Franklin R J, Blakemore W F
MRC Cambridge Centre for Brain Repair, University of Cambridge, UK.
J Anat. 1997 Jan;190 ( Pt 1)(Pt 1):23-33. doi: 10.1046/j.1469-7580.1997.19010023.x.
This review covers a number of aspects of the behaviour of oligodendrocyte progenitors following transplantation into the adult CNS. First, an account is given of the ability of transplanted oligodendrocyte progenitors, grown in tissue culture in the presence of PDGF and bFGF, to extensively remyelinate focal areas of persistent demyelination. Secondly, we describe how transplanted clonal cell lines of oligodendrocyte progenitors will differentiate into astrocytes as well oligodendrocytes following transplantation into pathological environments in which both oligodendrocytes and astrocytes are absent, thereby manifesting the bipotentially demonstrable in vitro but not during development. Finally, a series of studies examining the migratory behaviour of transplanted oligodendrocyte progenitors (modelled using the oliodendrocyte progenitor cell line CG4) are described. These show that CG4 cells do not survive (or migrate) when transplanted into the normal adult CNS. However, if they are transplanted into CNS tissue that has previously been exposed to 40 Gy of x-irradiation then transplanted CG4 cells survive, divide and migrate over large distances. Moreover, within an x-irradiated environment, migrating transplanted CG4 cells are able to enter remotely located foci of demyelination and contribute to the remyelination of the demyelinated axons within. These studies demonstrate that although the normal adult CNS does not appear to support survival and migration of the CG4 cell line, it is possible to manipulate the environment in such a way that these nonpermissive properties of the environment can be overcome.
本综述涵盖了少突胶质前体细胞移植到成年中枢神经系统后的多个行为方面。首先,介绍了在血小板衍生生长因子(PDGF)和碱性成纤维细胞生长因子(bFGF)存在的情况下,在组织培养中生长的移植少突胶质前体细胞对持续性脱髓鞘的局灶区域进行广泛髓鞘再生的能力。其次,我们描述了少突胶质前体细胞的移植克隆细胞系在移植到少突胶质细胞和星形胶质细胞均缺失的病理环境后,如何分化为星形胶质细胞以及少突胶质细胞,从而展现出在体外可证明的双潜能性,但在发育过程中却不会表现出来。最后,描述了一系列研究(使用少突胶质前体细胞系CG4作为模型),这些研究考察了移植的少突胶质前体细胞的迁移行为。这些研究表明,CG4细胞移植到正常成年中枢神经系统后无法存活(或迁移)。然而,如果将它们移植到先前已接受40 Gy X射线照射的中枢神经系统组织中,那么移植的CG4细胞就能存活、分裂并远距离迁移。此外,在X射线照射的环境中,迁移的移植CG4细胞能够进入远处的脱髓鞘病灶,并促进其中脱髓鞘轴突的髓鞘再生。这些研究表明,尽管正常成年中枢神经系统似乎不支持CG4细胞系的存活和迁移,但有可能通过某种方式操纵环境,从而克服环境的这些非允许特性。