机构地区:[1]昆明医科大学第一附属医院泌尿外科,650032
出 处:《天津医药》2024年第3期250-255,共6页Tianjin Medical Journal
基 金:云南省科技厅科技计划项目(202001AY070001-158)。
摘 要:目的探究人肾皮质近曲小管上皮细胞(HK-2)经Ca^(2+)作用后的焦亡经典通路激活及黏附性变化对含钙肾结石形成的作用及机制。方法不同质量浓度的CaCl2(0、0.1、0.5、1.0、2.0、4.0、8.0 g/L)培养HK-2细胞24 h,使用细胞计数试剂盒(CCK-8)及流式细胞凋亡术检测筛选最佳处理浓度。使用透射电镜观察高钙环境下肾小管上皮细胞微结构的变化。在高钙处理后用2,7-二氯荧光素二乙酸酯(DCFH-DA)检测细胞内活性氧(ROS)的产生,并采用实时荧光定量聚合酶链式反应和Western blot法分别检测高钙刺激后HK-2细胞焦亡相关NOD样受体热蛋白结构域相关蛋白3(NLRP3)、胱天蛋白酶1(Caspase-1)、gasderminD(GSDMD)和黏附分子骨桥蛋白(OPN)、CD44的mRNA和蛋白表达水平变化,酶联免疫吸附试验检测白细胞介素(IL)-1β、IL-18和黏附分子单核细胞趋化蛋白1(MCP-1)在高钙刺激后的表达变化。结果Ca^(2+)对HK-2细胞生长具有细胞毒性并且可以促进其凋亡,Ca^(2+)浓度越高,对HK-2细胞生长的毒性越大且凋亡率越高。高钙可以促进HK-2细胞发生细胞膜完整性缺失、内容物释放及胞内大量空泡产生等焦亡样形态学改变。与对照组相比,1.0 g/L及2.0 g/L CaCl2组的ROS表达水平依次升高,焦亡相关基因NLRP3、Caspase-1、GSDMD、IL-1β、IL-18以及黏附相关基因OPN、CD44、MCP-1的mRNA和蛋白表达水平均依次升高(P<0.05)。结论高钙能使HK-2细胞发生氧化应激损伤并产生ROS,从而激活NLRP3炎症小体,进而导致细胞焦亡经典通路的激活和细胞黏附性的增加,最终间接促进肾结石的形成。Objective To investigate the possible role and mechanism of activation of pyroptosis classical pathway and alterations in cell adhesion in calcium-containing kidney stones after the action of high concentration of Ca^(2+)on HK-2 cells.Methods HK-2 cells were cultured in the presence of different concentrations of CaCl2(0,0.1,0.5,1.0,2.0,4.0 and 8.0 g/L)for 24 hours,and cell counting Kit-8(CCK-8)and flow cytometry were used to determine the optimal treatment concentration.Subsequently,the ultrastructure of renal tubular epithelial cells under high Ca^(2+)condition was observed by transmission electron microscopy after Ca^(2+)treatment.DCFH-DA staining was used to detect intracellular reactive oxygen species production,and quantitative real-time polymerase chain reaction(qRT-PCR)and Western blot analysis were performed to examine the expression of pyroptosis-related proteins NLRP3,Caspase-1,gasdermin D(GSDMD),adhesive molecules osteopontin(OPN)and CD44 at mRNA and protein levels after high concentration Ca^(2+)treatment.The expression levels of pyroptosis-related inflammatory factors interleukin(IL)-1β,IL-18 and adhesive molecule monocyte chemotactic protein-1(MCP-1)were detected by enzyme-linked immunosorbent assay(ELISA)after high Ca^(2+)stimulation.Results Ca^(2+)showed cytotoxicity for HK-2 cell growth and can promote apoptosis.The higher the Ca^(2+)concentration,the more toxicity and apoptosis rate for HK-2 cell growth.High concentration of Ca^(2+)can promote pyroptosis-like morphological changes in HK-2 cells,including loss of cell membrane integrity,release of contents and numerous intracellular vacuoles.Compared with the control group,the expression levels of ROS were sequentially increased in the 1.0 g/L CaCl2 group and the 2.0 g/L CaCl2 group,and the expression levels of pyroptosis-related genes NLRP3,Caspase-1,GSDMD,and the pyroptosis-associated inflammatory factors IL-1βand IL-18,as well as the adhesion molecules OPN,CD44 and MCP-1 were significantly increased(P<0.05).Conclusion High Ca^(2+)treatment
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...