a Department of Neuroscience, The Faculty of Health Sciences , University of Copenhagen , Copenhagen , Denmark.
Autophagy. 2018;14(9):1520-1542. doi: 10.1080/15548627.2018.1458170. Epub 2018 Aug 13.
Rab2 is a conserved Rab GTPase with a well-established role in secretory pathway function and phagocytosis. Here we demonstrate that Drosophila Rab2 is recruited to late endosomal membranes, where it controls the fusion of LAMP-containing biosynthetic carriers and lysosomes to late endosomes. In contrast, the lysosomal GTPase Gie/Arl8 is only required for late endosome-lysosome fusion, but not for the delivery of LAMP to the endocytic pathway. We also find that Rab2 is required for the fusion of autophagosomes to the endolysosomal pathway, but not for the biogenesis of lysosome-related organelles. Surprisingly, Rab2 does not rely on HOPS-mediated vesicular fusion for recruitment to late endosomal membranes. Our work suggests that Drosophila Rab2 is a central regulator of the endolysosomal and macroautophagic/autophagic pathways by controlling the major heterotypic fusion processes at the late endosome.
Rab2 是一种保守的 Rab GTPase,在分泌途径功能和吞噬作用中具有明确的作用。在这里,我们证明果蝇 Rab2 被招募到晚期内体膜上,在那里它控制含有 LAMP 的生物合成载体与溶酶体与晚期内体的融合。相比之下,溶酶体 GTPase Gie/Arl8 仅需要用于晚期内体-溶酶体融合,但不需要将 LAMP 递送至内吞途径。我们还发现 Rab2 对于自噬体与内溶酶体途径的融合是必需的,但对于溶酶体相关细胞器的生物发生不是必需的。令人惊讶的是,Rab2 不依赖于 HOPS 介导的囊泡融合来招募晚期内体膜。我们的工作表明,果蝇 Rab2 通过控制晚期内体的主要异型融合过程,是内溶酶体和巨自噬/自噬途径的中央调节剂。