Department of Biology, Drexel University, Philadelphia, PA 19104, USA.
Cell Biology, Department of Biology, Utrecht University, Utrecht 3584 CH, the Netherlands.
Dev Cell. 2018 Jul 16;46(2):204-218.e7. doi: 10.1016/j.devcel.2018.06.013.
Neuronal function requires axon-dendrite membrane polarity, which depends on sorting of membrane traffic during entry into axons. Due to a microtubule network of mixed polarity, dendrites receive vesicles from the cell body without apparent capacity for directional sorting. We found that, during entry into dendrites, axonally destined cargos move with a retrograde bias toward the cell body, while dendritically destined cargos are biased in the anterograde direction. A microtubule-associated septin (SEPT9), which localizes specifically in dendrites, impedes axonal cargo of kinesin-1/KIF5 and boosts kinesin-3/KIF1 motor cargo further into dendrites. In neurons and in vitro single-molecule motility assays, SEPT9 suppresses kinesin-1/KIF5 and enhances kinesin-3/KIF1 in a manner that depends on a lysine-rich loop of the kinesin motor domain. This differential regulation impacts partitioning of neuronal membrane proteins into axons-dendrites. Thus, polarized membrane traffic requires sorting during entry into dendrites by a septin-mediated mechanism that bestows directional bias on microtubules of mixed orientation.
神经元功能需要轴突-树突膜极性,这取决于进入轴突过程中膜运输的分拣。由于微管网络具有混合极性,树突从细胞体接收囊泡,而没有明显的定向分拣能力。我们发现,在进入树突的过程中,定向到轴突的货物向细胞体呈逆行偏倚移动,而定向到树突的货物则呈顺行偏倚。一种特异性定位于树突的微管相关 septin(SEPT9),阻碍了驱动蛋白-1/KIF5 的轴突货物,并进一步将驱动蛋白-3/KIF1 向树突推进。在神经元和体外单分子运动分析中,SEPT9 以依赖于驱动蛋白运动结构域中富含赖氨酸的环的方式抑制驱动蛋白-1/KIF5 并增强驱动蛋白-3/KIF1。这种差异调节影响神经元膜蛋白在轴突-树突之间的分区。因此,极化的膜运输需要通过一种由 septin 介导的机制在进入树突时进行分拣,该机制赋予混合取向的微管以方向偏倚。