Blakemore W F
Department of Clinical Veterinary Medicine, University of Cambridge.
Neuropathol Appl Neurobiol. 1992 Oct;18(5):460-6. doi: 10.1111/j.1365-2990.1992.tb00812.x.
Transplantation of different glial cells into areas of demyelination made in the adult rat spinal cord allows insights into the cell-cell interaction necessary to reconstruct a glial environment around demyelinated axons. Such studies have shown that type-1 astrocytes are central to the exclusion of Schwann cells from areas of glia-free demyelination. However, for these cells to be established in a manner which prevents Schwann cell remyelination of CNS axons, cells of the O-2A lineage are also required. If cultures of isogeneic rat type-1 astrocytes and mouse O-2A cells are transplanted into lesions made in non-immunosuppressed animals. Schwann cell remyelination is limited and extensive oligodendrocyte remyelination is achieved. This paradigm creates a model of immune mediated demyelination in which the immune response is not primarily directed at oligodendrocyte specific epitopes.
将不同的神经胶质细胞移植到成年大鼠脊髓中制造的脱髓鞘区域,有助于深入了解在脱髓鞘轴突周围重建神经胶质环境所需的细胞间相互作用。此类研究表明,1型星形胶质细胞对于施万细胞从无胶质细胞的脱髓鞘区域的排除至关重要。然而,为了以防止中枢神经系统轴突施万细胞再髓鞘化的方式建立这些细胞,还需要少突胶质前体细胞系的细胞。如果将同基因大鼠1型星形胶质细胞和小鼠少突胶质前体细胞系的细胞培养物移植到未免疫抑制动物制造的损伤部位,施万细胞的再髓鞘化会受到限制,并且会实现广泛的少突胶质细胞再髓鞘化。这种模式创建了一种免疫介导的脱髓鞘模型,其中免疫反应并非主要针对少突胶质细胞特异性表位。