Chino Haruka, Mizushima Noboru
Department of Biochemistry and Molecular Biology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Department of Biochemistry and Molecular Biology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Trends Cell Biol. 2020 May;30(5):384-398. doi: 10.1016/j.tcb.2020.02.001. Epub 2020 Mar 2.
The endoplasmic reticulum (ER) is the largest organelle in cells and has fundamental functions, such as folding, processing, and trafficking of proteins, cellular metabolism, and ion storage. To maintain its function, it is turned over constitutively, and even more actively under certain stress conditions. Quality control of the ER is mediated primarily by two pathways: the ubiquitin-proteasome system and autophagy (termed 'ER-phagy'). The identification of ER-phagy adaptor molecules has shed light on the mechanisms and physiological significance of ER-phagy. Here, we describe recent findings on various types of ER-phagy and present unanswered questions related to their mechanism and regulation.
内质网(ER)是细胞中最大的细胞器,具有折叠、加工和运输蛋白质、细胞代谢以及离子储存等基本功能。为维持其功能,内质网会持续更新,在某些应激条件下更新更为活跃。内质网的质量控制主要由两条途径介导:泛素-蛋白酶体系统和自噬(称为“内质网自噬”)。内质网自噬衔接分子的鉴定揭示了内质网自噬的机制和生理意义。在此,我们描述了关于各种类型内质网自噬的最新发现,并提出了与其机制和调控相关的未解决问题。