Shim Su Yeon, Wang Jian, Asada Naoyuki, Neumayer Gernot, Tran Hong Chi, Ishiguro Kei-ichiro, Sanada Kamon, Nakatani Yoshihiro, Nguyen Minh Dang
Hotchkiss Brain Institute, Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada T2N 4N1.
J Neurosci. 2008 Apr 2;28(14):3604-14. doi: 10.1523/JNEUROSCI.5278-07.2008.
There is an increasing body of literature pointing to cytoskeletal proteins as spatial organizers and interactors of organelles. In this study, we identified protein 600 (p600) as a novel microtubule-associated protein (MAP) developmentally regulated in neurons. p600 exhibits the unique feature to interact with the endoplasmic reticulum (ER). Silencing of p600 by RNA interference (RNAi) destabilizes neuronal processes in young primary neurons undergoing neurite extension and containing scarce staining of the ER marker Bip. Furthermore, in utero electroporation of p600 RNAi alters neuronal migration, a process that depends on synergistic actions of microtubule dynamics and ER functions. p600-depleted migrating neurons display thin, crooked, and "zigzag" leading process with very few ER membranes. Thus, p600 constitutes the only known MAP to associate with the ER in neurons, and this interaction may impact on multiple cellular processes ranging from neuronal development to neuronal maturation and plasticity.
越来越多的文献表明细胞骨架蛋白是细胞器的空间组织者和相互作用者。在本研究中,我们鉴定出蛋白600(p600)是一种在神经元中受发育调控的新型微管相关蛋白(MAP)。p600具有与内质网(ER)相互作用的独特特征。通过RNA干扰(RNAi)使p600沉默会破坏正在进行神经突延伸且内质网标记物Bip染色稀少的年轻原代神经元中的神经突。此外,在子宫内电穿孔p600 RNAi会改变神经元迁移,这一过程依赖于微管动力学和内质网功能的协同作用。p600缺失的迁移神经元显示出非常薄、弯曲且呈“之字形”的引导突,内质网膜极少。因此,p600是已知的唯一一种在神经元中与内质网相关的MAP,这种相互作用可能会影响从神经元发育到神经元成熟和可塑性的多个细胞过程。