Yang Lifeng, Dai Fan, Tang Lian, Le Yulan, Yao Wenjuan
School of Pharmacy, Nantong University, China.
J Toxicol Sci. 2017;42(6):763-771. doi: 10.2131/jts.42.763.
In order to investigate the effects of RhoA/ROCK signaling in macrophage differentiation, 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 μM) for 30 min 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.
为了研究RhoA/ROCK信号在巨噬细胞分化中的作用,我们使用100 ng/mL佛波酯(PMA)在体外诱导U937细胞分化为巨噬细胞。通过观察细胞形态以及检测CD68和清道夫受体A(SR-A)的表达来确认PMA诱导的分化。蛋白质免疫印迹分析显示,PMA处理后,ROCK1和ROCK2的表达以及肌球蛋白磷酸酶靶向亚基1(MYPT1)的磷酸化显著增加。下拉实验表明,用PMA处理U937细胞时,RhoA的激活明显增强。为了进一步证明RhoA/ROCK信号是否能介导PMA诱导的巨噬细胞分化,我们分别在U937细胞中通过小干扰RNA(siRNA)技术成功抑制了RhoA、ROCK1和ROCK2的表达。在PMA诱导的U937细胞中,抑制RhoA、ROCK1或ROCK2可显著抑制巨噬细胞分化以及CD68和SR-A的表达,这表明PMA诱导的巨噬细胞分化与RhoA/ROCK信号通路有关。此外,我们用Y27632(ROCK抑制剂,20 μM)预处理U937细胞30分钟,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诱导的分化以及CD68和SR-A的表达。总之,RhoA/ROCK信号的激活介导了PMA诱导的巨噬细胞分化。