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在海马神经元发育过程中,RhoA、Rac1和cdc42的细胞内分布发生改变。

RhoA, Rac1, and cdc42 intracellular distribution shift during hippocampal neuron development.

作者信息

Santos Da Silva Jorge, Schubert Vanessa, Dotti Carlos G

机构信息

Cavalieri Ottolenghi Scientific Institute, Universita Degli Studi di Torino Torino, Italy.

出版信息

Mol Cell Neurosci. 2004 Sep;27(1):1-7. doi: 10.1016/j.mcn.2004.03.008.

Abstract

Differences in cytoskeleton organization are key determinants of the architecture and dynamics of axons and dendrites. This is most clearly illustrated by the diverse pools of microtubule-associated proteins in axons and dendrites. Whether similar polarized organization occurs for actin regulatory proteins remains to be determined. To address this issue, we analyzed the intracellular distribution of the Rho GTPases, RhoA, Rac1, and cdc42 in hippocampal neurons in culture. We report that all three Rho members are evenly distributed during the time of axon and dendrite sprouting. This is not the case in mature neurons, as RhoA enriches in dendrites, Rac1 in axons, and Cdc42 is equally abundant in both domains. Polarized segregation of the actin regulatory machinery in mature neurons might play an important role in axonal and dendritic architectural plasticity.

摘要

细胞骨架组织的差异是轴突和树突的结构及动态变化的关键决定因素。轴突和树突中微管相关蛋白的不同库最清楚地说明了这一点。肌动蛋白调节蛋白是否也存在类似的极化组织尚待确定。为了解决这个问题,我们分析了培养的海马神经元中Rho GTPases、RhoA、Rac1和cdc42的细胞内分布。我们报告称,在轴突和树突萌发期间,所有这三种Rho成员均呈均匀分布。在成熟神经元中情况并非如此,因为RhoA在树突中富集,Rac1在轴突中富集,而Cdc42在这两个区域中的含量相当。成熟神经元中肌动蛋白调节机制的极化分离可能在轴突和树突的结构可塑性中发挥重要作用。

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