Cammer W, Sacchi R, Kahn S, Sapirstein V
J Neurosci Res. 1985;14(3):303-16. doi: 10.1002/jnr.490140303.
The spinal cords of young and adult normal and dysmyelinating mutant (shiverer) mice were immunostained with anticarbonic anhydrase to investigate the distribution of oligodendroglial populations into the gray- and white-matter regions in the developing normal and mutant animals; the morphology of oligodendrocytes and their processes at the light microscopic level in gray matter and white matter; and the apparent gliosis in the gray matter, as well as the white matter, of the mutants. Immunocytochemistry and enzyme assays revealed consistent increases in carbonic anhydrase antigenicity and specific activity in controls and mutants between the ages of approximately 15 days and approximately 60 days. As shown previously in adult animals, oligodendroglia in larger than normal proportions were situated at the periphery of the "white-matter" columns, as compared to gray matter, in the shiverers, with, however, significant numbers of oligodendroglia were heterogeneous with respect to shapes, configuration of processes, and intensity of carbonic anhydrase immunostaining. In the shiverer "white matter" the oligodendrocytes were smaller than normal, and their shapes and arrangement were relatively irregular. In the normal gray matter short oligodendroglial processes appeared to be associated with neuronal perikarya, and those processes were more pronounced at approximately 90 days than at approximately 20 days of age. Background staining in normal gray matter suggested that oligodendroglial processes were, in addition, tightly wound around many axons. In shiverer gray matter the oligodendrocytes were smaller, and their processes appeared to be wrapped more loosely around smaller numbers of conspicuous axons and to be associated less frequently with neuronal perikarya. This finding suggests that the deficiency in the myelin basic protein in the mutant may affect interactions between oligodendrocytes and neurons in the gray matter as well as in the white matter. The astrocytic "marker," glial fibrillary acidic protein, was detected in gray and white matter of shiverers as young as 16 days, and the differences from carbonic anhydrase localization supported the conclusion that the processes enwrapping axons in the shiverer mouse CNS are derived from oligodendrocytes, not astrocytes.
用抗碳酸酐酶对幼年和成年正常及髓鞘形成异常突变体(颤抖鼠)小鼠的脊髓进行免疫染色,以研究少突胶质细胞群体在正常发育和突变动物的灰质和白质区域中的分布;在光镜水平下观察灰质和白质中少突胶质细胞及其突起的形态;以及突变体灰质和白质中明显的胶质细胞增生。免疫细胞化学和酶分析显示,在大约15天至大约60天龄之间,对照小鼠和突变体小鼠的碳酸酐酶抗原性和比活性持续增加。如先前在成年动物中所示,与灰质相比,颤抖鼠中比例大于正常的少突胶质细胞位于“白质”柱的周边,然而,大量少突胶质细胞在形状、突起构型和碳酸酐酶免疫染色强度方面存在异质性。在颤抖鼠的“白质”中,少突胶质细胞比正常的小,其形状和排列相对不规则。在正常灰质中,短的少突胶质细胞突起似乎与神经元胞体相关,并且这些突起在大约90天时比在大约20天时更明显。正常灰质中的背景染色表明,少突胶质细胞突起此外还紧密缠绕在许多轴突周围。在颤抖鼠灰质中,少突胶质细胞较小,其突起似乎更松散地包裹在较少数量的明显轴突周围,并且与神经元胞体的关联频率较低。这一发现表明,突变体中髓鞘碱性蛋白的缺乏可能会影响灰质和白质中少突胶质细胞与神经元之间的相互作用。在年仅16天的颤抖鼠的灰质和白质中检测到星形胶质细胞“标记物”胶质纤维酸性蛋白,与碳酸酐酶定位的差异支持了这样的结论,即颤抖鼠中枢神经系统中包裹轴突的突起来源于少突胶质细胞,而非星形胶质细胞。