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Multimodal Enhancement of Remyelination by Exercise with a Pivotal Role for Oligodendroglial PGC1α

机译:多模式增强运动并具有枢轴作用的少突胶质PGC1α重新髓鞘形成。

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Summary Remyelination is a multistep regenerative process that results in the reformation of myelin sheaths around demyelinated axons and is a critical therapeutic target. Here we show that immediate access to a running wheel following toxin-induced demyelination in mice enhances oligodendrogenesis, the rate of remyelination, and the proportion of remyelinated axons. RNA sequencing suggests broad activation of?pro-remyelination pathways including phagocytosis by exercise and highlights peroxisome proliferator-activated receptor gamma co-activator 1-alpha (PGC1α) activation. By immunohistochemistry and cell type-specific conditional deletion, we confirmed PGC1α within oligodendrocytes as a transiently expressed factor required for the rate of myelin thickening by exercise. We validated the exercise-enhanced clearance of inhibitory lipid debris from?lesions. Finally, exercise works in parallel with the remyelinating medication clemastine to produce complete remyelination of lesions. Our study demonstrates physical activity as an integrative means to enhance remyelination and details a multimodal mechanism including the pivotal PGC1α-dependent enhancement of myelin thickness.
机译:总结髓鞘再生是一个多步骤的再生过程,可导致脱髓鞘轴突周围髓鞘的再形成,并且是关键的治疗靶点。在这里,我们显示在毒素诱导的小鼠脱髓鞘后,立即进入运转的轮子会增强少突胶质生成,髓鞘再生的速率以及髓鞘再生的比例。 RNA测序表明广泛的β-髓鞘再生途径的激活,包括通过运动吞噬作用,并突出了过氧化物酶体增殖物激活的受体γ共激活物1-α(PGC1α)的激活。通过免疫组织化学和特定于细胞类型的条件缺失,我们证实少突胶质细胞内的PGC1α是运动引起的髓磷脂增厚速率所需的瞬时表达因子。我们验证了运动增强清除病灶抑制性脂质碎片的能力。最后,运动与髓鞘再生药物clemastine并行进行,以使病变完全髓鞘再生。我们的研究表明,体育锻炼是增强髓鞘再生的一种综合手段,并详细介绍了一种多模态机制,包括依赖于PGC1α的髓鞘厚度依赖性增强。

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