摘要
目的 观察红细胞生成素(EPO)对补体成分C3片段C3a介导的肾小管上皮细胞间充质转分化(EMT)的影响.方法 将人近端肾小管上皮细胞(HK-2)分为6组:对照组、EPO组、TGF-β组、TGF-β+EPO组、C3a组、EPO+C3a组,分别用RT-PCR、Western印迹和细胞免疫荧光方法检测HK-2细胞α-SMA、E-cadherin、C3的mRNA和蛋白表达.结果 与对照组和EPO组比较,C3a或TGF-β干预HK2细胞后,αt-SMA mRNA和蛋白表达增强(均P<0.05),E-cadherin mRNA和蛋白表达减少(均P< 0.05),补体C3 mRNA和蛋白表达增强(均P< 0.05);而同时给予EPO干预后,C3a或TGF-β的上述作用可被明显减弱(均P<0.05).结论 EPO可抑制C3a介导的肾小管上皮细胞EMT.
Objective To investigate the effects of erythropoietin (EPO) on complement 3a (C3a)-induced renal tubular epithelial to mesenchymal transition. Methods The HK-2 cells were divided into 6 groups namely control group,EPO group,TGF-β group,TGF-β+EPO group,C3a group and EPO+C3a group.The mRNA and protein expressions of α-SMA,E-cadherin and C3 were investigated by RT-PCR,Western blot and immunofluorescence respectively. Results Compared with control group and EPO group,the mRNA and protein expressions of α-SMA in HK-2 cells were up-regulated after the intervention of C3a or TGF-β (all P〈0.05).On the contrast,the mRNA and protein expressions of E-cadherin were down-regulated(P〈0.05),the mRNA and protein expressions of C3 were enhanced (all P〈0.05).However,all those above effects of C3a or TGF-β were inhibited after the intervention of EPO (all P〈0.05). Conclusion EPO is capable of suppressing the epithelial to mesenchymal transition induced by C3a.
出处
《中华肾脏病杂志》
CAS
CSCD
北大核心
2012年第2期115-120,共6页
Chinese Journal of Nephrology
基金
基金项目:福建省卫生厅青年科研基金(2008-2-23)