Bolz J, Castellani V, Mann F, Henke-Fahle S
INSERM Unité 371 Cerveau et Vision, Lyon/Bron, France.
Prog Brain Res. 1996;108:41-54. doi: 10.1016/s0079-6123(08)62531-5.
One of the basic tasks of neurobiology is to understand how the precision and specificity of neuronal connections is achieved during development. In this paper we reviewed some recent in vitro studies on the developing mammalian cerebral cortex that have been made towards this end. The results of these experiments provided evidence that membrane-associated molecules are instrumental for the formation of specific afferent and efferent cortical projections. Substrate-bound molecules guide growing axons towards their target, regulate the timing of thalamocortical innervation and mediate target cell recognition. Moreover, a newly described glycoprotein, defined by a monoclonal antibody, revealed a molecular heterogeneity in the developing white matter. Since this molecule has opposite effects on thalamic and cortical axons, it might play a role in the segregation of axons running to and from the cortex. Substrate-bound cues are important during the formation of local cortical circuits. In vitro assays demonstrated that molecular components confined to individual cortical layers control the laminar specificity of cortical axon branching. This suggests that similar developmental strategies contribute to the laminar specification of extrinsic and intrinsic cortical circuits. Thus substrate-bound molecules might provide the framework for subsequent activity-dependent mechanisms that control the elaboration of precise connections between the cortical columns. A major challenge ahead is to identify the factors that mediate these processes and to determine their mode of action. Recently, two families of proteins, the netrins and the semaphorins/collapsins, have been identified as growth cone signals in the developing spinal cord (reviewed in Goodman, 1994; Colamarino and Tessier-Lavigne, 1995a; Dodd and Schuchardt, 1995; Kennedy and Tessier-Lavigne, 1995). Semaphorins/collapsins appear to regulate axonal guidance by repelling growth cones and by inhibiting axonal branching and synapse formation. Originally, netrins have been purified as diffusible chemoattractants for commissural axons of the dorsal spinal cord, but it is now well established that they can also function as chemorepellent factors for other classes of neurons. Since netrins are related to extracellular matrix components and since they can bind to the cell surface, they might also act as local guidance cues. A possible role of netrins and semaphorins/collapsins in the development of cortical connections is likely to be resolved in the near future. The identification of the factors that regulate specific branching patterns of cortical neurons might provide a better understanding of cortical development, but it might also be relevant to some aspects of plasticity and repair in the adult cortex.
神经生物学的基本任务之一是了解在发育过程中神经元连接的精确性和特异性是如何实现的。在本文中,我们回顾了一些近期针对此目的而进行的关于发育中的哺乳动物大脑皮层的体外研究。这些实验结果表明,膜相关分子对特定传入和传出皮层投射的形成具有重要作用。底物结合分子引导生长中的轴突朝向其靶标,调节丘脑皮质神经支配的时间,并介导靶细胞识别。此外,一种由单克隆抗体定义的新描述的糖蛋白揭示了发育中的白质中的分子异质性。由于该分子对丘脑和皮层轴突具有相反的作用,它可能在往返皮层的轴突分离中发挥作用。底物结合线索在局部皮层回路的形成过程中很重要。体外实验表明,局限于各个皮层层的分子成分控制着皮层轴突分支的层特异性。这表明类似的发育策略有助于外在和内在皮层回路的层特异性。因此,底物结合分子可能为随后控制皮层柱之间精确连接形成的活动依赖机制提供框架。未来的一个主要挑战是确定介导这些过程的因素并确定它们的作用方式。最近,两类蛋白质,即网蛋白和信号素/塌陷素,已被确定为发育中的脊髓中的生长锥信号(见古德曼,1994年;科拉马里诺和泰西耶 - 拉维涅,1995a;多德和舒查特,1995;肯尼迪和泰西耶 - 拉维涅,1995年的综述)。信号素/塌陷素似乎通过排斥生长锥以及抑制轴突分支和突触形成来调节轴突导向。最初,网蛋白被纯化作为脊髓背侧连合轴突的可扩散化学吸引剂,但现在已经明确它们也可以作为其他类型神经元的化学排斥因子发挥作用。由于网蛋白与细胞外基质成分相关,并且它们可以结合到细胞表面,它们也可能作为局部导向线索。网蛋白和信号素/塌陷素在皮层连接发育中的可能作用在不久的将来可能会得到解决。确定调节皮层神经元特定分支模式的因素可能有助于更好地理解皮层发育,但它也可能与成年皮层可塑性和修复的某些方面相关。