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Macrophage differentiation induced by PMA is mediated by activation of RhoA/ROCK signaling

机译:PMA诱导的巨噬细胞分化是通过RHOO /摇滚信令的激活介导的

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In order to investigate the effects of RhoA/ROCK signaling in macrophage differentia-. tion, we used 100 ng/mL PMA to induce macrophage differentiation from U937 cells in vitro. The observation of cell morphology and the expression of CD68 and SR-A were performed to confirm the differentiation induced by PMA. Western blot analysis showed that the expression of ROCK1 and ROCK2 and the phosphorylation of MYPT1 were significantly increased after PMA treatment. Pulldown assay showed that the activation of RhoA was obviously enhanced when U937 cells were treated with PMA. In order to further demonstrate whether RhoA/ROCK signaling could mediate the macrophage differentiation induced by PMA, we successfully suppressed the expression of RhoA, ROCK1 and ROCK2 by performing siRNA technology in U937 cells, respectively. The macrophage differentiation and the expression of CD68 and SR-A were significantly inhibited by the suppression of RhoA, ROCK1 or ROCK2 in PMA-induced U937 cells, indicating that the macrophage differentiation induced by PMA is associated with RhoA/ROCK signaling pathway. In addition, we pretreated U937 cells with Y27632 (ROCK inhibitor, 20 mu M) for 30 mm and then observed the macrophage differentiation induced by PMA. The result illustrated that Y27632 pretreatment obviously inhibited PMA-induced differentiation and the expression of CD68 and SR-A. In conclusion, the activation of RhoA/ROCK signaling is responsible for the macrophage differentiation induced by PMA.
机译:为了探讨RhoA /摇滚信令在巨噬细胞不同的影响。 Tion,我们使用100ng / ml pma在体外诱导来自U937细胞的巨噬细胞分化。进行细胞形态的观察和CD68和SR-A的表达,以确认PMA诱导的分化。 Western印迹分析表明,PMA处理后,Rock1和Rock2的表达和Mypt1的磷酸化显着增加。下拉测定表明,当用PMA处理U937细胞时,无菌的活化明显增强。为了进一步证明RHOA /摇滚信令是否可以介导PMA诱导的巨噬细胞分化,我们通过分别在U937细胞中进行siRNA技术成功地抑制了RHOA,ROCK1和ROCK2的表达。通过PMA诱导的U937细胞中的RhOA,Rock1或Rock2抑制CD68和Sr-A的巨噬细胞分化和表达,表明PMA诱导的巨噬细胞分化与RHOA /岩石信号通路相关。此外,我们用Y27632(岩石抑制剂,20μm)预处理U937细胞30mm,然后观察PMA诱导的巨噬细胞分化。结果表明,Y27632预处理明显抑制了PMA诱导的分化和CD68和SR-A的表达。总之,rhOA /岩石信号传导的激活是PMA诱导的巨噬细胞分化的原因。

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