京尼平调控NLRP3通路致HK-2细胞毒性作用机制研究

    Study of the Mechanism of Genipin Induced Cytotoxicity on HK-2 Cell via NLRP3 Pathway

    • 摘要:
      目的  基于NLRP3通路探讨京尼平(genipin,GP)对人源肾小管上皮细胞(human tubular epithelial cells,HK-2)毒性作用。
      方法 CCK8法筛选GP致HK-2细胞毒性浓度及作用时间;Western blotting检测肾损伤标志物Kim-1、OPN及NLRP3通路蛋白NLRP3、Caspase-1、IL-1β、IL-18表达;研究GP对HK-2细胞的毒性作用,并采用Hoechst/PI染色法检测HK-2细胞凋亡,DCFH-DA法检测HK-2细胞中ROS水平,高内涵成像检测线粒体膜电位(mitochondrial membrane potential,MMP)和Ca2+水平,Western blotting和qPCR法检测Kim-1、OPN、NLRP3、Caspase-1、IL-1β、IL-18蛋白及其mRNA表达水平,研究NLRP3抑制剂格列苯脲对GP毒性的拮抗作用及其机制。
      结果 GP对HK-2细胞在12、24、48 h的IC50分别为433.00、110.50、72.99 μg·mL–1;与空白组相比,GP处理后HK-2细胞PI阳性率、ROS、Ca2+水平显著增加,MMP显著下降,Kim-1、OPN、IL-1β、IL-18、NLRP3、Caspase-1蛋白及mRNA水平均显著升高(P<0.05,P<0.01);NLRP3通路抑制剂格列苯脲可以明显改善GP细胞毒性作用及相关分子变化。
      结论 GP可能通过激活NLRP3通路诱导HK-2细胞损伤,抑制NLRP3通路可减轻GP诱导的HK-2细胞炎症损伤。

       

      Abstract:
      OBJECTIVE  To investigate the toxicity of genipin on human tubular epithelial cells(HK-2) based on NLRP3 pathway.
      METHODS  The cytotoxic concentration and action time of genipin on HK-2 were detected by CCK8. The Western blotting was used to detect the expression of Kim-1, OPN and NLRP3 pathway protein NLRP3, Caspase-1, IL-1β and IL-18. Studied on the toxic effects of genipin on HK-2 cells, apoptosis in HK-2 cell was detected by Hoechst/PI staining, and the level of ROS in HK-2 cell was detected by DCFH-DA. High-content imaging techniques was used to detect mitochondrial membrane potential(MMP) and Ca2+ levels, Western blotting and qPCR methods was used to detect the expression levels of Kim-1, OPN, NLRP3, Caspase-1, IL-1β, IL-18 protein and mRNA. To study the antagonistic effect of NLRP3 inhibitor glyburide on GP toxicity and its mechanism.
      RESULTS The IC50 values of genipin for HK-2 cell were 433.00, 110.50 and 72.99 μg·mL–1 at 12, 24 and 48 h, respectively. Compared with the blank group, after the treatment of genipin, the positive rate of PI, ROS, Ca2+ levels of HK-2 cell increased significantly, MMP decreased significantly, and the levels of Kim-1, OPN, IL-1β, IL-18, NLRP3, Caspase-1 protein and mRNA were significantly increased(P<0.05, P<0.01), and the NLRP3 pathway inhibitor glyburide could significantly improve the cytotoxic effects of genipin and related molecular changes.
      CONCLUSION Genipin might have cytotoxicity on HK-2 cells via NLRP3 pathway, and inhibiting NLRP3 pathway can improve the inflammation caused by genipin induced cytotoxicity on HK-2 cells.

       

    /

    返回文章
    返回