首页> 美国卫生研究院文献>The Journal of Neuroscience >R-Ras1 and R-Ras2 Are Essential for Oligodendrocyte Differentiation and Survival for Correct Myelination in the Central Nervous System
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R-Ras1 and R-Ras2 Are Essential for Oligodendrocyte Differentiation and Survival for Correct Myelination in the Central Nervous System

机译:R-Ras1和R-Ras2对于少突胶质细胞的分化和中枢神经系统正确的髓鞘存活是必不可少的。

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摘要

Rapid and effective neural transmission of information requires correct axonal myelination. Modifications in myelination alter axonal capacity to transmit electric impulses and enable pathological conditions. In the CNS, oligodendrocytes (OLs) myelinate axons, a complex process involving various cellular interactions. However, we know little about the mechanisms that orchestrate correct myelination. Here, we demonstrate that OLs express R-Ras1 and R-Ras2. Using female and male mutant mice to delete these proteins, we found that activation of the PI3K/Akt and Erk1/2-MAPK pathways was weaker in mice lacking one or both of these GTPases, suggesting that both proteins coordinate the activity of these two pathways. Loss of R-Ras1 and/or R-Ras2 diminishes the number of OLs in major myelinated CNS tracts and increases the proportion of immature OLs. In R-Ras1−/− and R-Ras2−/−-null mice, OLs show aberrant morphologies and fail to differentiate correctly into myelin-forming phenotypes. The smaller OL population and abnormal OL maturation induce severe hypomyelination, with shorter nodes of Ranvier in R-Ras1−/− and/or R-Ras2−/− mice. These defects explain the slower conduction velocity of myelinated axons that we observed in the absence of R-Ras1 and R-Ras2. Together, these results suggest that R-Ras1 and R-Ras2 are upstream elements that regulate the survival and differentiation of progenitors into OLs through the PI3K/Akt and Erk1/2-MAPK pathways for proper myelination.>SIGNIFICANCE STATEMENT In this study, we show that R-Ras1 and R-Ras2 play essential roles in regulating myelination in vivo and control fundamental aspects of oligodendrocyte (OL) survival and differentiation through synergistic activation of PI3K/Akt and Erk1/2-MAPK signaling. Mice lacking R-Ras1 and/or R-Ras2 show a diminished OL population with a higher proportion of immature OLs, explaining the observed hypomyelination in main CNS tracts. In vivo electrophysiology recordings demonstrate a slower conduction velocity of nerve impulses in the absence of R-Ras1 and R-Ras2. Therefore, R-Ras1 and R-Ras2 are essential for proper axonal myelination and accurate neural transmission.
机译:快速有效的信息神经传递需要正确的轴突髓鞘形成。髓鞘化的改变会改变轴突的能力,以传递电脉冲并引起病理状况。在中枢神经系统中,少突胶质细胞(OLs)髓鞘轴突是一个复杂的过程,涉及各种细胞相互作用。但是,我们对协调正确的髓鞘形成的机制知之甚少。在这里,我们证明OLs表达R-Ras1和R-Ras2。使用雌性和雄性突变小鼠删除这些蛋白,我们发现在缺乏一个或两个这些GTPases的小鼠中,PI3K / Akt和Erk1 / 2-MAPK途径的激活较弱,这表明这两种蛋白均能协调这两个途径的活性。 R-Ras1和/或R-Ras2的丢失减少了主要有髓CNS区域中OL的数量,并增加了未成熟OL的比例。在R-Ras1 -/-和R-Ras2 -/- -null小鼠中,OL显示异常的形态,并且无法正确区分为形成髓鞘的表型。较小的OL种群和异常的OL成熟会导致严重的髓鞘减少,在R-Ras1 -/-和/或R-Ras2 -/-小鼠中,Ranvier的结节较短。这些缺陷解释了我们在没有R-Ras1和R-Ras2的情况下观察到的髓鞘轴突的传导速度较慢。总之,这些结果表明,R-Ras1和R-Ras2是上游细胞,它们通过PI3K / Akt和Erk1 / 2-MAPK途径调节祖细胞向OL的存活和分化,以实现适当的髓鞘形成。>意义声明 >在这项研究中,我们显示R-Ras1和R-Ras2在体内通过调节PI3K / Akt和Erk1 / 2-MAPK信号的协同激活,在调节髓鞘形成和控制少突胶质细胞(OL)生存和分化的基本方面起着至关重要的作用。缺乏R-Ras1和/或R-Ras2的小鼠的OL种群减少,未成熟OL的比例更高,这解释了在主要CNS道中观察到的髓鞘减少。体内电生理学记录表明,在没有R-Ras1和R-Ras2的情况下,神经冲动的传导速度较慢。因此,R-Ras1和R-Ras2对于正确的轴突髓鞘形成和准确的神经传递至关重要。

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