a Department of Biochemistry and Molecular Biology , Graduate School and Faculty of Medicine, The University of Tokyo , Tokyo , Japan.
b Department of Computational Biology and Medical Sciences , Graduate School of Frontier Sciences, The University of Tokyo , Tokyo , Japan.
Autophagy. 2017 Jul 3;13(7):1252-1253. doi: 10.1080/15548627.2017.1319041. Epub 2017 May 24.
Although the autophagy-related (ATG) conjugation systems are thought to be important for a late step of autophagosome formation, their precise function has been poorly understood because they are also required for localization of the most important autophagosomal marker LC3. In our recent study we found that, using the autophagosomal SNARE STX17 (syntaxin 17) as an alternative marker, autophagosome-like structures were generated in ATG conjugation system-deficient cells. Those structures could fuse with lysosomes but the degradation of the inner autophagosomal membrane was significantly delayed. We suggest that the ATG conjugation-dependent closure of autophagosomes causes the inner autophagosomal membrane to become sensitive to lysosomal degradation.
虽然自噬相关(ATG)连接系统被认为对自噬体形成的后期步骤很重要,但由于它们也是最重要的自噬体标记 LC3 定位所必需的,因此其确切功能仍知之甚少。在我们最近的研究中,我们发现,使用自噬体 SNARE STX17(突触融合蛋白 17)作为替代标记,在 ATG 连接系统缺陷细胞中会产生类似于自噬体的结构。这些结构可以与溶酶体融合,但内自噬体膜的降解明显延迟。我们认为,ATG 连接依赖性的自噬体闭合导致内自噬体膜对溶酶体降解变得敏感。