再髓鞘化
少突胶质细胞
转化生长因子
多发性硬化
中枢神经系统
生物
神经科学
再生(生物学)
奥利格2
脱髓鞘病
免疫学
髓鞘
细胞生物学
作者
Maki Hamaguchi,Rieko Muramatsu,Harutoshi Fujimura,Hideki Mochizuki,Hirotoshi Kataoka,Toshio Yamashita
出处
期刊:eLife
[eLife Sciences Publications, Ltd.]
日期:2019-05-09
卷期号:8
被引量:43
摘要
Oligodendrocyte maturation is necessary for functional regeneration in the CNS; however, the mechanisms by which the systemic environment regulates oligodendrocyte maturation is unclear. We found that Transforming growth factor (TGF)-β1, which is present in higher levels in the systemic environment, promotes oligodendrocyte maturation. Oligodendrocyte maturation was enhanced by adult mouse serum treatment via TGF-β type I receptor. Decrease in circulating TGF-β1 level prevented remyelination in the spinal cord after toxin-induced demyelination. TGF-β1 administration promoted remyelination and restored neurological function in a multiple sclerosis animal model. Furthermore, TGF-β1 treatment stimulated human oligodendrocyte maturation. These data provide the therapeutic possibility of TGF-β for demyelinating diseases.
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