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轴突形成:神经元极性产生的分子模型。

Axon formation: a molecular model for the generation of neuronal polarity.

作者信息

Andersen S S, Bi G Q

机构信息

University of California San Diego, Department of Biology, La Jolla, CA 92093-0357, USA.

出版信息

Bioessays. 2000 Feb;22(2):172-9. doi: 10.1002/(SICI)1521-1878(200002)22:2<172::AID-BIES8>3.0.CO;2-Q.

Abstract

Neurons have unique structural and functional polarity. In general, information flows from the short dendrites to the long axon, and each neuron has multiple dendrites but only one axon. A detailed description of the cellular events leading to the establishment of axonal-dendritic polarity has been given from an in vitro hippocampal culture model system. Little is known, however, about the nature of the underlying molecular events. New data strongly suggest that actin depolymerization at a growth cone is crucial for axon fate determination. We hypothesize that an autocatalytic positive feedback loop at all growth cones locally regulates actin dynamics and other cellular events required for axon formation. Meanwhile, a negative feedback signal, produced by the positive feedback loop, propagates from all growth cones throughout the neuron and counteracts the positive feedback loops. Such feedback regulation provides a robust mechanism for spontaneous symmetry breaking and the formation of only one axon, even in a symmetric in vitro environment. Based on data from studies of cell migration, axon guidance, vesicle exocytosis, and the regulation of actin and microtubule polymerization, we propose a molecular scheme for the positive feedback loop and discuss possible negative feedback signals. BioEssays 22:172-179, 2000.

摘要

神经元具有独特的结构和功能极性。一般来说,信息从短的树突流向长的轴突,并且每个神经元有多个树突但只有一个轴突。从体外海马培养模型系统已经对导致轴突 - 树突极性建立的细胞事件进行了详细描述。然而,对于潜在分子事件的本质却知之甚少。新数据强烈表明生长锥处的肌动蛋白解聚对于轴突命运的决定至关重要。我们假设所有生长锥处的自催化正反馈环局部调节肌动蛋白动力学以及轴突形成所需的其他细胞事件。同时,由正反馈环产生的负反馈信号从所有生长锥传播到整个神经元并抵消正反馈环。这种反馈调节为自发对称性破缺以及即使在对称的体外环境中也仅形成一个轴突提供了一种强大的机制。基于细胞迁移、轴突导向、囊泡胞吐作用以及肌动蛋白和微管聚合调节的研究数据,我们提出了正反馈环的分子机制并讨论了可能的负反馈信号。《生物论文》22:172 - 179,2000年。

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