Lewis Tommy L, Mao Tianyi, Svoboda Karel, Arnold Don B
Department of Biological Sciences, University of Southern California, Los Angeles, USA.
Nat Neurosci. 2009 May;12(5):568-76. doi: 10.1038/nn.2318. Epub 2009 Apr 19.
The distinct electrical properties of axonal and dendritic membranes are largely a result of specific transport of vesicle-bound membrane proteins to each compartment. How this specificity arises is unclear because kinesin motors that transport vesicles cannot autonomously distinguish dendritically projecting microtubules from those projecting axonally. We hypothesized that interaction with a second motor might enable vesicles containing dendritic proteins to preferentially associate with dendritically projecting microtubules and avoid those that project to the axon. Here we show that in rat cortical neurons, localization of several distinct transmembrane proteins to dendrites is dependent on specific myosin motors and an intact actin network. Moreover, fusion with a myosin-binding domain from Melanophilin targeted Channelrhodopsin-2 specifically to the somatodendritic compartment of neurons in mice in vivo. Together, our results suggest that dendritic transmembrane proteins direct the vesicles in which they are transported to avoid the axonal compartment through interaction with myosin motors.
轴突膜和树突膜独特的电学特性很大程度上是囊泡结合膜蛋白特异性转运至每个区室的结果。这种特异性是如何产生的尚不清楚,因为运输囊泡的驱动蛋白无法自主区分向树突投射的微管和向轴突投射的微管。我们推测,与第二种驱动蛋白的相互作用可能使含有树突蛋白的囊泡优先与向树突投射的微管结合,并避开那些向轴突投射的微管。在此我们表明,在大鼠皮质神经元中,几种不同跨膜蛋白在树突中的定位依赖于特定的肌球蛋白驱动蛋白和完整的肌动蛋白网络。此外,将来自亲黑素蛋白的肌球蛋白结合结构域与通道视紫红质-2融合,可在体内将其特异性靶向小鼠神经元的胞体-树突区室。我们的结果共同表明,树突跨膜蛋白可引导其所在的运输囊泡通过与肌球蛋白驱动蛋白的相互作用避开轴突区室。