Skaper S D, Moore S E, Walsh F S
Neurology Centre of Excellence for Drug Discovery, GlaxoSmithKline Pharmaceuticals, New Frontiers Science Park, Third Avenue, Essex CM19 5AW, Harlow, UK.
Prog Neurobiol. 2001 Dec;65(6):593-608. doi: 10.1016/s0301-0082(01)00017-x.
During development of the nervous system, neurons extend axons over considerable distances in a highly stereospecific fashion in order to innervate their targets in an appropriate manner. This involves the recognition, by the axonal growth cone, of guidance cues that determine the pathway taken by the axons. These guidance cues can act to promote and/or repel growth cone advance, and they can act either locally or at a distance from their place of synthesis. The directed growth of axons is partly governed by cell adhesion molecules (CAMs) on the neuronal growth cone that bind to CAMs on the surface of other axons or non-neuronal cells. In vitro assays have established the importance of the CAMs (N-CAM, N-cadherin and the L1 glycoprotein) in promoting axonal growth over cells, such as Schwann cells, astrocytes and muscle cells. Strong evidence now exists implicating the fibroblast growth factor receptor tyrosine kinase as the primary signal transduction molecule in the CAM pathway. Cell adhesion molecules are important constituents of synapses, and CAMs appear to play important and diverse roles in regulating synaptic plasticity associated with learning and memory. Negative extracellular signals which physically direct neurite growth have also been described. The latter include the neuronal growth inhibitory proteins Nogo and myelin-associated glycoprotein, as well as the growth cone collapsing Semaphorins/neuropilins. Although less well characterised, evidence is now beginning to emerge describing a role for Rho kinase-mediated signalling in inhibition of neurite outgrowth. This review focuses on some of the major themes and ideas associated with this fast-moving field of neuroscience.
在神经系统发育过程中,神经元以高度立体特异性的方式将轴突延伸相当长的距离,以便以适当的方式支配其靶标。这涉及轴突生长锥识别决定轴突所走路径的导向线索。这些导向线索可促进和/或排斥生长锥前进,它们可在局部起作用,也可在远离其合成部位的地方起作用。轴突的定向生长部分受神经元生长锥上的细胞粘附分子(CAMs)调控,这些分子与其他轴突或非神经元细胞表面的CAMs结合。体外试验已证实CAMs(神经细胞粘附分子、N-钙粘蛋白和L1糖蛋白)在促进轴突在雪旺细胞、星形胶质细胞和肌肉细胞等细胞上生长方面的重要性。现在有强有力的证据表明成纤维细胞生长因子受体酪氨酸激酶是CAM途径中的主要信号转导分子。细胞粘附分子是突触的重要组成部分,并且CAMs似乎在调节与学习和记忆相关的突触可塑性方面发挥重要且多样的作用。也有描述物理上指导神经突生长的负性细胞外信号。后者包括神经元生长抑制蛋白Nogo和髓磷脂相关糖蛋白,以及使生长锥塌陷的信号素/神经纤毛蛋白。虽然其特征描述较少,但现在开始有证据表明Rho激酶介导的信号传导在抑制神经突生长中起作用。本综述重点关注与这个快速发展的神经科学领域相关的一些主要主题和观点。