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肌球蛋白-V 诱导货物在轴突起始段固定和聚集。

Myosin-V Induces Cargo Immobilization and Clustering at the Axon Initial Segment.

作者信息

Janssen Anne F J, Tas Roderick P, van Bergeijk Petra, Oost Rosalie, Hoogenraad Casper C, Kapitein Lukas C

机构信息

Cell Biology, Department of Biology, Faculty of Science, Utrecht UniversityUtrecht, Netherlands.

出版信息

Front Cell Neurosci. 2017 Aug 28;11:260. doi: 10.3389/fncel.2017.00260. eCollection 2017.

Abstract

The selective transport of different cargoes into axons and dendrites underlies the polarized organization of the neuron. Although it has become clear that the combined activity of different motors determines the destination and selectivity of transport, little is known about the mechanistic details of motor cooperation. For example, the exact role of myosin-V in opposing microtubule-based axon entries has remained unclear. Here we use two orthogonal chemically-induced heterodimerization systems to independently recruit different motors to cargoes. We find that recruiting myosin-V to kinesin-propelled cargoes at approximately equal numbers is sufficient to stall motility. Kinesin-driven cargoes entering the axon were arrested in the axon initial segment (AIS) upon myosin-V recruitment and accumulated in distinct actin-rich hotspots. Importantly, unlike proposed previously, myosin-V did not return these cargoes to the cell body, suggesting that additional mechanism are required to establish cargo retrieval from the AIS.

摘要

不同货物选择性运输到轴突和树突中是神经元极化组织的基础。尽管已经明确不同分子马达的联合活动决定了运输的目的地和选择性,但对于分子马达协作的机制细节却知之甚少。例如,肌球蛋白-V在对抗基于微管的轴突进入过程中的确切作用仍不清楚。在这里,我们使用两个正交的化学诱导异源二聚化系统,将不同的分子马达独立招募到货物上。我们发现,以大致相等的数量将肌球蛋白-V招募到由驱动蛋白推动的货物上足以使运动停滞。当招募肌球蛋白-V时,进入轴突的由驱动蛋白驱动的货物在轴突起始段(AIS)被阻滞,并聚集在不同的富含肌动蛋白的热点区域。重要的是,与之前提出的不同,肌球蛋白-V并没有将这些货物运回细胞体,这表明需要额外的机制来建立从AIS的货物回收。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8eb3/5581344/2dced45dca0c/fncel-11-00260-g0001.jpg

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