Baron-Van Evercooren A, Avellana-Adalid V, Ben Younes-Chennoufi A, Gansmuller A, Nait-Oumesmar B, Vignais L
INSERM, Laboratorie de Neurobiologie Cellularie, Moleculaire et Clinique, Hopital de la Salperiere, Paris, France.
Glia. 1996 Feb;16(2):147-64. doi: 10.1002/(SICI)1098-1136(199602)16:2<147::AID-GLIA7>3.0.CO;2-0.
In the present paper, Dil-labeled myelin-forming cells were traced after their transplantation at a distance from a lysolecithin induced lesion in the adult wild-type and shiverer mouse spinal cord. Optical and ultrastructural observations indicate that after their transplantation, Dil-labeled Schwann cells and oligodendrocyte progenitors were found at the level of the graft as well as at the level of the lesion thus confirming that myelin-forming cells were able to migrate in the adult lesioned CNS (Gout et al., Neurosci Lett 87:195-199, 1988). Between the graft and the lesion, labeled Schwann cells and oligodendrocyte progenitors were absent in the gray matter, but were found as previously described, in specific locations (Baron-Van Evercooren et al., J Neurosci Res 35:428-438, 1993; Vignais et al., J Dev Neurosci 11:603-612, 1993). Both cell types were found along blood vessel walls and more precisely in the Virchow-Robin perivascular spaces. They were identified in the meninges among meningeal cells, collagen fibers, or occasionally in direct contact with the basement membrane forming the glia limitans. In addition to these findings, three major observations were made. In the ependymal region, myelin-forming cells were localized between or at the basal pole of ependymocytes. While Dil-labeled oligodendrocyte progenitors were noted to migrate along the outer surface of myelin sheats in CNS wild-type and shiverer white matter, Schwann cells were excluded from this structure in the wild-type mouse spinal cord. Moreover, in the shiverer mouse, migrating Schwann cells did not seem to interact directly with myelin sheats nor with mature oligodendrocytes. Finally, both cell types were seen to invade extensively the spinal peripheral roots. Our ultrastructural observations clearly suggest that multiple cell-cell and cell-substrate interactions rule the migration of myelin-forming cells in the adult CNS infering that multiple mechanisms are involved in this process.
在本论文中,对用Dil标记的形成髓鞘细胞进行移植后追踪,移植部位远离成年野生型和颤抖小鼠脊髓中溶血卵磷脂诱导的损伤部位。光学和超微结构观察表明,移植后,在移植部位以及损伤部位均发现了Dil标记的施万细胞和少突胶质前体细胞,从而证实形成髓鞘细胞能够在成年受损中枢神经系统中迁移(Gout等人,《神经科学快报》87:195 - 199,1988年)。在移植部位和损伤部位之间,灰质中未发现标记的施万细胞和少突胶质前体细胞,但如先前所述,在特定位置发现了它们(Baron - Van Evercooren等人,《神经科学研究杂志》35:428 - 438,1993年;Vignais等人,《发育神经科学杂志》11:603 - 612,1993年)。两种细胞类型均沿血管壁发现,更确切地说是在血管周围间隙中发现。在脑膜细胞、胶原纤维之间的脑膜中鉴定出了它们,偶尔也发现它们与形成胶质界膜的基底膜直接接触。除了这些发现外,还进行了三项主要观察。在室管膜区域,形成髓鞘细胞定位于室管膜细胞之间或室管膜细胞的基极处。虽然在中枢神经系统野生型和颤抖小鼠白质中,Dil标记的少突胶质前体细胞沿髓鞘外表面迁移,但在野生型小鼠脊髓中,施万细胞被排除在该结构之外。此外,在颤抖小鼠中,迁移的施万细胞似乎不与髓鞘也不与成熟少突胶质细胞直接相互作用。最后,两种细胞类型均广泛侵入脊髓外周神经根。我们的超微结构观察清楚地表明,多种细胞 - 细胞和细胞 - 基质相互作用决定了成年中枢神经系统中形成髓鞘细胞的迁移,这意味着该过程涉及多种机制。