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Insulin-Like Growth Factor (IGF) Signaling through Type 1 IGF Receptor Plays an Important Role in Remyelination

机译:通过1型IGF受体的胰岛素样生长因子(IGF)信号在髓鞘再生中起重要作用

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摘要

We examined the role of IGF signaling in the remyelination process by disrupting the gene encoding the type 1 IGF receptor (IGF1R) specifically in the mouse brain by Cre-mediated recombination and then exposing these mutants and normal siblings to cuprizone. This neurotoxicant induces a demyelinating lesion in the corpus callosum that is reversible on termination of the insult. Acute demyelination and oligodendrocyte depletion were the same in mutants and controls, but the mutants did not remyelinate adequately. We observed that oligodendrocyte progenitors did not accumulate, proliferate, or survive within the mutant mice, compared with wild type, indicating that signaling through the IGF1R plays a critical role in remyelination via effects on oligodendrocyte progenitors.
机译:我们通过Cre介导的重组破坏小鼠脑中编码1型IGF受体(IGF1R)的基因,然后将这些突变体和正常同胞暴露于铜酮,从而检查了IGF信号在髓鞘再生过程中的作用。这种神经毒剂会导致call体脱髓鞘病变,这种损伤在损伤终止后是可逆的。突变和对照中的急性脱髓鞘和少突胶质细胞耗竭是相同的,但是突变体不能充分地使髓鞘再生。我们观察到,与野生型相比,少突胶质细胞祖细胞没有在突变小鼠中积累,增殖或存活,这表明通过IGF1R的信号传导通过对少突胶质细胞祖细胞的作用在髓鞘再生中起关键作用。

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