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运动通过少突胶质细胞 PGC1α 发挥关键作用增强髓鞘再生的多模态增强作用。

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

机构信息

Hotchkiss Brain Institute and the Department of Clinical Neurosciences University of Calgary, Calgary, AB, Canada.

Department of Biology, University of Lethbridge, Lethbridge, AB, Canada.

出版信息

Cell Rep. 2018 Sep 18;24(12):3167-3179. doi: 10.1016/j.celrep.2018.08.060.

Abstract

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.

摘要

髓鞘再生是一个多步骤的再生过程,导致脱髓鞘轴突周围的髓鞘重新形成,是一个关键的治疗靶点。在这里,我们表明,在小鼠毒素诱导脱髓鞘后立即使用跑步机,可增强少突胶质细胞生成、髓鞘再生速度和髓鞘再生轴突的比例。RNA 测序表明,运动广泛激活了促髓鞘再生途径,包括吞噬作用,并突出了过氧化物酶体增殖物激活受体γ共激活因子 1-α(PGC1α)的激活。通过免疫组织化学和细胞类型特异性条件性缺失,我们证实了 PGC1α 在少突胶质细胞内作为一个短暂表达的因子,是运动增加髓鞘增厚速度所必需的。我们验证了运动增强了对病变中抑制性脂质碎片的清除。最后,运动与髓鞘再形成药物克来司汀平行作用,使病变完全髓鞘再生。我们的研究表明,体育活动是增强髓鞘再生的一种综合手段,并详细描述了一种多模式机制,包括关键的 PGC1α 依赖性增强髓鞘厚度。

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