Chaperone-mediated autophagy regulates adipocyte differentiation

Author:

Kaushik Susmita12ORCID,Juste Yves R.12ORCID,Lindenau Kristen12ORCID,Dong Shuxian12ORCID,Macho-González Adrián12ORCID,Santiago-Fernández Olaya12ORCID,McCabe Mericka123ORCID,Singh Rajat124ORCID,Gavathiotis Evripidis234ORCID,Cuervo Ana Maria124ORCID

Affiliation:

1. Department of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY, USA.

2. Institute for Aging Studies, Albert Einstein College of Medicine, Bronx, NY, USA.

3. Department of Biochemistry, Albert Einstein College of Medicine, Bronx, NY, USA.

4. Department of Medicine, Albert Einstein College of Medicine, Bronx, NY, USA.

Abstract

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 remains largely understudied. Chaperone-mediated autophagy (CMA) is a selective form of lysosomal protein degradation 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 proliferation, energetic adaptation, and signaling changes required for adipogenesis.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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