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微管负端结合蛋白 CAMSAP2 控制着轴突的特化和树突的发育。

Microtubule minus-end binding protein CAMSAP2 controls axon specification and dendrite development.

机构信息

Cell Biology, Faculty of Science, Utrecht University, 3584 CH, Utrecht, The Netherlands; Department of Neuroscience, Erasmus Medical Center, 3015 GE Rotterdam, The Netherlands.

Cell Biology, Faculty of Science, Utrecht University, 3584 CH, Utrecht, The Netherlands.

出版信息

Neuron. 2014 Jun 4;82(5):1058-73. doi: 10.1016/j.neuron.2014.04.019.

Abstract

In neurons, most microtubules are not associated with a central microtubule-organizing center (MTOC), and therefore, both the minus and plus-ends of these non-centrosomal microtubules are found throughout the cell. Microtubule plus-ends are well established as dynamic regulatory sites in numerous processes, but the role of microtubule minus-ends has remained poorly understood. Using live-cell imaging, high-resolution microscopy, and laser-based microsurgery techniques, we show that the CAMSAP/Nezha/Patronin family protein CAMSAP2 specifically localizes to non-centrosomal microtubule minus-ends and is required for proper microtubule organization in neurons. CAMSAP2 stabilizes non-centrosomal microtubules and is required for neuronal polarity, axon specification, and dendritic branch formation in vitro and in vivo. Furthermore, we found that non-centrosomal microtubules in dendrites are largely generated by γ-Tubulin-dependent nucleation. We propose a two-step model in which γ-Tubulin initiates the formation of non-centrosomal microtubules and CAMSAP2 stabilizes the free microtubule minus-ends in order to control neuronal polarity and development.

摘要

在神经元中,大多数微管都不与中央微管组织中心(MTOC)相关联,因此,这些非中心体微管的正负端都存在于整个细胞中。微管的正端在许多过程中被很好地确立为动态调节位点,但微管负端的作用仍然知之甚少。通过活细胞成像、高分辨率显微镜和基于激光的显微手术技术,我们表明 CAMSAP/Nezha/Patronin 家族蛋白 CAMSAP2 特异性定位于非中心体微管的负端,并且是神经元中微管组织所必需的。CAMSAP2 稳定非中心体微管,并且是神经元极性、轴突特化和体外及体内树突分支形成所必需的。此外,我们发现树突中的非中心体微管主要是由 γ-微管蛋白依赖性核形成产生的。我们提出了一个两步模型,其中 γ-微管蛋白启动非中心体微管的形成,而 CAMSAP2 稳定游离微管的负端,以控制神经元极性和发育。

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