5p represses brite adipocyte function in mice and humans

In response to cold or β3-adrenoreceptor stimulation brown adipose tissue (BAT) promotes non-shivering thermogenesis, leading to energy dissipation. BAT has long been thought to be absent or scarce in adult humans. The recent discovery of thermogenic brite/beige adipocytes has opened the way to deve...

Descripción completa

Detalles Bibliográficos
Autores principales: Giroud, Maude, Karbiener, Michael, Pisani, Didier F., Ghandour, Rayane A., Beranger, Guillaume E., Niemi, Tarja, Taittonen, Markku, Nuutila, Pirjo, Virtanen, Kirsi A., Langin, Dominique, Scheideler, Marcel, Amri, Ez-Zoubir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921928/
https://www.ncbi.nlm.nih.gov/pubmed/27345691
http://dx.doi.org/10.1038/srep28613
_version_ 1782439564414025728
author Giroud, Maude
Karbiener, Michael
Pisani, Didier F.
Ghandour, Rayane A.
Beranger, Guillaume E.
Niemi, Tarja
Taittonen, Markku
Nuutila, Pirjo
Virtanen, Kirsi A.
Langin, Dominique
Scheideler, Marcel
Amri, Ez-Zoubir
author_facet Giroud, Maude
Karbiener, Michael
Pisani, Didier F.
Ghandour, Rayane A.
Beranger, Guillaume E.
Niemi, Tarja
Taittonen, Markku
Nuutila, Pirjo
Virtanen, Kirsi A.
Langin, Dominique
Scheideler, Marcel
Amri, Ez-Zoubir
author_sort Giroud, Maude
collection PubMed
description In response to cold or β3-adrenoreceptor stimulation brown adipose tissue (BAT) promotes non-shivering thermogenesis, leading to energy dissipation. BAT has long been thought to be absent or scarce in adult humans. The recent discovery of thermogenic brite/beige adipocytes has opened the way to development of novel innovative strategies to combat overweight/obesity and associated diseases. Thus it is of great interest to identify regulatory factors that govern the brite adipogenic program. Here, we carried out global microRNA (miRNA) expression profiling on human adipocytes to identify miRNAs that are regulated upon the conversion from white to brite adipocytes. Among the miRNAs that were differentially expressed, we found that Let-7i-5p was down regulated in brite adipocytes. A detailed analysis of the Let-7i-5p levels showed an inverse expression of UCP1 in murine and human brite adipocytes both in vivo and in vitro. Functional studies with Let-7i-5p mimic in human brite adipocytes in vitro revealed a decrease in the expression of UCP1 and in the oxygen consumption rate. Moreover, the Let-7i-5p mimic when injected into murine sub-cutaneous white adipose tissue inhibited partially β3-adrenergic activation of the browning process. These results suggest that the miRNAs Let-7i-5p participates in the recruitment and the function of brite adipocytes.
format Online
Article
Text
id pubmed-4921928
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-49219282016-06-28 Let-7i-5p represses brite adipocyte function in mice and humans Giroud, Maude Karbiener, Michael Pisani, Didier F. Ghandour, Rayane A. Beranger, Guillaume E. Niemi, Tarja Taittonen, Markku Nuutila, Pirjo Virtanen, Kirsi A. Langin, Dominique Scheideler, Marcel Amri, Ez-Zoubir Sci Rep Article In response to cold or β3-adrenoreceptor stimulation brown adipose tissue (BAT) promotes non-shivering thermogenesis, leading to energy dissipation. BAT has long been thought to be absent or scarce in adult humans. The recent discovery of thermogenic brite/beige adipocytes has opened the way to development of novel innovative strategies to combat overweight/obesity and associated diseases. Thus it is of great interest to identify regulatory factors that govern the brite adipogenic program. Here, we carried out global microRNA (miRNA) expression profiling on human adipocytes to identify miRNAs that are regulated upon the conversion from white to brite adipocytes. Among the miRNAs that were differentially expressed, we found that Let-7i-5p was down regulated in brite adipocytes. A detailed analysis of the Let-7i-5p levels showed an inverse expression of UCP1 in murine and human brite adipocytes both in vivo and in vitro. Functional studies with Let-7i-5p mimic in human brite adipocytes in vitro revealed a decrease in the expression of UCP1 and in the oxygen consumption rate. Moreover, the Let-7i-5p mimic when injected into murine sub-cutaneous white adipose tissue inhibited partially β3-adrenergic activation of the browning process. These results suggest that the miRNAs Let-7i-5p participates in the recruitment and the function of brite adipocytes. Nature Publishing Group 2016-06-27 /pmc/articles/PMC4921928/ /pubmed/27345691 http://dx.doi.org/10.1038/srep28613 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Giroud, Maude
Karbiener, Michael
Pisani, Didier F.
Ghandour, Rayane A.
Beranger, Guillaume E.
Niemi, Tarja
Taittonen, Markku
Nuutila, Pirjo
Virtanen, Kirsi A.
Langin, Dominique
Scheideler, Marcel
Amri, Ez-Zoubir
Let-7i-5p represses brite adipocyte function in mice and humans
title Let-7i-5p represses brite adipocyte function in mice and humans
title_full Let-7i-5p represses brite adipocyte function in mice and humans
title_fullStr Let-7i-5p represses brite adipocyte function in mice and humans
title_full_unstemmed Let-7i-5p represses brite adipocyte function in mice and humans
title_short Let-7i-5p represses brite adipocyte function in mice and humans
title_sort let-7i-5p represses brite adipocyte function in mice and humans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921928/
https://www.ncbi.nlm.nih.gov/pubmed/27345691
http://dx.doi.org/10.1038/srep28613
work_keys_str_mv AT giroudmaude let7i5prepressesbriteadipocytefunctioninmiceandhumans
AT karbienermichael let7i5prepressesbriteadipocytefunctioninmiceandhumans
AT pisanididierf let7i5prepressesbriteadipocytefunctioninmiceandhumans
AT ghandourrayanea let7i5prepressesbriteadipocytefunctioninmiceandhumans
AT berangerguillaumee let7i5prepressesbriteadipocytefunctioninmiceandhumans
AT niemitarja let7i5prepressesbriteadipocytefunctioninmiceandhumans
AT taittonenmarkku let7i5prepressesbriteadipocytefunctioninmiceandhumans
AT nuutilapirjo let7i5prepressesbriteadipocytefunctioninmiceandhumans
AT virtanenkirsia let7i5prepressesbriteadipocytefunctioninmiceandhumans
AT langindominique let7i5prepressesbriteadipocytefunctioninmiceandhumans
AT scheidelermarcel let7i5prepressesbriteadipocytefunctioninmiceandhumans
AT amriezzoubir let7i5prepressesbriteadipocytefunctioninmiceandhumans