Chaperone-mediated autophagy regulates adipocyte differentiation

被引:17
|
作者
Kaushik, Susmita [1 ,2 ]
Juste, Yves R. [1 ,2 ]
Lindenau, Kristen [1 ,2 ]
Dong, Shuxian [1 ,2 ]
Macho-Gonzalez, Adrian [1 ,2 ]
Santiago-Fernandez, Olaya [1 ,2 ]
McCabe, Mericka [1 ,2 ,3 ]
Singh, Rajat [1 ,2 ,4 ]
Gavathiotis, Evripidis [2 ,3 ,4 ]
Cuervo, Ana Maria [1 ,2 ,4 ]
机构
[1] Albert Einstein Coll Med, Dept Dev & Mol Biol, Bronx, NY 10467 USA
[2] Albert Einstein Coll Med, Inst Aging Studies, Bronx, NY 10467 USA
[3] Albert Einstein Coll Med, Dept Biochem, Bronx, NY 10467 USA
[4] Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
基金
美国国家卫生研究院;
关键词
UBIQUITIN LIGASE; SELECTIVE UPTAKE; DEGRADATION; ADIPOGENESIS; RECEPTOR; CELL; ACTIVATION; PROTEINS; BLOCKAGE; REVEALS;
D O I
10.1126/sciadv.abq2733
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Adipogenesis is a tightly orchestrated multistep process wherein preadipocytes differentiate into adipocytes. The most studied aspect of adipogenesis is its transcriptional regulation through timely expression and silencing of a vast number of genes. However, whether turnover of key regulatory proteins per se controls adipogenesis re-mains largely understudied. Chaperone-mediated autophagy (CMA) is a selective form of lysosomal protein deg-radation that, in response to diverse cues, remodels the proteome for regulatory purposes. We report here the activation of CMA during adipocyte differentiation and show that CMA regulates adipogenesis at different steps through timely degradation of key regulatory signaling proteins and transcription factors that dictate prolifera-tion, energetic adaptation, and signaling changes required for adipogenesis.
引用
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页数:15
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