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首页> 外文期刊>Neural regeneration research >The Rho-associated kinase inhibitors Y27632 and fasudil promote microglial migration in the spinal cord via the ERK signaling pathway
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The Rho-associated kinase inhibitors Y27632 and fasudil promote microglial migration in the spinal cord via the ERK signaling pathway

机译:RHO相关激酶抑制剂Y27632和Fasudil通过ERK信号通路促进脊髓中的微胶质迁移

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Rho-associated kinase (ROCK) is a key regulatory protein involved in inflammatory secretion in microglia in the central nervous system. Our previous studies showed that ROCK inhibition enhances phagocytic activity in microglia through the extracellular signal-regulated kinase (ERK) signaling pathway, but its effect on microglial migration was unknown. Therefore, in this study, we investigated the effects of the ROCK inhibitors Y27632 and fasudil on the migratory activity of primary cultured microglia isolated from the spinal cord, and we examined the underlying mechanisms. The microglia were treated with Y27632, fasudil and/or the ERK inhibitor U0126. Cellular morphology was observed by immunofluorescence. Transwell chambers were used to assess cell migration. ERK levels were measured by in-cell western blot assay. Y27632 and fasudil increased microglial migration, and the microglia were irregularly shaped and had many small processes. These inhibitors also upregulated the levels of phosphorylated ERK protein. The ERK inhibitor U0126 suppressed these effects of Y27632 and fasudil. These findings suggest that the ROCK inhibitors Y27632 and fasudil promote microglial migration in the spinal cord through the ERK signaling pathway.
机译:RHO相关激酶(岩)是中枢神经系统中的小凝血性炎症分泌的关键调节蛋白。我们以前的研究表明,岩石抑制通过细胞外信号调节激酶(ERK)信号通路增强了小胶质细胞中的吞噬活性,但其对小胶质迁移的影响是未知的。因此,在本研究中,我们研究了岩抑制剂Y27632和Fasudil对从脊髓中分离的原发性培养的微胶质的迁移活性的影响,我们检查了潜在的机制。用Y27632,Fasudil和/或ERK抑制剂U0126处理微胶质细胞。通过免疫荧光观察细胞形态。 Transwell Chambers用于评估细胞迁移。通过细胞内印迹测定法测量ERK水平。 Y27632和Fasudil增加了显微胶质型迁移,并且微胶质细胞不规则地形状并且具有许多小的过程。这些抑制剂还上调了磷酸化ERK蛋白的水平。 ERK抑制剂U0126抑制了Y27632和Fasudil的这些效果。这些发现表明,岩石抑制剂Y27632和Fasudil通过ERK信号通路促进脊髓中的微胶质迁移。

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