Knapp P E, Skoff R P, Redstone D W
J Neurosci. 1986 Oct;6(10):2813-22. doi: 10.1523/JNEUROSCI.06-10-02813.1986.
Neuroglial cell death was investigated in 3 white matter tracts of jimpy and normal mice. In normal animals, glial death during development ranged from 0.5 to 2.7% of the total glial population. The number of dying glial cells was significantly higher in jimpy animals at times corresponding with oligodendroglial proliferation and the onset of myelination in each tract. At certain ages, over 10% of the glial population were pyknotic at the light-microscopic level. Dying glial cells that were identified ultrastructurally presented the characteristics of oligodendrocytes. Premature death of oligodendrocytes presents a simple explanation for the gross deficits of myelin in jimpy animals. The shortened life span of the jimpy oligodendrocyte may preclude the elaboration of a normal myelin sheath. The jimpy model may prove to be a valuable tool in delineating a role for normal neuroglial cell death during the development of the nervous system.
在jimpy小鼠和正常小鼠的3个白质束中研究了神经胶质细胞死亡情况。在正常动物中,发育过程中的胶质细胞死亡占胶质细胞总数的0.5%至2.7%。在每个白质束中,与少突胶质细胞增殖和髓鞘形成开始相对应的时期,jimpy小鼠中死亡的胶质细胞数量显著更高。在特定年龄,光镜下超过10%的胶质细胞呈固缩状态。超微结构鉴定出的死亡胶质细胞呈现少突胶质细胞的特征。少突胶质细胞的过早死亡为jimpy小鼠髓鞘的严重缺陷提供了一个简单的解释。jimpy少突胶质细胞缩短的寿命可能妨碍正常髓鞘的形成。jimpy模型可能被证明是在描绘正常神经胶质细胞死亡在神经系统发育过程中的作用方面的一个有价值的工具。