3-tert-Butyl-4-hydroxyanisole Perturbs Differentiation of C3H10T1/2 Mesenchymal Stem Cells into Brown Adipocytes through Regulating Smad Signaling

被引:5
|
作者
Wang, Xiaoyun [1 ,2 ]
Sun, Zhendong [3 ]
Pei, Yao [1 ,2 ]
Liu, Qian S. [1 ]
Zhou, Qunfang [1 ,2 ,3 ]
Jiang, Guibin [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Res Ctr Ecoenvironm Sci, State Key Lab Environm Chem & Ecotoxicol, Beijing 100085, Peoples R China
[2] Univ Chinese Acad Sci, Coll Resources & Environm, Beijing 100049, Peoples R China
[3] Univ Chinese Acad Sci, Hangzhou Inst Adv Study, Sch Environm, Hangzhou 310024, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
3-tert-butyl-4-hydroxyanisole; 2mesenchymal stem cells; adipogenic differentiation; thermogenic capacity; Smad signaling; SYNTHETIC PHENOLIC ANTIOXIDANTS; BISPHENOL-A; IN-VITRO; FAT; METABOLITES; COMMITMENT; OBESITY; WHITE;
D O I
10.1021/acs.est.3c02346
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Exposure to 3-BHA induced a shift from a brown to white-likephenotype in C3H10T1/2 mesenchymal stem cells by promoting the phosphorylationof Smad1/5/8. 3-tert-Butyl-4-hydroxyanisole (3-BHA),one ofthe most commonly used antioxidants in foodstuffs, has been identifiedas an environmental endocrine disruptor (EED) with obesogenic activity.Given the increasing concern on EED-caused dysfunction in lipid metabolism,whether 3-BHA could influence the development of brown adipocytesis worthy of being explored. In this study, the effect of 3-BHA onthe differentiation of C3H10T1/2 mesenchymal stem cells (MSCs) intobrown adipocytes was investigated. Exposure to 3-BHA promoted lipogenesisof the differentiated cells, as evidenced by the increased intracellularlipid accumulation and elevated expressions of adipogenic biomarkers,including peroxisome proliferator-activated receptor & gamma; (PPAR & gamma;), Perilipin, Adiponectin, and fatty acid binding protein 4 (FABP4). Surprisingly,the thermogenic capacity of the differentiated cells was compromisedas a result of 3-BHA exposure, because neither intracellular mitochondrialcontents nor expressions of thermogenic biomarkers, including uncouplingprotein 1 (UCP1), peroxisome proliferator-activatedreceptor & gamma; coactivator 1 & alpha; (PGC1 & alpha;), cell-death-inducing DNA fragmentation factor & alpha; subunit-likeeffector A (CIDEA), and PR domain containing 16 (PRDM16), were increased by this chemical. The underlyingmolecular mechanism exploration revealed that, in contrast to p38MAPK, 3-BHA stimulation induced phosphorylation of Smad1/5/8 in anexposure time-dependent manner, suggesting that this chemical-triggeredSmad signaling was responsible for the shift of C3H10T1/2 MSC differentiationfrom a brown to white-like phenotype. The finding herein, for thefirst time, revealed the perturbation of 3-BHA in the developmentof brown adipocytes, uncovering new knowledge about the obesogenicpotential of this emerging chemical of concern.
引用
收藏
页码:10998 / 11008
页数:11
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