Debbage P L
J Neurol Sci. 1986 Feb;72(2-3):319-36. doi: 10.1016/0022-510x(86)90019-5.
During postnatal development of the higher vertebrate CNS, large populations of oligodendroglia are generated from precursor cells in a very dependable way. In adult lesioned CNS tissues, local populations of oligodendroglia are replenished by proliferation of this replenishment varies from one species to another and also from one lesion type another. Studies on the developmental generation of oligodendroglia are reviewed here, delineating what is known of the early relationships between the CNS glial lineages and of what regulates this development. Contributions from recent cell biological work are considered against the background of morphological and radioautographic results. The quiescent condition of extremely slow turnover in the normal adult CNS is noted, and the dramatic effects of lesions on the neural cell environment are considered. Lesions can trigger proliferation at a much greater rate in the mature oligodendroglial population, as observed both in situ and in tissue culture; in addition to persisting stem cells, the mature cells participate in replenishing the local oligodendroglial population. This regeneration from cells already committed to the oligodendroglial lineage may minimise such disturbing effects of the lesion environment as might distort replenishment of the population from precursor cells.
在高等脊椎动物中枢神经系统(CNS)的出生后发育过程中,大量少突胶质细胞以前体细胞非常可靠的方式产生。在成年受损的CNS组织中,少突胶质细胞的局部群体通过这种增殖得到补充,这种补充在不同物种之间以及不同损伤类型之间各不相同。本文综述了关于少突胶质细胞发育生成的研究,阐述了已知的CNS胶质细胞谱系之间的早期关系以及调节这种发育的因素。近期细胞生物学研究成果是在形态学和放射自显影结果的背景下进行考量的。文中指出了正常成年CNS中极低周转率的静止状态,并考虑了损伤对神经细胞环境的显著影响。如在原位和组织培养中所观察到的,损伤可在成熟少突胶质细胞群体中引发更高的增殖速率;除了持续存在的干细胞外,成熟细胞也参与补充局部少突胶质细胞群体。这种来自已确定为少突胶质细胞谱系的细胞的再生,可能会将损伤环境中可能扭曲前体细胞对群体补充的干扰效应降至最低。