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表达神经元微管相关蛋白的细胞中的细胞骨架可塑性。

Cytoskeletal plasticity in cells expressing neuronal microtubule-associated proteins.

作者信息

Kaech S, Ludin B, Matus A

机构信息

Friedrich Miescher Institute, Basel, Switzerland.

出版信息

Neuron. 1996 Dec;17(6):1189-99. doi: 10.1016/s0896-6273(00)80249-4.

Abstract

MAP2 and tau are the two most prominent neuron-specific microtubule-associated proteins. They have been implicated in the stabilization of microtubules and consequently of neurite morphology. To investigate their influence on microtubule dynamics, we have tagged both proteins with green fluorescent protein and expressed them in non-neuronal cells. Time-lapse recordings of living cells showed that MAP2 and tau did not significantly affect the rates of microtubule growth and shrinkage. Longer recordings revealed the growth and disappearance of MAP-induced microtubule bundles coinciding with changes in cell shape. This supports the idea that microtubule dynamics are influenced by the cortical cytoskeleton. The dynamics-preserving stabilization of microtubules by MAP2 and tau thus provides a molecular basis for the morphological plasticity reported to exist in established neurites.

摘要

微管相关蛋白2(MAP2)和微管蛋白(tau)是两种最显著的神经元特异性微管相关蛋白。它们与微管的稳定以及神经突形态的稳定有关。为了研究它们对微管动力学的影响,我们用绿色荧光蛋白标记了这两种蛋白,并在非神经元细胞中进行表达。活细胞的延时记录显示,MAP2和tau对微管的生长和收缩速率没有显著影响。更长时间的记录揭示了MAP诱导的微管束的生长和消失与细胞形状的变化相一致。这支持了微管动力学受皮质细胞骨架影响的观点。因此,MAP2和tau对微管的动力学保持稳定为已建立的神经突中存在的形态可塑性提供了分子基础。

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