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神经元迁移的分子奥秘:粘着斑激酶与细胞周期蛋白依赖性激酶5

The molecular mystery of neuronal migration: FAK and Cdk5.

作者信息

Nikolic Margareta

机构信息

MRC Centre for Developmental Neurobiology, New Hunt's House, King's College London, London SE1 1UL, UK.

出版信息

Trends Cell Biol. 2004 Jan;14(1):1-5. doi: 10.1016/j.tcb.2003.10.010.

DOI:10.1016/j.tcb.2003.10.010
PMID:14729173
Abstract

The basic building blocks of a cell are its cytoskeletal proteins, the orderly but dynamic organization of which is essential. How signalling molecules regulate the cytoskeleton in the developing nervous system is still largely unknown. A recent breakthrough sheds light on a pathway involving Cdk5 (cyclin-dependent kinase 5) and FAK (focal adhesion kinase), demonstrating their role in regulating microtubule structure and thus nuclear positioning in radially migrating cortical neurones.

摘要

细胞的基本组成部分是其细胞骨架蛋白,这些蛋白有序但动态的组织形式至关重要。信号分子如何在发育中的神经系统中调节细胞骨架,目前仍 largely unknown(此处原文有误,应改为“largely unknown”,意为“很大程度上未知”)。最近的一项突破揭示了一条涉及Cdk5(细胞周期蛋白依赖性激酶5)和FAK(粘着斑激酶)的途径,证明了它们在调节微管结构从而在放射状迁移的皮层神经元中调节细胞核定位方面的作用。

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The molecular mystery of neuronal migration: FAK and Cdk5.神经元迁移的分子奥秘:粘着斑激酶与细胞周期蛋白依赖性激酶5
Trends Cell Biol. 2004 Jan;14(1):1-5. doi: 10.1016/j.tcb.2003.10.010.
2
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p39 activates cdk5 in neurons, and is associated with the actin cytoskeleton.p39在神经元中激活细胞周期蛋白依赖性激酶5(cdk5),并与肌动蛋白细胞骨架相关。
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Cyclin-dependent kinase 5/p35 contributes synergistically with Reelin/Dab1 to the positioning of facial branchiomotor and inferior olive neurons in the developing mouse hindbrain.细胞周期蛋白依赖性激酶5/p35与Reelin/Dab1协同作用,参与发育中小鼠后脑面部鳃弓运动神经元和下橄榄核神经元的定位。
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Cdk5 phosphorylation of doublecortin ser297 regulates its effect on neuronal migration.双皮质素丝氨酸297位点的Cdk5磷酸化调节其对神经元迁移的影响。
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