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通过移植有丝分裂后少突胶质细胞非常有限的髓鞘再生潜能所进行的证明。

The demonstration by transplantation of the very restricted remyelinating potential of post-mitotic oligodendrocytes.

作者信息

Crang A J, Gilson J, Blakemore W F

机构信息

MRC Cambridge Centre for Brain Repair and Department of Clinical Veterinary Medicine, UK.

出版信息

J Neurocytol. 1998;27(7):541-53. doi: 10.1023/a:1006960032023.

DOI:10.1023/a:1006960032023
PMID:11246493
Abstract

To examine the remyelinating ability of post-mitotic oligodendrocytes, we subjected cell preparations derived from neonatal and adult rats to 40 Grays of X-irradiation to remove mitotically active cells and injected them into areas of demyelination in which the inherent ability to generate remyelinating cells had been inhibited. The extensive remyelination seen following implantation of non-irradiated neonatal and adult cells was almost completely abolished when the transplanted cell suspension was exposed to 40 Grays of X-irradiation, demonstrating that effective remyelination requires the generation of cells by mitosis. Radiation-resistant and therefore non-dividing oligodendrocytes were detected in areas of demyelination following transplantation of neonatal cultures and oligodendrocyte preparations derived from the adult nervous system. However, the pattern of myelin formation associated with the radiation-resistant oligodendrocytes from the two sources was different. Following implantation of X-irradiated neonatal cultures, a small number of oligodendrocytes could be found within the area of demyelination, and although these cells formed sheets of myelin membrane, they did not form myelin sheaths. After implantation of X-irradiated adult cells, in addition to the aberrant myelin formation seen with the neonatal cells, some myelin sheaths were observed. Our findings confirm that effective remyelination requires cell division and suggest that there may be diverse populations of radiation-resistant oligodendrocytes in the adult nervous system, some of which can form myelin sheaths and others of which can only make myelin sheets. Important for the interpretation of our previous studies is the demonstration here that 40 Grays of X-irradiation per se does not inhibit oligodendrocytes from remyelinating axons.

摘要

为了检测有丝分裂后少突胶质细胞的髓鞘再生能力,我们对新生大鼠和成年大鼠的细胞制剂进行40戈瑞的X射线照射,以去除有丝分裂活跃的细胞,然后将其注射到髓鞘脱失区域,该区域内生成髓鞘再生细胞的固有能力已被抑制。当移植的细胞悬液接受40戈瑞的X射线照射时,移植未照射的新生和成年细胞后出现的广泛髓鞘再生几乎完全消失,这表明有效的髓鞘再生需要通过有丝分裂产生细胞。在移植新生大鼠培养物和源自成年神经系统的少突胶质细胞制剂后,在髓鞘脱失区域检测到抗辐射且因此不分裂的少突胶质细胞。然而,来自这两种来源的抗辐射少突胶质细胞相关的髓鞘形成模式有所不同。移植经X射线照射的新生大鼠培养物后,在髓鞘脱失区域内可发现少量少突胶质细胞,尽管这些细胞形成了髓鞘膜片,但并未形成髓鞘。移植经X射线照射的成年细胞后,除了观察到与新生细胞相同的异常髓鞘形成外,还观察到了一些髓鞘。我们的研究结果证实有效的髓鞘再生需要细胞分裂,并表明成年神经系统中可能存在不同群体的抗辐射少突胶质细胞,其中一些能够形成髓鞘,而另一些只能形成髓鞘膜片。对我们之前研究的解释很重要的一点是,此处证明了40戈瑞的X射线照射本身并不抑制少突胶质细胞对轴突进行髓鞘再生。

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