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CRMP4与CRMP2相互作用以协调细胞骨架动力学,调节生长锥发育和轴突伸长。

CRMP4 and CRMP2 Interact to Coordinate Cytoskeleton Dynamics, Regulating Growth Cone Development and Axon Elongation.

作者信息

Tan Minghui, Cha Caihui, Ye Yongheng, Zhang Jifeng, Li Sumei, Wu Fengming, Gong Sitang, Guo Guoqing

机构信息

Department of Anatomy, Medical College of Jinan University, Guangzhou 510630, China ; Postdoctoral Stations of Integrated Traditional and Western Medicine, Medical College of Jinan University, Guangzhou 510630, China.

Department of Pediatrics, The First Affiliated Hospital of Jinan University, Guangzhou 510630, China ; Department of Pediatrics, Guangzhou Women and Children's Medical Center, The Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.

出版信息

Neural Plast. 2015;2015:947423. doi: 10.1155/2015/947423. Epub 2015 May 10.

Abstract

Cytoskeleton dynamics are critical phenomena that underpin many fundamental cellular processes. Collapsin response mediator proteins (CRMPs) are highly expressed in the developing nervous system, mediating growth cone guidance, neuronal polarity, and axonal elongation. However, whether and how CRMPs associate with microtubules and actin coordinated cytoskeletal dynamics remain unknown. In this study, we demonstrated that CRMP2 and CRMP4 interacted with tubulin and actin in vitro and colocalized with the cytoskeleton in the transition-zone in developing growth cones. CRMP2 and CRMP4 also interacted with one another coordinately to promote growth cone development and axonal elongation. Genetic silencing of CRMP2 enhanced, whereas overexpression of CRMP2 suppressed, the inhibitory effects of CRMP4 knockdown on axonal development. In addition, knockdown of CRMP2 or overexpression of truncated CRMP2 reversed the promoting effect of CRMP4. With the overexpression of truncated CRMP2 or CRMP4 lacking the cytoskeleton interaction domain, the promoting effect of CRMP was suppressed. These data suggest a model in which CRMP2 and CRMP4 form complexes to bridge microtubules and actin and thus work cooperatively to regulate growth cone development and axonal elongation.

摘要

细胞骨架动力学是许多基本细胞过程的关键现象。塌陷反应介导蛋白(CRMPs)在发育中的神经系统中高度表达,介导生长锥导向、神经元极性和轴突伸长。然而,CRMPs是否以及如何与微管和肌动蛋白协调细胞骨架动力学相关联仍不清楚。在本研究中,我们证明CRMP2和CRMP4在体外与微管蛋白和肌动蛋白相互作用,并在发育中的生长锥的过渡区与细胞骨架共定位。CRMP2和CRMP4也相互协调作用,以促进生长锥发育和轴突伸长。CRMP2的基因沉默增强了CRMP4敲低对轴突发育的抑制作用,而CRMP2的过表达则抑制了这种作用。此外,CRMP2的敲低或截短型CRMP2的过表达逆转了CRMP4的促进作用。随着截短型CRMP2或缺乏细胞骨架相互作用结构域的CRMP4的过表达,CRMP的促进作用受到抑制。这些数据提示了一个模型,即CRMP2和CRMP4形成复合物以连接微管和肌动蛋白,从而协同调节生长锥发育和轴突伸长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/867e/4442009/4f392e794b41/NP2015-947423.001.jpg

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