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作 者:陈芳[1] 成芳[1] 项倩彤[1] 郭思佳[1] 查晓军[1,2] 王德光[3] 周海胜[1,2]
机构地区:[1]安徽医科大学生物化学与分子生物学教研室,合肥230032 [2]皮肤病学国家重点实验室培育基地,合肥230032 [3]安徽医科大学第二附属医院肾内科,合肥23060
出 处:《安徽医科大学学报》2013年第6期595-600,共6页Acta Universitatis Medicinalis Anhui
基 金:国家自然科学基金(编号:81172591)
摘 要:目的探讨转化生长因子β1(TGF-β1)在人肾小管上皮细胞转分化中的作用,建立肾小管上皮-间质细胞转分化(TEMT)模型。方法实验分为正常对照组和TGF-β1处理组,利用TGF-β1处理人肾小管上皮细胞(HK-2)24 h,分别应用Western blot和免疫荧光方法检测上皮细胞和间质细胞分子标记的表达变化;应用划痕和Transwell assay方法检测细胞迁移及侵袭能力。结果与正常对照组比较,TGF-β1处理组HK-2细胞呈梭形,上皮细胞标记分子E-cadherin表达减弱,差异有统计学意义(P<0.01),间质细胞标记分子骨架蛋白Vimentin和β-catenin表达增强,差异有统计学意义(P<0.01);细胞的迁移及侵袭能力亦明显增强。结论 TGF-β1刺激后HK-2细胞促进上皮细胞转化为间质细胞。Objective To investigate the roles of transforming growth factor β1(TGF-β1) (luring transdifferentiation of human renal tubular epithelial cells, and to establish a model of epithelial-mesenchymal transdifferentiation.Methods Tile experiment was divided into control and experimental groups. Human renal tubular epithelial cells (HK-2) were treated by TGF-β1 for 24 hours. The molecular markers in epithelial or mesenchymal eells were investigated by using Western blot and immune-fluorescence. To determine migration and invasion, scratching test and transwell assay were performed. Results The mesenchymal morphology was exhibited in HK-2 cells treated for 24 h by TGF-β1 (10 ng/ml). Experiment data also showed that TGF-β1 can increase the expression of the mesenchymal phenotype markers (Vimentin, β-catenin), and repress the expression of the epithelial phenotype marker (E-cadherin) in HK-2 cells. At the same time, compared with the control and the TGF-β1 groups, scratching test showed that TGF-β1 promoted HK-2 cell migration. The difference was statistically significant (P 〈 0.01 ). In terms of invasion, a statistically significant difference was observed between the control group and TGF-β1 group (P 〈0. 01 ). Conclusion Taken together, our findings provide the cell model of EMT in vitro using TGF-β1.
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