Kaushik Susmita, Juste Yves R, Lindenau Kristen, Dong Shuxian, Macho-González Adrián, Santiago-Fernández Olaya, McCabe Mericka, Singh Rajat, Gavathiotis Evripidis, Cuervo Ana Maria
Department of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
Institute for Aging Studies, Albert Einstein College of Medicine, Bronx, NY, USA.
Sci Adv. 2022 Nov 18;8(46):eabq2733. doi: 10.1126/sciadv.abq2733. Epub 2022 Nov 16.
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.
脂肪生成是一个精心编排的多步骤过程,在此过程中前脂肪细胞分化为脂肪细胞。脂肪生成研究最多的方面是其通过大量基因的适时表达和沉默进行的转录调控。然而,关键调节蛋白本身的周转是否控制脂肪生成在很大程度上仍未得到充分研究。伴侣介导的自噬(CMA)是溶酶体蛋白降解的一种选择性形式,它响应各种信号,为调节目的重塑蛋白质组。我们在此报告脂肪细胞分化过程中CMA的激活,并表明CMA通过适时降解关键调节信号蛋白和转录因子来调节脂肪生成的不同步骤,这些蛋白和转录因子决定了脂肪生成所需的增殖、能量适应和信号变化。