Hunter James Kelly Research Institute, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY, USA.
Department of Pharmacology and Toxicology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY, USA.
Nat Neurosci. 2020 Oct;23(10):1215-1228. doi: 10.1038/s41593-020-0689-4. Epub 2020 Aug 17.
Axon degeneration is a hallmark of many neurodegenerative disorders. The current assumption is that the decision of injured axons to degenerate is cell-autonomously regulated. Here we show that Schwann cells (SCs), the glia of the peripheral nervous system, protect injured axons by virtue of a dramatic glycolytic upregulation that arises in SCs as an inherent adaptation to axon injury. This glycolytic response, paired with enhanced axon-glia metabolic coupling, supports the survival of axons. The glycolytic shift in SCs is largely driven by the metabolic signaling hub, mammalian target of rapamycin complex 1, and the downstream transcription factors hypoxia-inducible factor 1-alpha and c-Myc, which together promote glycolytic gene expression. The manipulation of glial glycolytic activity through this pathway enabled us to accelerate or delay the degeneration of perturbed axons in acute and subacute rodent axon degeneration models. Thus, we demonstrate a non-cell-autonomous metabolic mechanism that controls the fate of injured axons.
轴突变性是许多神经退行性疾病的标志。目前的假设是,受伤轴突退化的决定是细胞自主调节的。在这里,我们表明,施万细胞(SCs),周围神经系统的神经胶质,通过剧烈的糖酵解上调来保护受伤的轴突,这是SCs对轴突损伤的固有适应。这种糖酵解反应,加上增强的轴突-胶质代谢偶联,支持轴突的存活。SCs 中的糖酵解转变在很大程度上由代谢信号枢纽,雷帕霉素靶蛋白复合物 1 驱动,以及下游转录因子缺氧诱导因子 1-α和 c-Myc,它们共同促进糖酵解基因表达。通过这条途径对神经胶质糖酵解活性的操纵使我们能够加速或延迟急性和亚急性啮齿动物轴突变性模型中受干扰轴突的变性。因此,我们证明了一种非细胞自主的代谢机制,它控制着受伤轴突的命运。