Department of Developmental and Molecular Biology, Marion Bessin Liver Research Center, Institute for Aging Research, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Semin Cell Dev Biol. 2010 Sep;21(7):719-26. doi: 10.1016/j.semcdb.2010.02.005. Epub 2010 Feb 20.
Chaperone-mediated autophagy (CMA) is a selective lysosomal pathway for the degradation of cytosolic proteins. We review in this work some of the recent findings on this pathway regarding the molecular mechanisms that contribute to substrate targeting, binding and translocation across the lysosomal membrane. We have placed particular emphasis on the critical role that changes in the lipid composition of the lysosomal membrane play in the regulation of CMA, as well as the modulatory effect of other novel CMA components. In the second part of this review, we describe the physiological relevance of CMA and its role as one of the cellular mechanisms involved in the response to stress. Changes with age in CMA activity and the contribution of failure of CMA to the phenotype of aging and to the pathogenesis of several age-related pathologies are also described.
伴侣蛋白介导的自噬(CMA)是一种用于降解细胞质蛋白的选择性溶酶体途径。在这项工作中,我们综述了该途径的一些最新发现,包括对底物靶向、结合和穿过溶酶体膜转运的分子机制的研究。我们特别强调了溶酶体膜脂质组成的变化在 CMA 调节中的关键作用,以及其他新型 CMA 成分的调节作用。在本综述的第二部分,我们描述了 CMA 的生理相关性及其作为参与应激反应的细胞机制之一的作用。我们还描述了 CMA 活性随年龄的变化,以及 CMA 功能障碍对衰老表型和几种与年龄相关疾病发病机制的贡献。