Hatten M E, Mason C A, Liem R K, Edmondson J C, Bovolenta P, Shelanski M L
Cent Nerv Syst Trauma. 1984 Fall;1(1):15-27. doi: 10.1089/cns.1984.1.15.
To study neuron-glial interactions, our laboratory has developed an in vitro model system that, when used with cell type-specific antisera, allows visualization of contacts between cerebellar granule neurons and astroglia. When cells were dissociated from early postnatal mouse cerebellum and plated in microcultures, the neurons aligned along glial filament protein (GFP)-containing astroglial processes. The behavior of the neurons depended on the shape of the particular astroglial cell that they contacted. Neuronal migration commonly occurred along highly elongated astroglial processes of Bergmann-like glia but was inhibited when neurons nestled among the arms of stellate astroglia. To analyze the influence of neurons on the astroglial shapes associated with neuronal migration, cerebellar granule neurons and astroglia were purified and recombined. In the absence of neurons, cerebellar astroglia assumed a flattened shape and proliferated rapidly. In the absence of astroglia, neurite outgrowth was severely impaired. When neurons were recombined with purified astroglia, astroglial proliferation slowed markedly, the shape of the astroglia transformed into complex forms, and neuron-glial interactions were seen. In tissue sections, immature forms of glia were found in the developing cerebellar axon tracts, but no obvious relationship could be discerned between the growing axonal tips and the glia. At P7, a period when the growth of cerebellar axons slows markedly, a transient natural gliosis was seen in the putative white matter. These studies underscore the interdependence of neurons and astroglia during periods of neuron differentiation and neurite outgrowth. In addition, they raise the possibility that the disruption of normal neuronal-astroglial contacts suffered during CNS injury could lead to defects in astroglial form and surface properties that, in turn, might impair axon regrowth.
为了研究神经元与神经胶质细胞的相互作用,我们实验室开发了一种体外模型系统,该系统与细胞类型特异性抗血清一起使用时,可使小脑颗粒神经元与星形胶质细胞之间的接触可视化。当从出生后早期小鼠小脑中分离细胞并接种到微培养物中时,神经元会沿着含有胶质纤维酸性蛋白(GFAP)的星形胶质细胞突起排列。神经元的行为取决于它们所接触的特定星形胶质细胞的形状。神经元迁移通常沿着伯格曼样胶质细胞的高度细长的星形胶质细胞突起发生,但当神经元嵌套在星状星形胶质细胞的臂之间时,迁移会受到抑制。为了分析神经元对与神经元迁移相关的星形胶质细胞形状的影响,对小脑颗粒神经元和星形胶质细胞进行了纯化和重组。在没有神经元的情况下,小脑星形胶质细胞呈扁平状并迅速增殖。在没有星形胶质细胞的情况下,神经突生长严重受损。当神经元与纯化的星形胶质细胞重组时,星形胶质细胞的增殖明显减慢,星形胶质细胞的形状转变为复杂的形式,并且可以看到神经元与神经胶质细胞的相互作用。在组织切片中,在发育中的小脑轴突束中发现了未成熟的胶质细胞形式,但在生长的轴突末端与胶质细胞之间没有明显的关系。在出生后第7天,即小脑轴突生长明显减慢的时期,在假定的白质中出现了短暂的自然胶质增生。这些研究强调了在神经元分化和神经突生长期间神经元与星形胶质细胞的相互依赖性。此外,它们还提出了一种可能性,即中枢神经系统损伤期间正常神经元与星形胶质细胞接触的破坏可能导致星形胶质细胞形态和表面特性的缺陷,进而可能损害轴突再生。