Chaperone-mediated autophagy regulates adipocyte differentiation.
Susmita KaushikYves R JusteKristen L LindenauShuxian DongAdrián Macho-GonzálezOlaya Santiago-FernándezMericka McCabeRajat SinghEvripidis GavathiotisAna Maria CuervoPublished in: Science advances (2022)
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.
Keyphrases
- transcription factor
- high fat diet induced
- insulin resistance
- adipose tissue
- signaling pathway
- cell death
- endoplasmic reticulum stress
- oxidative stress
- fatty acid
- genome wide identification
- type diabetes
- binding protein
- genome wide
- bone mineral density
- dna methylation
- endoplasmic reticulum
- body composition
- amino acid
- postmenopausal women