{"title":"GPR180 Reduces Adiposity by Inhibiting Lipogenesis and Fatty Acid Uptake in Adipocytes.","authors":"Ziming Zhu, Yaxu Yang, Lijun Sun, Yunhua Zhang, Xue Han, Chao Luo, Yue Yin, Weizhen Zhang","doi":"10.1152/ajpendo.00178.2024","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objective:</b> In this study, we examined the effect of Gpr180, a G protein-coupled receptor (GPCR) family member, on lipid metabolism of adipose tissue. <b>Methods:</b> We utilized adeno-associated virus overexpression of <i>Gpr180</i> in subcutaneous adipose tissue, adipocyte-specific <i>Gpr180</i> knockout mice and stromal vascular fraction (SVF) cells to explore the role and mechanism of GPR180 in lipid metabolism in adipocytes. <b>Results:</b> Levels of <i>Gpr180</i> mRNA in subcutaneous and epididymal adipose tissues were significantly reduced in mice fed high fat diet (HFD). Over-expression of <i>Gpr180</i> in subcutaneous white adipose tissue (sWAT) improved lipid metabolism and protected mice from HFD-induced obesity. Conversely, adipocyte-specific knockout of <i>Gpr180</i> exacerbated lipid metabolism disorders induced by HFD. In cultured adipocytes differentiated from SVF cells, GPR180 inhibited lipogenesis and fatty acid (FA) uptake. <b>Conclusions:</b> Collectively, our study reveals that GPR180 functions to suppress lipid accumulation in adipocytes.</p>","PeriodicalId":7594,"journal":{"name":"American journal of physiology. Endocrinology and metabolism","volume":" ","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of physiology. Endocrinology and metabolism","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1152/ajpendo.00178.2024","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: In this study, we examined the effect of Gpr180, a G protein-coupled receptor (GPCR) family member, on lipid metabolism of adipose tissue. Methods: We utilized adeno-associated virus overexpression of Gpr180 in subcutaneous adipose tissue, adipocyte-specific Gpr180 knockout mice and stromal vascular fraction (SVF) cells to explore the role and mechanism of GPR180 in lipid metabolism in adipocytes. Results: Levels of Gpr180 mRNA in subcutaneous and epididymal adipose tissues were significantly reduced in mice fed high fat diet (HFD). Over-expression of Gpr180 in subcutaneous white adipose tissue (sWAT) improved lipid metabolism and protected mice from HFD-induced obesity. Conversely, adipocyte-specific knockout of Gpr180 exacerbated lipid metabolism disorders induced by HFD. In cultured adipocytes differentiated from SVF cells, GPR180 inhibited lipogenesis and fatty acid (FA) uptake. Conclusions: Collectively, our study reveals that GPR180 functions to suppress lipid accumulation in adipocytes.
期刊介绍:
The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.