Cargando…
TSH promotes adiposity by inhibiting the browning of white fat
Adiposity is caused by an imbalance between energy intake and consumption. Promotion of the browning of white fat increases energy expenditure and could combat adiposity. Thyroid-stimulating hormone (TSH) has been confirmed to positively correlate with adiposity. However, the putative connection bet...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469524/ https://www.ncbi.nlm.nih.gov/pubmed/32579056 http://dx.doi.org/10.1080/21623945.2020.1783101 |
_version_ | 1783578433499955200 |
---|---|
author | Zhang, Jianmei Wu, Huixiao Ma, Shizhan Gao, Ling Yu, Chunxiao Jing, Fei Zhao, Jiajun |
author_facet | Zhang, Jianmei Wu, Huixiao Ma, Shizhan Gao, Ling Yu, Chunxiao Jing, Fei Zhao, Jiajun |
author_sort | Zhang, Jianmei |
collection | PubMed |
description | Adiposity is caused by an imbalance between energy intake and consumption. Promotion of the browning of white fat increases energy expenditure and could combat adiposity. Thyroid-stimulating hormone (TSH) has been confirmed to positively correlate with adiposity. However, the putative connection between TSH and white adipose browning has never been explored. In this study, we sought to assess the effect of TSH on white adipose tissue browning and energy metabolism. Subclinical hypothyroidism mice, thyroid-specific Tshr-knockout mice injected with TSH, adipocyte-specific and global Tshr-knockout micewere subjected to morphological, physiological, genetic or protein expression analyses and metabolic cages to determine the role of TSH on the browning of white adipose tissue and metabolism. 3T3-L1 and primary SVF cells were used to verify the effects and mechanism of TSH on the browning of white adipocytes. We show that increased circulation TSH level decreases energy expenditure, promotes adiposity, impairs glucose and lipid metabolism. Knockout of Tshr decreases adiposity, increases energy expenditureand markedly promotes the development of beige adipocytesin both epididymal and inguinal subcutaneous white fat via a mechanism that likely involves AMPK/PRDM16/PGC1α. Our results reveal an important role of TSH in regulating energy balance and adiposity by inhibiting the browning of white fat. |
format | Online Article Text |
id | pubmed-7469524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-74695242020-09-15 TSH promotes adiposity by inhibiting the browning of white fat Zhang, Jianmei Wu, Huixiao Ma, Shizhan Gao, Ling Yu, Chunxiao Jing, Fei Zhao, Jiajun Adipocyte Research Article Adiposity is caused by an imbalance between energy intake and consumption. Promotion of the browning of white fat increases energy expenditure and could combat adiposity. Thyroid-stimulating hormone (TSH) has been confirmed to positively correlate with adiposity. However, the putative connection between TSH and white adipose browning has never been explored. In this study, we sought to assess the effect of TSH on white adipose tissue browning and energy metabolism. Subclinical hypothyroidism mice, thyroid-specific Tshr-knockout mice injected with TSH, adipocyte-specific and global Tshr-knockout micewere subjected to morphological, physiological, genetic or protein expression analyses and metabolic cages to determine the role of TSH on the browning of white adipose tissue and metabolism. 3T3-L1 and primary SVF cells were used to verify the effects and mechanism of TSH on the browning of white adipocytes. We show that increased circulation TSH level decreases energy expenditure, promotes adiposity, impairs glucose and lipid metabolism. Knockout of Tshr decreases adiposity, increases energy expenditureand markedly promotes the development of beige adipocytesin both epididymal and inguinal subcutaneous white fat via a mechanism that likely involves AMPK/PRDM16/PGC1α. Our results reveal an important role of TSH in regulating energy balance and adiposity by inhibiting the browning of white fat. Taylor & Francis 2020-06-24 /pmc/articles/PMC7469524/ /pubmed/32579056 http://dx.doi.org/10.1080/21623945.2020.1783101 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zhang, Jianmei Wu, Huixiao Ma, Shizhan Gao, Ling Yu, Chunxiao Jing, Fei Zhao, Jiajun TSH promotes adiposity by inhibiting the browning of white fat |
title | TSH promotes adiposity by inhibiting the browning of white fat |
title_full | TSH promotes adiposity by inhibiting the browning of white fat |
title_fullStr | TSH promotes adiposity by inhibiting the browning of white fat |
title_full_unstemmed | TSH promotes adiposity by inhibiting the browning of white fat |
title_short | TSH promotes adiposity by inhibiting the browning of white fat |
title_sort | tsh promotes adiposity by inhibiting the browning of white fat |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469524/ https://www.ncbi.nlm.nih.gov/pubmed/32579056 http://dx.doi.org/10.1080/21623945.2020.1783101 |
work_keys_str_mv | AT zhangjianmei tshpromotesadipositybyinhibitingthebrowningofwhitefat AT wuhuixiao tshpromotesadipositybyinhibitingthebrowningofwhitefat AT mashizhan tshpromotesadipositybyinhibitingthebrowningofwhitefat AT gaoling tshpromotesadipositybyinhibitingthebrowningofwhitefat AT yuchunxiao tshpromotesadipositybyinhibitingthebrowningofwhitefat AT jingfei tshpromotesadipositybyinhibitingthebrowningofwhitefat AT zhaojiajun tshpromotesadipositybyinhibitingthebrowningofwhitefat |