Tasset Inmaculada, Cuervo Ana Maria
Department of Developmental and Molecular Biology, Institute for Aging Studies, Albert Einstein College of Medicine, Bronx, NY, USA.
FEBS J. 2016 Jul;283(13):2403-13. doi: 10.1111/febs.13677. Epub 2016 Feb 27.
Different types of autophagy coexist in most mammalian cells, and each of them fulfills very specific tasks in intracellular degradation. Some of these autophagic pathways contribute to cellular metabolism by directly hydrolyzing intracellular lipid stores and glycogen. Chaperone-mediated autophagy (CMA), in contrast, is a selective form of autophagy that can only target proteins for lysosomal degradation. Consequently, it was expected that the only possible contribution of this pathway to cellular metabolism would be by providing free amino acids resulting from protein breakdown. However, recent studies have demonstrated that disturbance in CMA leads to important alterations in glucose and lipid metabolism and in overall organism energetics. Here, we describe the unique mechanisms by which CMA contributes to the regulation of cellular metabolism and discuss the possible implications of these previously unknown functions of CMA for the pathogenesis of common metabolic diseases.
大多数哺乳动物细胞中存在不同类型的自噬,它们在细胞内降解过程中各自执行非常特定的任务。其中一些自噬途径通过直接水解细胞内的脂质储存和糖原,对细胞代谢产生作用。相比之下,伴侣介导的自噬(CMA)是一种选择性自噬形式,只能将蛋白质靶向溶酶体进行降解。因此,人们曾认为该途径对细胞代谢唯一可能的作用是通过蛋白质分解产生游离氨基酸。然而,最近的研究表明,CMA紊乱会导致葡萄糖和脂质代谢以及整体机体能量代谢发生重要改变。在此,我们描述了CMA参与细胞代谢调节的独特机制,并讨论了CMA这些先前未知功能对常见代谢疾病发病机制的可能影响。