期刊论文详细信息
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE 卷:1867
Reduction in endoplasmic reticulum stress activates beige adipocytes differentiation and alleviates high fat diet-induced metabolic phenotypes
Article
Lee, Ji-Min1  Park, Soyoung2  Lee, Duckgue1  Ginting, Rehna Paula2  Lee, Man Ryul1,2  Lee, Min-Woo1,2  Han, Jaeseok1,2 
[1] Soonchunhyang Univ, Soonchunhyang Inst Medibio Sci SIMS, Cheonan Si 31151, Chungcheongnam, South Korea
[2] Soonchunhyang Univ, Dept Integrated Biomed Sci, Cheonan Si 31151, South Korea
关键词: Adipocyte;    Browning;    Endoplasmic reticulum;    C/EBP homologous protein;    TUDCA;    UCP1;   
DOI  :  10.1016/j.bbadis.2021.166099
来源: Elsevier
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【 摘 要 】

Endoplasmic reticulum (ER) stress is closely associated with various metabolic diseases, such as obesity and diabetes. Development of beige/brite adipocytes increases thermogenesis and helps to reduce obesity. Although the relationship between ER stress and white adipocytes has been studied considerably, the possible role of ER stress and the unfolded protein response (UPR) induction in beige adipocytes differentiation remain to be investigated. In this study we investigated how ER stress affected beige adipocytes differentiation both in vitro and in vivo. Phosphorylation of eIF2 alpha was transiently decreased in the early phase (day 2), whereas it was induced at the late phase with concomitant induction of C/EBP homologous protein (CHOP) during beige adipocytes differentiation. Forced expression of CHOP inhibited the expression of beige adipocytes markers, including Ucp1, Cox8b, Cidea, Prdm16, and Pgc-1 alpha, following the induction of beige adipocytes differentiation. When ER stress was reduced by the chemical chaperone tauroursodeoxycholic acid (TUDCA), the expression of the beige adipocytes marker uncoupling protein 1 (UCP1) was significantly enhanced in inguinal white adipose tissue (iWAT) and high fat diet (HFD)-induced abnormal metabolic phenotype was improved. In summary, we found that ER stress and the UPR induction were closely involved in beige adipogenesis. These results suggest that modulating ER stress could be a potential therapeutic intervention against metabolic dysfunctions via activation of iWAT browning.

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