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SAA1在狼疮小鼠肾脏中的表达及其对小鼠肾小管上皮细胞EMT的作用 被引量:2

Expression of SAA1 in kidney of lupus mice and its effect on EMT of mRTECs
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摘要 目的:探讨SAA1在狼疮小鼠肾脏中的表达及其对肾脏纤维化的影响。方法:选取自发性狼疮肾炎小鼠(LN小鼠)与阴性对照的C57/BL小鼠用于体内实验,应用Masson染色检测其肾脏组织纤维化程度,应用Real-time PCR、Western blot和免疫组化技术检测组织中SAA1以及相关EMT指标的表达情况;体外实验中,将mRTEC细胞应用不同处理后,分为空白对照组、LPS处理组、LPS+Si-NC和LPS+Si-SAA1组,应用Western blot和免疫细胞荧光检测相关蛋白表达。结果:LN小鼠肾脏发生明显纤维化,SAA1表达较正常组明显升高;LPS能诱导mRTECs中SAA1、FN和α-SMA的表达,并降低E-Ca蛋白水平,而同时沉默SAA1能有效减缓LPS这一作用。结论:SAA1在狼疮小鼠中表达明显升高,且能促进肾小管上皮细胞的EMT进程。 Objective:To investigate the expression of SAA1 in the kidney of lupus mice and its effect on renal fibrosis.Methods: Spontaneous lupus nephritis mice(LN mice) and C57/BL mice(negative control mice) were selected in vivo experiment.Masson staining was used to detect the degree of renal fibrosis.Real-time PCR,Western blot and immunohistochemical techniques were used to detect the expression of SAA1 and related EMT in tissues.MRTEC cells were divided into blank control group,LPS treatment group,LPS+Si-NC group and LPS+Si-SAA1 group after different treatments.Western blot and immunofluorescence were used to detect the expression of related proteins.Results: LN mice had obvious renal fibrosis,and the expression of SAA1 was significantly higher than that of the normal group.LPS could induce the expression of SAA1,FN and alpha-SMA in mRTECs,and reduce the level of E-Ca protein,while silencing SAA1 could effectively alleviate the effect of LPS.Conclusion: SAA1 expression in lupus mice is significantly increased and can promote the EMT process of renal tubular epithelial cells.
作者 周星丞 张帆 严瑞 潘秀超 余洁 潘洪奖 田平平 刘忠强 石明隽 郭兵 ZHOU Xing-Cheng;ZHANG Fan;YAN Rui;PAN Xiu-Chao;YU Jie;PAN Hong-Jiang;TIAN Ping-Ping;LIU Zhong-Qiang;SHI Ming-Jun;GUO Bing(Department of Pathophysiology,Guizhou Medical University,Guiyang 550025,China)
出处 《中国免疫学杂志》 CAS CSCD 北大核心 2019年第21期2561-2565,2575,共6页 Chinese Journal of Immunology
基金 贵州省科技厅基础研究计划项目(黔科合基础[2019]1272号) 贵州省科技厅学术新苗项目(黔科合平台人才[2017]5718-20) 贵阳市科技计划项目(筑科合同[2017]30-23号)
关键词 狼疮肾炎 EMT mRTEC细胞 SAA1 Lupus nephritis EMT mRTEC cells SAA1
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