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细胞质连接蛋白通过微管和生长锥动力学调节神经元极化。

Cytoplasmic linker proteins regulate neuronal polarization through microtubule and growth cone dynamics.

机构信息

Max Planck Institute of Neurobiology, Junior Research Group Axonal Growth and Regeneration, 82152 Martinsried, Germany.

出版信息

J Neurosci. 2011 Jan 26;31(4):1528-38. doi: 10.1523/JNEUROSCI.3983-10.2011.

Abstract

Axon formation is a hallmark of initial neuronal polarization. This process is thought to be regulated by enhanced microtubule stability in the subsequent axon and changes in actin dynamics in the future axonal growth cone. Here, we show that the microtubule end-binding proteins cytoplasmic linker protein (CLIP)-115 and CLIP-170 were enriched in the axonal growth cone and extended into the actin-rich domain of the growth cone. CLIPs were necessary for axon formation and sufficient to induce an axon. The regulation of axonal microtubule stabilization by CLIPs enabled the protrusion of microtubules into the leading edge of the axonal growth cone. Moreover, CLIPs positively regulated growth cone dynamics and restrained actin arc formation, which was necessary for axon growth. In fact, in neurons without CLIP activity, axon formation was restored by actin destabilization or myosin II inhibition. Together, our data suggest that CLIPs enable neuronal polarization by controlling the stabilization of microtubules and growth cone dynamics.

摘要

轴突形成是初始神经元极化的标志。这一过程被认为是通过后续轴突中微管稳定性的增强和未来轴突生长锥中肌动蛋白动力学的变化来调节的。在这里,我们表明微管末端结合蛋白细胞质连接蛋白 (CLIP)-115 和 CLIP-170 在轴突生长锥中富集,并延伸到生长锥中的富含肌动蛋白的区域。CLIPs 对于轴突的形成是必要的,并且足以诱导轴突。CLIPs 通过调节轴突微管的稳定性,使微管能够突入轴突生长锥的前缘。此外,CLIPs 还正向调节生长锥动力学,并抑制肌动蛋白弧形的形成,这对于轴突的生长是必要的。事实上,在没有 CLIP 活性的神经元中,通过肌动蛋白解稳或肌球蛋白 II 抑制可以恢复轴突的形成。总之,我们的数据表明,CLIPs 通过控制微管的稳定性和生长锥动力学来促进神经元极化。

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