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Direct conversion of human fibroblasts to brown adipocytes by small chemical compounds
Brown adipocytes play an important role in human energy metabolism and prevention of obesity and diabetes. Induced pluripotent stem cells (iPSCs) represent a promising source for brown adipocytes; however, exogenous gene induction is generally required for iPSCs generation, which might cause undesir...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487346/ https://www.ncbi.nlm.nih.gov/pubmed/28655922 http://dx.doi.org/10.1038/s41598-017-04665-x |
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author | Takeda, Yukimasa Harada, Yoshinori Yoshikawa, Toshikazu Dai, Ping |
author_facet | Takeda, Yukimasa Harada, Yoshinori Yoshikawa, Toshikazu Dai, Ping |
author_sort | Takeda, Yukimasa |
collection | PubMed |
description | Brown adipocytes play an important role in human energy metabolism and prevention of obesity and diabetes. Induced pluripotent stem cells (iPSCs) represent a promising source for brown adipocytes; however, exogenous gene induction is generally required for iPSCs generation, which might cause undesired effects particularly in long-term treatment after transplantation. We have previously reported a cocktail of six small chemical compounds that enables a conversion of human fibroblasts into chemical compound-induced neuronal cells (CiNCs). Here, we report that modified combinations of the chemical compounds and rosiglitazone, a PPARγ agonist, afforded direct conversion of human fibroblasts into brown adipocytes. The chemical compound-induced brown adipocytes (ciBAs) exhibit induction of human brown adipocyte-specific genes such as Ucp1, Ckmt1, Cited1 and other adipocyte-specific genes such as Fabp4, AdipoQ, and Pparγ. Treatment with either isoproterenol or Forskolin further induced the expression of Ucp1, suggesting that β adrenergic receptor signalling in ciBAs could be functional for induction of thermogenic genes. Moreover, oxygen consumption rates were elevated in ciBAs along with increase of cellular mitochondria. Our findings might provide an easily accessible approach for generating human brown adipocytes from fibroblasts and offer therapeutic potential for the management of obesity, diabetes, and related metabolic disorders. |
format | Online Article Text |
id | pubmed-5487346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54873462017-06-30 Direct conversion of human fibroblasts to brown adipocytes by small chemical compounds Takeda, Yukimasa Harada, Yoshinori Yoshikawa, Toshikazu Dai, Ping Sci Rep Article Brown adipocytes play an important role in human energy metabolism and prevention of obesity and diabetes. Induced pluripotent stem cells (iPSCs) represent a promising source for brown adipocytes; however, exogenous gene induction is generally required for iPSCs generation, which might cause undesired effects particularly in long-term treatment after transplantation. We have previously reported a cocktail of six small chemical compounds that enables a conversion of human fibroblasts into chemical compound-induced neuronal cells (CiNCs). Here, we report that modified combinations of the chemical compounds and rosiglitazone, a PPARγ agonist, afforded direct conversion of human fibroblasts into brown adipocytes. The chemical compound-induced brown adipocytes (ciBAs) exhibit induction of human brown adipocyte-specific genes such as Ucp1, Ckmt1, Cited1 and other adipocyte-specific genes such as Fabp4, AdipoQ, and Pparγ. Treatment with either isoproterenol or Forskolin further induced the expression of Ucp1, suggesting that β adrenergic receptor signalling in ciBAs could be functional for induction of thermogenic genes. Moreover, oxygen consumption rates were elevated in ciBAs along with increase of cellular mitochondria. Our findings might provide an easily accessible approach for generating human brown adipocytes from fibroblasts and offer therapeutic potential for the management of obesity, diabetes, and related metabolic disorders. Nature Publishing Group UK 2017-06-27 /pmc/articles/PMC5487346/ /pubmed/28655922 http://dx.doi.org/10.1038/s41598-017-04665-x Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Takeda, Yukimasa Harada, Yoshinori Yoshikawa, Toshikazu Dai, Ping Direct conversion of human fibroblasts to brown adipocytes by small chemical compounds |
title | Direct conversion of human fibroblasts to brown adipocytes by small chemical compounds |
title_full | Direct conversion of human fibroblasts to brown adipocytes by small chemical compounds |
title_fullStr | Direct conversion of human fibroblasts to brown adipocytes by small chemical compounds |
title_full_unstemmed | Direct conversion of human fibroblasts to brown adipocytes by small chemical compounds |
title_short | Direct conversion of human fibroblasts to brown adipocytes by small chemical compounds |
title_sort | direct conversion of human fibroblasts to brown adipocytes by small chemical compounds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487346/ https://www.ncbi.nlm.nih.gov/pubmed/28655922 http://dx.doi.org/10.1038/s41598-017-04665-x |
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