Cargando…
Acute exercise regulates adipogenic gene expression in white adipose tissue
White adipose tissue expansion is associated with both hypertrophy and hyperplasia of adipocytes. Exercise training results in adipocyte hypotrophy by activating lipolysis, but it is poorly understood whether exercise regulates adipogenesis by altering adipogenic gene expression. The purpose of this...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Institute of Sport in Warsaw
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5143777/ https://www.ncbi.nlm.nih.gov/pubmed/28090143 http://dx.doi.org/10.5604/20831862.1224395 |
_version_ | 1782472999274807296 |
---|---|
author | Shen, Y Zhou, H Jin, W Lee, HJ |
author_facet | Shen, Y Zhou, H Jin, W Lee, HJ |
author_sort | Shen, Y |
collection | PubMed |
description | White adipose tissue expansion is associated with both hypertrophy and hyperplasia of adipocytes. Exercise training results in adipocyte hypotrophy by activating lipolysis, but it is poorly understood whether exercise regulates adipogenesis by altering adipogenic gene expression. The purpose of this study was to evaluate the effect of a single bout of swimming exercise on adipogenic gene expression in white adipose tissue (WAT). Male C57BL/6J mice were divided into two groups: a sedentary control group and a 120-minute swimming exercise group. Immediately after acute exercise, adipogenic gene expression in WAT was analysed by RT-PCR, and tdTomato positive cells in WAT from UCP1-cre-tdTomato mice were observed under a confocal microscope. In epididymal white adipose tissue (eWAT), PPARγ2 and C/EBPα expression at the mRNA level was significantly decreased with high induction of Wnt10b and KLFs (KLF2, KLF3, KLF7, KLF6, KLF9 and KLF15), whereas PPARγ2, not C/EBPα, was decreased with high induction of Wnt6 and KLFs (KLF2, KLF3, KLF7, KLF6 and KLF9) in inguinal white adipose tissue (iWAT) after acute exercise. The expression of C/EBPβ and C/EBPδ was upregulated in both WATs with a high level of PGC-1α expression. Expression level of UCP1 was increased only in adipocytes of eWAT, while beige cell specific gene expression was comparable between groups and tdTomato positive cells were not found in WAT of UCP1-cre-tdTomato reporter mouse immediately after acute exercise. These results suggest that acute exercise suppresses adipogenic gene expression and may regulate thermogenesis by activating C/EBPβ, PGC-1α and UCP1 in WAT. |
format | Online Article Text |
id | pubmed-5143777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Institute of Sport in Warsaw |
record_format | MEDLINE/PubMed |
spelling | pubmed-51437772017-01-13 Acute exercise regulates adipogenic gene expression in white adipose tissue Shen, Y Zhou, H Jin, W Lee, HJ Biol Sport Original Paper White adipose tissue expansion is associated with both hypertrophy and hyperplasia of adipocytes. Exercise training results in adipocyte hypotrophy by activating lipolysis, but it is poorly understood whether exercise regulates adipogenesis by altering adipogenic gene expression. The purpose of this study was to evaluate the effect of a single bout of swimming exercise on adipogenic gene expression in white adipose tissue (WAT). Male C57BL/6J mice were divided into two groups: a sedentary control group and a 120-minute swimming exercise group. Immediately after acute exercise, adipogenic gene expression in WAT was analysed by RT-PCR, and tdTomato positive cells in WAT from UCP1-cre-tdTomato mice were observed under a confocal microscope. In epididymal white adipose tissue (eWAT), PPARγ2 and C/EBPα expression at the mRNA level was significantly decreased with high induction of Wnt10b and KLFs (KLF2, KLF3, KLF7, KLF6, KLF9 and KLF15), whereas PPARγ2, not C/EBPα, was decreased with high induction of Wnt6 and KLFs (KLF2, KLF3, KLF7, KLF6 and KLF9) in inguinal white adipose tissue (iWAT) after acute exercise. The expression of C/EBPβ and C/EBPδ was upregulated in both WATs with a high level of PGC-1α expression. Expression level of UCP1 was increased only in adipocytes of eWAT, while beige cell specific gene expression was comparable between groups and tdTomato positive cells were not found in WAT of UCP1-cre-tdTomato reporter mouse immediately after acute exercise. These results suggest that acute exercise suppresses adipogenic gene expression and may regulate thermogenesis by activating C/EBPβ, PGC-1α and UCP1 in WAT. Institute of Sport in Warsaw 2016-11-10 2016-12 /pmc/articles/PMC5143777/ /pubmed/28090143 http://dx.doi.org/10.5604/20831862.1224395 Text en Copyright © Biology of Sport 2016 http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Paper Shen, Y Zhou, H Jin, W Lee, HJ Acute exercise regulates adipogenic gene expression in white adipose tissue |
title | Acute exercise regulates adipogenic gene expression in white adipose tissue |
title_full | Acute exercise regulates adipogenic gene expression in white adipose tissue |
title_fullStr | Acute exercise regulates adipogenic gene expression in white adipose tissue |
title_full_unstemmed | Acute exercise regulates adipogenic gene expression in white adipose tissue |
title_short | Acute exercise regulates adipogenic gene expression in white adipose tissue |
title_sort | acute exercise regulates adipogenic gene expression in white adipose tissue |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5143777/ https://www.ncbi.nlm.nih.gov/pubmed/28090143 http://dx.doi.org/10.5604/20831862.1224395 |
work_keys_str_mv | AT sheny acuteexerciseregulatesadipogenicgeneexpressioninwhiteadiposetissue AT zhouh acuteexerciseregulatesadipogenicgeneexpressioninwhiteadiposetissue AT jinw acuteexerciseregulatesadipogenicgeneexpressioninwhiteadiposetissue AT leehj acuteexerciseregulatesadipogenicgeneexpressioninwhiteadiposetissue |