Mason C A, Edmondson J C, Hatten M E
Department of Pathology, Columbia University, College of Physicians and Surgeons, New York, New York 10032.
J Neurosci. 1988 Sep;8(9):3124-34. doi: 10.1523/JNEUROSCI.08-09-03124.1988.
To analyze how astroglial cells attain the complex shapes that support neuronal migration and positioning in vitro (Hatten et al., 1984; Hatten 1985), early postnatal mouse cerebellar cells were plated in microcultures, and glial process outgrowth was monitored by high-resolution time-lapse video microscopy combined with immunocytochemical localization of antisera to glial filament protein (GFP), and by electron microscopy. The 2 principal astroglial forms seen in these cultures, stellate and Bergmann-like (Hatten et al., 1984), begin to develop their distinctive shapes by the outgrowth of processes in the first 8 hr after the cells are plated. Glial process extension is most vigorous in this period, resulting predominantly in stellate forms. A second population of glial cells, having fewer, longer processes reminiscent of Bergmann glia in vivo, first appears about 5 hr after plating. During the next 16-24 hr, while the stellate cells only slightly increase their process length, the bipolar cells double their length. The most striking feature of the elongating glial process is its highly motile tip, which rapidly extends microspikes and lamellopodia. Unlike the neuronal growth cone, which is the expanded terminal of a thin neurite shaft, the glial growing tip forms the end of a wide, paddle-like process that is filled with motile mitochondria and masses of glial filaments, and is bordered by an undulating lamella fringed by microspikes. Soon after the emergence of glial processes, cell-cell interactions between the growing glial process tip and granule neurons occur. Within minutes of an initial encounter between the glial process and the neuron, contact relationships that are stable during the observation period form between the cells. Subsequently, many neurons extend a small neurite onto the glial process, and astroglial process extension continues by the movement of the glial growing tip out beyond the neuron. Thus, cerebellar astroglia in vitro develop complex shapes in the same fashion as do neurons: the outgrowth of processes tipped by a motile ending. The growing tips of astroglial processes interact with neurons, resulting in the stable association of neurons and glia.
为了分析星形胶质细胞如何形成支持神经元在体外迁移和定位的复杂形状(哈滕等人,1984年;哈滕,1985年),将出生后早期的小鼠小脑细胞接种到微培养物中,并通过高分辨率延时视频显微镜结合针对胶质纤维酸性蛋白(GFAP)抗血清的免疫细胞化学定位以及电子显微镜来监测胶质突起的生长。在这些培养物中观察到的两种主要星形胶质细胞形态,即星状和类伯格曼细胞(哈滕等人,1984年),在细胞接种后的最初8小时内通过突起的生长开始形成其独特的形状。在此期间,胶质突起的延伸最为活跃,主要形成星状形态。另一群胶质细胞,其突起较少且较长,类似于体内的伯格曼胶质细胞,在接种后约5小时首次出现。在接下来的16 - 24小时内,星状细胞的突起长度仅略有增加,而双极细胞的突起长度则增加了一倍。伸长的胶质突起最显著的特征是其高度可移动的尖端,该尖端迅速伸出微棘和片状伪足。与神经元生长锥不同,神经元生长锥是细神经突轴的扩张末端,而胶质生长尖端形成一个宽阔的、桨状突起的末端,该突起充满了可移动的线粒体和大量胶质纤维,并由微棘边缘的起伏薄片所界定。胶质突起出现后不久,生长中的胶质突起尖端与颗粒神经元之间就会发生细胞间相互作用。在胶质突起与神经元初次接触后的几分钟内,细胞之间形成了在观察期内稳定的接触关系。随后,许多神经元在胶质突起上伸出一小段神经突,并且胶质突起通过胶质生长尖端向神经元之外的移动而继续延伸。因此,体外培养的小脑星形胶质细胞以与神经元相同的方式形成复杂形状:由可移动末端引导的突起生长。胶质突起的生长尖端与神经元相互作用,导致神经元和胶质细胞的稳定结合。