GLP-1/GLP-1R Signaling in Regulation of Adipocyte Differentiation and Lipogenesis

Background/Aims: The aim of this study was to determine the direct role of liraglutide (LG) in adipogenesis and lipid metabolism. Methods: Lipid accumulation was evaluated by oil red O staining, quantitative real-time PCR (qPCR) was performed to determine glucagon-like peptide 1 receptor (GLP-1R), f...

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Main Authors: Jicui Chen, Huichen Zhao, Xiaoli Ma, Yuchao Zhang, Sumei Lu, Yangang Wang, Chen Zong, Dandan Qin, Yuanmei Wang, Yingfeng Yingfeng Yang, Xiangdong Wang, Yuantao Liu
Format: Article
Language:English
Published: Cell Physiol Biochem Press GmbH & Co KG 2017-06-01
Series:Cellular Physiology and Biochemistry
Subjects:
Online Access:http://www.karger.com/Article/FullText/478872
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author Jicui Chen
Huichen Zhao
Xiaoli Ma
Yuchao Zhang
Sumei Lu
Yangang Wang
Chen Zong
Dandan Qin
Yuanmei Wang
Yingfeng Yingfeng Yang
Xiangdong Wang
Yuantao Liu
author_facet Jicui Chen
Huichen Zhao
Xiaoli Ma
Yuchao Zhang
Sumei Lu
Yangang Wang
Chen Zong
Dandan Qin
Yuanmei Wang
Yingfeng Yingfeng Yang
Xiangdong Wang
Yuantao Liu
author_sort Jicui Chen
collection DOAJ
description Background/Aims: The aim of this study was to determine the direct role of liraglutide (LG) in adipogenesis and lipid metabolism. Methods: Lipid accumulation was evaluated by oil red O staining, quantitative real-time PCR (qPCR) was performed to determine glucagon-like peptide 1 receptor (GLP-1R), fatty acid synthase (FASN) and adipose triglyceride lipase (ATGL) expression in 3T3-L1 preadipocytes, differentiated adipocytes and in adipose tissues from mice. The effects of LG on 3T3-L1 adipogenesis and lipid metabolism were analyzed with qPCR, Western Blotting, oil red O staining, immunohistochemistry (IHC) and immunofluorescence (IF). All measurements were performed at least three times. Results: LG increased the expression of differentiation marker genes and lipid accumulation during preadipocyte differentiation. In differentiated adipocytes, LG decreased FASN expression, and simultaneously led to CREB phosphorylation and ERK1/2 activation which were abolished by a GLP-1R antagonist, exendin (9-39). LG induced-FASN down-regulation was partially reversed by PKA and ERK1/2 inhibitors. Consistent with above in vitro findings, LG treatment significantly reduced FASN expression in visceral adipose tissues of ob/ob mice, and reduced body weight gain. Conclusion: LG promotes preadipocytes differentiation, and inhibits FASN expression in adipocytes. LG induced down-regulation of FASN is at least partially mediated by PKA and MAPK signaling pathways.
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spelling doaj.art-3e7f343fdf564be3bff25449c0392eff2022-12-21T18:54:14ZengCell Physiol Biochem Press GmbH & Co KGCellular Physiology and Biochemistry1015-89871421-97782017-06-014231165117610.1159/000478872478872GLP-1/GLP-1R Signaling in Regulation of Adipocyte Differentiation and LipogenesisJicui ChenHuichen ZhaoXiaoli MaYuchao ZhangSumei LuYangang WangChen ZongDandan QinYuanmei WangYingfeng Yingfeng YangXiangdong WangYuantao LiuBackground/Aims: The aim of this study was to determine the direct role of liraglutide (LG) in adipogenesis and lipid metabolism. Methods: Lipid accumulation was evaluated by oil red O staining, quantitative real-time PCR (qPCR) was performed to determine glucagon-like peptide 1 receptor (GLP-1R), fatty acid synthase (FASN) and adipose triglyceride lipase (ATGL) expression in 3T3-L1 preadipocytes, differentiated adipocytes and in adipose tissues from mice. The effects of LG on 3T3-L1 adipogenesis and lipid metabolism were analyzed with qPCR, Western Blotting, oil red O staining, immunohistochemistry (IHC) and immunofluorescence (IF). All measurements were performed at least three times. Results: LG increased the expression of differentiation marker genes and lipid accumulation during preadipocyte differentiation. In differentiated adipocytes, LG decreased FASN expression, and simultaneously led to CREB phosphorylation and ERK1/2 activation which were abolished by a GLP-1R antagonist, exendin (9-39). LG induced-FASN down-regulation was partially reversed by PKA and ERK1/2 inhibitors. Consistent with above in vitro findings, LG treatment significantly reduced FASN expression in visceral adipose tissues of ob/ob mice, and reduced body weight gain. Conclusion: LG promotes preadipocytes differentiation, and inhibits FASN expression in adipocytes. LG induced down-regulation of FASN is at least partially mediated by PKA and MAPK signaling pathways.http://www.karger.com/Article/FullText/478872Liraglutide3T3-L1 preadipocytesAdipogenesisFASN
spellingShingle Jicui Chen
Huichen Zhao
Xiaoli Ma
Yuchao Zhang
Sumei Lu
Yangang Wang
Chen Zong
Dandan Qin
Yuanmei Wang
Yingfeng Yingfeng Yang
Xiangdong Wang
Yuantao Liu
GLP-1/GLP-1R Signaling in Regulation of Adipocyte Differentiation and Lipogenesis
Cellular Physiology and Biochemistry
Liraglutide
3T3-L1 preadipocytes
Adipogenesis
FASN
title GLP-1/GLP-1R Signaling in Regulation of Adipocyte Differentiation and Lipogenesis
title_full GLP-1/GLP-1R Signaling in Regulation of Adipocyte Differentiation and Lipogenesis
title_fullStr GLP-1/GLP-1R Signaling in Regulation of Adipocyte Differentiation and Lipogenesis
title_full_unstemmed GLP-1/GLP-1R Signaling in Regulation of Adipocyte Differentiation and Lipogenesis
title_short GLP-1/GLP-1R Signaling in Regulation of Adipocyte Differentiation and Lipogenesis
title_sort glp 1 glp 1r signaling in regulation of adipocyte differentiation and lipogenesis
topic Liraglutide
3T3-L1 preadipocytes
Adipogenesis
FASN
url http://www.karger.com/Article/FullText/478872
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