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新生大鼠视神经体外微小节段:胶质细胞生成与髓鞘形成

Minisegments of newborn rat optic nerves in vitro: gliogenesis and myelination.

作者信息

Omlin F X, Waldmeyer J

出版信息

Exp Brain Res. 1986;65(1):189-99. doi: 10.1007/BF00243842.

Abstract

The question of whether the development of CNS glial cells requires the presence of axons or not can be studied with in vitro systems. In order to compare the differentiation of glial cells during development in vitro with that in situ, we have selected the optic nerve, which is anatomically as well as histotypically a well defined structure. For the in vitro investigations, small explants, called minisegments, of newborn rat optic nerves were cultivated taking four major conditions into account: the regular size of the minisegments should guarantee a permanent exchange of the culture medium in order to avoid cell death, neither mechanical nor enzymatic dissociation of the tissue were applied, the minisegments were explanted into flasks without substrate for cell adhesion and the minisegments were under constant gyratory agitation. The following in situ results were obtained: optic nerves of newborn rats are morphologically characterized by the presence of naked axons, astrocytes, glial precursors, and the absence of both differentiated oligodendrocytes and myelin. At postnatal day 5 myelin sheaths are still absent. Two weeks after birth, differentiated oligodendrocytes and microglial cells are present and numerous axons are surrounded by compact myelin. The in vitro experiments show the following main results, which were obtained after 14 h, 2 d, 5 d and 14 d in culture: during time in culture, the shape of minisegment of newborn rat optic nerves undergoes drastic changes, which indicate high cellular dynamics. After 14 h in vitro, axonal profiles, cells with pyknotic nuclei as well as clusters of astrocytes and glial precursors are present. After 2 days in culture the axonal profiles disappeared and the number of degenerating cells decreased drastically. Many large cells, probably phagocytes containing inclusions and more cells are differentiated. At the stage of 5 d in vitro 4 major types of cells can be distinguished: differentiated oligodendrocytes, which form compact and loose myelin, astrocytes, large and small glioblasts and phagocytes. Immunoprecipitates for myelin basic protein and/or myelin associated glycoprotein were found in oligodendrocytes, in their processes and associated to the myelin. Processes of some astrocytes showed immunoreactive products of glial fibrillary acidic protein. After two weeks in culture, the minisegments were mostly composed of astrocytes, whereas oligodendrocytes became rare and phagocytes disappeared. It can be concluded that CNS glial cells can attain their structural and immunocytochemical characteristics in the total absence of neuronal cell bodies and axons.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

中枢神经系统胶质细胞的发育是否需要轴突的存在这一问题可以通过体外系统进行研究。为了比较体外发育过程中胶质细胞的分化与原位分化情况,我们选择了视神经,它在解剖学和组织学上都是一个明确的结构。对于体外研究,考虑到四个主要条件来培养新生大鼠视神经的小外植体,即微节段:微节段的常规大小应保证培养基的持续交换以避免细胞死亡,不采用组织的机械或酶解分离,将微节段植入无细胞黏附底物的培养瓶中,且微节段处于持续旋转振荡状态。获得了以下原位结果:新生大鼠的视神经在形态上的特征是存在裸露的轴突、星形胶质细胞、胶质前体细胞,且不存在分化的少突胶质细胞和髓磷脂。出生后第5天仍无髓鞘。出生两周后,出现了分化的少突胶质细胞和小胶质细胞,许多轴突被致密髓磷脂包围。体外实验显示了以下主要结果,这些结果是在培养14小时、2天、5天和14天后获得的:在培养过程中,新生大鼠视神经微节段的形状发生剧烈变化,这表明细胞动力学很高。体外培养14小时后,出现了轴突轮廓、核固缩的细胞以及星形胶质细胞和胶质前体细胞簇。培养2天后,轴突轮廓消失,退化细胞数量急剧减少。许多大细胞,可能是含有内含物的吞噬细胞,并且更多的细胞发生分化。在体外培养5天的阶段,可以区分出4种主要类型的细胞:形成致密和疏松髓磷脂的分化少突胶质细胞、星形胶质细胞、大小胶质母细胞和吞噬细胞。在少突胶质细胞及其突起中以及与髓磷脂相关的部位发现了髓磷脂碱性蛋白和/或髓磷脂相关糖蛋白的免疫沉淀物。一些星形胶质细胞的突起显示出胶质纤维酸性蛋白的免疫反应产物。培养两周后,微节段主要由星形胶质细胞组成,而少突胶质细胞变得稀少,吞噬细胞消失。可以得出结论,在完全没有神经元细胞体和轴突的情况下,中枢神经系统胶质细胞可以获得其结构和免疫细胞化学特征。(摘要截取自400字)

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