Telethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy.
Department of Medical and Translational Science, University of Naples "Federico II", Naples, Italy.
EMBO J. 2020 Mar 2;39(5):e104546. doi: 10.15252/embj.2020104546. Epub 2020 Feb 19.
To maintain cellular homeostasis, the endoplasmic reticulum (ER) necessitates a continuous removal of ER fragments via a selective, receptor-mediated, form of autophagy known as ER-phagy. In this issue of The EMBO Journal, Jiang et al (2020) shed light on how the best characterized autophagy receptor FAM134B mediates ER membrane fragmentation, the earliest event during ER-phagy. They propose a dynamic model for FAM134B protein oligomerization and ER membrane scission, which are driven by CAMK2B-mediated phosphorylation of the receptor and are altered in sensory neuropathy.
为了维持细胞内环境稳定,内质网(ER)需要通过一种选择性的、受体介导的自噬形式来不断清除 ER 片段,这种自噬形式被称为 ER 自噬。在本期《欧洲分子生物学组织杂志》中,Jiang 等人揭示了如何通过 FAM134B 介导 ER 膜碎片化,这是 ER 自噬的最早事件。他们提出了一个 FAM134B 蛋白寡聚化和 ER 膜分裂的动态模型,该模型由 CAMK2B 介导的受体磷酸化驱动,并在感觉神经病中发生改变。