Cdo1 promotes PPARγ-mediated adipose tissue lipolysis in male mice

被引:46
作者
Guo, Ying-Ying [1 ,2 ]
Li, Bai-Yu [1 ,2 ]
Xiao, Gang [1 ,2 ]
Liu, Yang [1 ,2 ]
Guo, Liang [3 ,4 ]
Tang, Qi-Qun [1 ,2 ]
机构
[1] Fudan Univ, Key Lab Metab & Mol Med, Sch Basic Med Sci, Dept Biochem & Mol Biol,Minist Educ, Shanghai, Peoples R China
[2] Fudan Univ, Dept Endocrinol & Metab, Zhongshan Hosp, Shanghai, Peoples R China
[3] Shanghai Univ Sport, Shanghai Frontiers Sci Res Base Exercise & Metab, Shanghai, Peoples R China
[4] Shanghai Univ Sport, Sch Kinesiol, Shanghai, Peoples R China
基金
国家重点研发计划;
关键词
ACTIVATED RECEPTOR-GAMMA; CYSTEINE DIOXYGENASE; TRIGLYCERIDE LIPASE; IN-VIVO; BROWN; ALPHA; GENE; ADIPOGENESIS; ADIPOCYTES; METABOLISM;
D O I
10.1038/s42255-022-00644-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Guo et al. show that Cdo1, a taurine-synthesis enzyme, interacts with PPAR gamma to promote its transactivation of genes encoding the lipases ATGL and HSL, thereby promoting adipose tissue lipolysis and ameliorating diet-induced obesity. Cysteine dioxygenase 1 (Cdo1) is a key enzyme in taurine synthesis. Here we show that Cdo1 promotes lipolysis in adipose tissue. Adipose-specific knockout of Cdo1 in mice impairs energy expenditure, cold tolerance and lipolysis, exacerbates diet-induced obesity (DIO) and decreases adipose expression of the key lipolytic genes encoding ATGL and HSL, with little effect on adipose taurine levels. White-adipose-specific overexpression of ATGL and HSL blunts the role of adipose Cdo1 deficiency in promoting DIO. Mechanistically, Cdo1 interacts with PPAR gamma and facilitates the recruitment of Med24, the core subunit of mediator complex, to ATGL and HSL gene promoters, thereby transactivating their expression. Further, mice with transgenic overexpression of Cdo1 show better cold tolerance, ameliorated DIO and higher lipolysis capacity. Thus, we uncover an unexpected and important role of Cdo1 in regulating adipose lipolysis.
引用
收藏
页码:1352 / +
页数:35
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