ChREBP-β regulates thermogenesis in brown adipose tissue. Issue 3 (June 2020)

• Record Type: Journal Article
• Authors: Wei, Chunchun; Ma, Xianhua; Su, Kai; Qi, Shasha; Zhu, Yuangang; Lin, Junjian; Wang, Chenxin; Yang, Rui; Chen, Xiaowei; Wang, Weizhong; Zhang, Weiping J
• Is Part Of: Journal of endocrinology. Volume 245:Issue 3(2020)
• Page Start: 343
• Page End: 356
• Publication Date: 2020-06
• Subjects: obesity -- lipogenesis -- metabolism -- gene targeting -- transcription factor; Endocrinology -- Periodicals; 616.4005
• DOI: 10.1530/JOE-19-0498
• Languages: English
• ISSNs: 0022-0795

Abstract

Abstract : Brown adipose tissue (BAT) plays a critical role in energy expenditure by uncoupling protein 1 (UCP1)-mediated thermogenesis. Carbohydrate response element-binding protein (ChREBP) is one of the key transcription factors regulating de novo lipogenesis (DNL). As a constitutively active form, ChREBP-β is expressed at extremely low levels. Up to date, its functional relevance in BAT remains unclear. In this study, we show that ChREBP-β inhibits BAT thermogenesis. BAT ChREBP-β mRNA levels were elevated upon cold exposure, which prompted us to generate a mouse model overexpressing ChREBP-β specifically in BAT using the Cre/LoxP approach. ChREBP-β overexpression led to a whitening phenotype of BAT at room temperature, as evidenced by increased lipid droplet size and decreased mitochondrion content. Moreover, BAT thermogenesis was inhibited upon acute cold exposure, and its metabolic remodeling induced by long-term cold adaptation was significantly impaired by ChREBP-β overexpression. Mechanistically, ChREBP-β overexpression downregulated expression of genes involved in mitochondrial biogenesis, autophagy, and respiration. Furthermore, thermogenic gene expression (e.g. Dio2, UCP1) was markedly inhibited in BAT by the overexpressed ChREBP-β. Put together, our work points to ChREBP-β as a negative regulator of thermogenesis in brown adipocytes.