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MicroRNAs Are Required for the Feature Maintenance and Differentiation of Brown Adipocytes
Brown adipose tissue (BAT) is specialized to burn lipids for heat generation as a natural defense against cold and obesity. Previous studies established microRNAs (miRNAs) as essential regulators of brown adipocyte differentiation, but whether miRNAs are required for the feature maintenance of matur...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238002/ https://www.ncbi.nlm.nih.gov/pubmed/25008181 http://dx.doi.org/10.2337/db14-0466 |
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author | Kim, Hye-Jin Cho, Hyunjii Alexander, Ryan Patterson, Heide Christine Gu, Minxia Lo, Kinyui Alice Xu, Dan Goh, Vera J. Nguyen, Long N. Chai, Xiaoran Huang, Cher X. Kovalik, Jean-Paul Ghosh, Sujoy Trajkovski, Mirko Silver, David L. Lodish, Harvey Sun, Lei |
author_facet | Kim, Hye-Jin Cho, Hyunjii Alexander, Ryan Patterson, Heide Christine Gu, Minxia Lo, Kinyui Alice Xu, Dan Goh, Vera J. Nguyen, Long N. Chai, Xiaoran Huang, Cher X. Kovalik, Jean-Paul Ghosh, Sujoy Trajkovski, Mirko Silver, David L. Lodish, Harvey Sun, Lei |
author_sort | Kim, Hye-Jin |
collection | PubMed |
description | Brown adipose tissue (BAT) is specialized to burn lipids for heat generation as a natural defense against cold and obesity. Previous studies established microRNAs (miRNAs) as essential regulators of brown adipocyte differentiation, but whether miRNAs are required for the feature maintenance of mature brown adipocytes remains unknown. To address this question, we ablated Dgcr8, a key regulator of the miRNA biogenesis pathway, in mature brown as well as in white adipocytes. Adipose tissue–specific Dgcr8 knockout mice displayed enlarged but pale interscapular brown fat with decreased expression of genes characteristic of brown fat and were intolerant to cold exposure. Primary brown adipocyte cultures in vitro confirmed that miRNAs are required for marker gene expression in mature brown adipocytes. We also demonstrated that miRNAs are essential for the browning of subcutaneous white adipocytes in vitro and in vivo. Using this animal model, we performed miRNA expression profiling analysis and identified a set of BAT-specific miRNAs that are upregulated during brown adipocyte differentiation and enriched in brown fat compared with other organs. We identified miR-182 and miR-203 as new regulators of brown adipocyte development. Taken together, our study demonstrates an essential role of miRNAs in the maintenance as well as in the differentiation of brown adipocytes. |
format | Online Article Text |
id | pubmed-4238002 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-42380022015-12-01 MicroRNAs Are Required for the Feature Maintenance and Differentiation of Brown Adipocytes Kim, Hye-Jin Cho, Hyunjii Alexander, Ryan Patterson, Heide Christine Gu, Minxia Lo, Kinyui Alice Xu, Dan Goh, Vera J. Nguyen, Long N. Chai, Xiaoran Huang, Cher X. Kovalik, Jean-Paul Ghosh, Sujoy Trajkovski, Mirko Silver, David L. Lodish, Harvey Sun, Lei Diabetes Metabolism Brown adipose tissue (BAT) is specialized to burn lipids for heat generation as a natural defense against cold and obesity. Previous studies established microRNAs (miRNAs) as essential regulators of brown adipocyte differentiation, but whether miRNAs are required for the feature maintenance of mature brown adipocytes remains unknown. To address this question, we ablated Dgcr8, a key regulator of the miRNA biogenesis pathway, in mature brown as well as in white adipocytes. Adipose tissue–specific Dgcr8 knockout mice displayed enlarged but pale interscapular brown fat with decreased expression of genes characteristic of brown fat and were intolerant to cold exposure. Primary brown adipocyte cultures in vitro confirmed that miRNAs are required for marker gene expression in mature brown adipocytes. We also demonstrated that miRNAs are essential for the browning of subcutaneous white adipocytes in vitro and in vivo. Using this animal model, we performed miRNA expression profiling analysis and identified a set of BAT-specific miRNAs that are upregulated during brown adipocyte differentiation and enriched in brown fat compared with other organs. We identified miR-182 and miR-203 as new regulators of brown adipocyte development. Taken together, our study demonstrates an essential role of miRNAs in the maintenance as well as in the differentiation of brown adipocytes. American Diabetes Association 2014-12 2014-11-13 /pmc/articles/PMC4238002/ /pubmed/25008181 http://dx.doi.org/10.2337/db14-0466 Text en © 2014 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. |
spellingShingle | Metabolism Kim, Hye-Jin Cho, Hyunjii Alexander, Ryan Patterson, Heide Christine Gu, Minxia Lo, Kinyui Alice Xu, Dan Goh, Vera J. Nguyen, Long N. Chai, Xiaoran Huang, Cher X. Kovalik, Jean-Paul Ghosh, Sujoy Trajkovski, Mirko Silver, David L. Lodish, Harvey Sun, Lei MicroRNAs Are Required for the Feature Maintenance and Differentiation of Brown Adipocytes |
title | MicroRNAs Are Required for the Feature Maintenance and Differentiation of Brown Adipocytes |
title_full | MicroRNAs Are Required for the Feature Maintenance and Differentiation of Brown Adipocytes |
title_fullStr | MicroRNAs Are Required for the Feature Maintenance and Differentiation of Brown Adipocytes |
title_full_unstemmed | MicroRNAs Are Required for the Feature Maintenance and Differentiation of Brown Adipocytes |
title_short | MicroRNAs Are Required for the Feature Maintenance and Differentiation of Brown Adipocytes |
title_sort | micrornas are required for the feature maintenance and differentiation of brown adipocytes |
topic | Metabolism |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238002/ https://www.ncbi.nlm.nih.gov/pubmed/25008181 http://dx.doi.org/10.2337/db14-0466 |
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