Department of Cell Biology, Dorris Neuroscience Center, The Scripps Research Institute, La Jolla, California 92037, USA.
Dev Neurobiol. 2011 Nov;71(11):889-900. doi: 10.1002/dneu.20946.
Extracellular matrix (ECM) glycoproteins are expressed in the central nervous system (CNS) in complex and developmentally regulated patterns. The ECM provides a number of critical functions in the CNS, contributing both to the overall structural organization of the CNS and to control of individual cells. At the cellular level, the ECM affects its functions by a wide range of mechanisms, including providing structural support to cells, regulating the activity of second messenger systems, and controlling the distribution and local concentration of growth and differentiation factors. Perhaps the most well known role of the ECM is as a substrate on which motile cells can migrate. Genetic, cell biological, and biochemical studies provide strong evidence that ECM glycoproteins such as laminins, tenascins, and proteoglycans control neuronal migration and positioning in several regions of the developing and adult brain. Recent findings have also shed important new insights into the cellular and molecular mechanisms by which reelin regulates migration. Here we will summarize these findings, emphasizing the emerging concept that ECM glycoproteins promote different modes of neuronal migration such as radial, tangential, and chain migration. We also discuss several studies demonstrating that mutations in ECM glycoproteins can alter neuronal positioning by cell nonautonomous mechanisms that secondarily affect migrating neurons.
细胞外基质 (ECM) 糖蛋白在中枢神经系统 (CNS) 中以复杂且发育调控的模式表达。ECM 在 CNS 中提供了许多关键功能,不仅对 CNS 的整体结构组织有贡献,还对单个细胞的功能有控制作用。在细胞水平上,ECM 通过多种机制影响其功能,包括为细胞提供结构支持、调节第二信使系统的活性,以及控制生长和分化因子的分布和局部浓度。也许 ECM 最广为人知的作用是作为运动细胞可以迁移的基质。遗传、细胞生物学和生物化学研究为 ECM 糖蛋白(如层粘连蛋白、腱糖蛋白和蛋白聚糖)控制发育中和成年大脑的几个区域的神经元迁移和定位提供了强有力的证据。最近的发现也为 reelin 调节迁移的细胞和分子机制提供了重要的新见解。在这里,我们将总结这些发现,强调新兴的概念,即 ECM 糖蛋白促进不同模式的神经元迁移,如放射状、切线状和链状迁移。我们还讨论了几项研究,这些研究表明 ECM 糖蛋白的突变可以通过非细胞自主机制改变神经元的定位,这些机制会间接地影响迁移中的神经元。