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耦合神经胶质细胞数量与轴突模式。

Coupling glial numbers and axonal patterns.

作者信息

Hidalgo Alicia, Griffiths Rachel

机构信息

NeuroDevelopment Group, School of Biosciences, University of Birmingham, Edgbaston, Birmingham, UK.

出版信息

Cell Cycle. 2004 Sep;3(9):1118-20. Epub 2004 Sep 15.

Abstract

The control of the rate of cell division enables cells to respond to signals from other cells and this promotes the emergence of order as cell mass increases during growth. Glial cell proliferation is coupled to axon guidance, and the sequential deployment of glial cells in constrained numbers enables the sequential sorting out of axons into appropriate trajectories through time.(1) This is achieved by the neuron-dependent regulation of glial division at the G(1) phase. Early on, Prospero plays a key role controlling the G(1) phase and it enables the glia to proliferate in response to neurons. Later, Prospero maintains subsets of glia in G(1) arrest, retaining mitotic potential, whereas non-Prospero glia terminally differentiate. Only this population of Prospero quiescent precursors can overproliferate when neurons are eliminated, inducing a repair response. It is compelling to investigate whether the vertebrate homologue Prox1 may enable the repair response of vertebrate glia.

摘要

细胞分裂速率的控制使细胞能够对来自其他细胞的信号作出反应,并且随着生长过程中细胞质量的增加,这促进了有序状态的出现。神经胶质细胞的增殖与轴突导向相关联,并且以有限数量顺序部署神经胶质细胞能够使轴突随着时间的推移顺序地分选到合适的轨迹中。(1)这是通过神经元在G(1)期对神经胶质细胞分裂的依赖性调节来实现的。早期,Prospero在控制G(1)期方面起着关键作用,并且它使神经胶质细胞能够响应神经元而增殖。后来,Prospero使神经胶质细胞亚群处于G(1)期停滞状态,保留有丝分裂潜能,而非Prospero神经胶质细胞则终末分化。只有当神经元被消除时,这群处于静止状态的Prospero前体细胞才会过度增殖,从而引发修复反应。研究脊椎动物同源物Prox1是否能够使脊椎动物神经胶质细胞产生修复反应是很有意义的。

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