Blakemore William F, Gilson Jennifer M, Crang A John
Department of Clinical Veterinary Medicine, University of Cambridge, Cambridge CB3 OES, UK.
Exp Neurol. 2003 Dec;184(2):955-63. doi: 10.1016/S0014-4886(03)00347-9.
To date, most experiments examining the myelination potential of transplanted cells have been undertaken into either the immature nervous system or into acutely demyelinating lesions. Since these are situations where myelination or remyelination are occurring, such studies provide little information on the likely outcome of introducing myelinogenic cells into area of chronic demyelination. In an attempt to gain a greater understanding of the interaction between astrocytes and oligodendrocyte progenitors in areas of demyelination, we undertook transplantation experiments in which an identical preparation of oligodendrocyte progenitors (OPCs) was (1) transplanted directly into astrocyte-free areas of acute demyelination (3 days after induction), (2) transplanted cranial to similar areas of demyelination (20 days after induction) or (3) transplanted cranial to areas of demyelination (20 days after induction) that had been injected with astrocytes at 3 days to confront OPCs with demyelinated axons in an astrocytic environment. The acute astrocyte-free lesions were remyelinated by oligodendrocytes and Schwann cells while the delayed interaction of OPCs with demyelinating lesions resulted in only oligodendrocyte remyelination, the extent of which was reduced when the area of demyelination contained astrocytes. The results of these experiments illustrate that the introduction of OPCs into an astrocyte-free area of demyelination soon after its induction favours Schwann cell differentiation while the presence of established astrocytes in an area of demyelination has an inhibitory effect on the extent of oligodendrocyte remyelination achieved by OPCs.
迄今为止,大多数检测移植细胞髓鞘形成潜能的实验都是在未成熟神经系统或急性脱髓鞘病变中进行的。由于这些情况是正在发生髓鞘形成或再髓鞘化的情况,此类研究几乎没有提供关于将髓鞘形成细胞引入慢性脱髓鞘区域可能结果的信息。为了更深入了解脱髓鞘区域星形胶质细胞与少突胶质前体细胞之间的相互作用,我们进行了移植实验,在实验中,将相同制备的少突胶质前体细胞(OPCs)(1)直接移植到急性脱髓鞘的无星形胶质细胞区域(诱导后3天),(2)移植到类似脱髓鞘区域的头侧(诱导后20天),或(3)移植到脱髓鞘区域的头侧(诱导后20天),该区域在3天时已注射星形胶质细胞,以使少突胶质前体细胞在星形胶质细胞环境中与脱髓鞘轴突接触。急性无星形胶质细胞病变由少突胶质细胞和施万细胞进行再髓鞘化,而少突胶质前体细胞与脱髓鞘病变的延迟相互作用仅导致少突胶质细胞再髓鞘化,当脱髓鞘区域含有星形胶质细胞时,再髓鞘化程度降低。这些实验结果表明,在脱髓鞘诱导后不久将少突胶质前体细胞引入无星形胶质细胞的脱髓鞘区域有利于施万细胞分化,而脱髓鞘区域中已有的星形胶质细胞的存在对少突胶质前体细胞实现的少突胶质细胞再髓鞘化程度具有抑制作用。