Department of Neuroscience, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen N, Denmark.
Department of Neuroscience, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen N, Denmark.
Cell Rep. 2021 Apr 13;35(2):108973. doi: 10.1016/j.celrep.2021.108973.
Fast axonal transport of neuropeptide-containing dense core vesicles (DCVs), endolysosomal organelles, and presynaptic components is critical for maintaining neuronal functionality. How the transport of DCVs is orchestrated remains an important unresolved question. The small GTPase Rab2 mediates DCV biogenesis and endosome-lysosome fusion. Here, we use Drosophila to demonstrate that Rab2 also plays a critical role in bidirectional axonal transport of DCVs, endosomes, and lysosomal organelles, most likely by controlling molecular motors. We further show that the lysosomal motility factor Arl8 is required as well for axonal transport of DCVs, but unlike Rab2, it is also critical for DCV exit from cell bodies into axons. We also provide evidence that the upstream regulators of Rab2 and Arl8, Ema and BORC, activate these GTPases during DCV transport. Our results uncover the mechanisms underlying axonal transport of DCVs and reveal surprising parallels between the regulation of DCV and lysosomal motility.
神经肽富含致密核心囊泡(DCVs)、内溶酶体细胞器和突触前成分的快速轴突运输对于维持神经元功能至关重要。DCV 运输如何协调仍然是一个重要的未解决的问题。小分子 GTPase Rab2 介导 DCV 的生物发生和内体-溶酶体融合。在这里,我们使用果蝇证明 Rab2 也在 DCV、内体和溶酶体细胞器的双向轴突运输中发挥关键作用,很可能通过控制分子马达。我们进一步表明,溶酶体运动因子 Arl8 也需要用于 DCV 的轴突运输,但与 Rab2 不同,它对于 DCV 从细胞体进入轴突也很关键。我们还提供了证据表明,Rab2 和 Arl8 的上游调节剂 Ema 和 BORC 在 DCV 运输过程中激活这些 GTPases。我们的研究结果揭示了 DCV 轴突运输的机制,并揭示了 DCV 和溶酶体运动调节之间令人惊讶的相似之处。