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作 者:李艳敏[1,2] 张昌军[2] 董毅飞[2] 邓锴[2] 彭海英[2] 刁红录[2]
机构地区:[1]武汉大学中南医院,湖北武汉430071 [2]湖北医药学院附属人民医院生殖医学中心,湖北十堰442000
出 处:《武汉大学学报(医学版)》2015年第4期524-528,共5页Medical Journal of Wuhan University
基 金:湖北省教育厅科学计划项目资助(编号:B20112103;D20142101;Q20122402)
摘 要:目的:探讨全反式视黄醛(at-Ral)对体外培养人子宫内膜异位症(EMT)在位内膜基质细胞迁移和视黄醇脱氢酶(RDH)10mRNA表达的影响。方法:体外分离培养EMT患者在位子宫内膜基质细胞(EMT-ESC)及正常人子宫内膜基质细胞(N-ESC),采用细胞划痕运动分析及real time PCR方法分别观察不同浓度at-Ral对细胞迁移及RDH10mRNA表达情况。结果:N-ESC的迁移距离及RDH10的表达随at-Ral浓度的升高而减少,1,10μmol/L组与对照组比较差异有统计学意义(P<0.05),而EMT-ESC的迁移距离及RDH10的表达随at-Ral浓度的升高而增加,1,10μmol/L组与对照组比较差异有统计学意义(P<0.05)。结论:at-Ral对内异症患者在位子宫内膜基质细胞的迁移及RDH 10mRNA表达有促进作用。Objective. To investigate the effect of all-trans-retinal(at-Ral)on the migration and retinol dehydrogenase (RDH10) mRNA expression of in vitro cultured human endometrial eutopic endo- metrial stromal cells. Methods. Endometrial stromal cells were isolated in vitro in normal women (N-ESC) and women with endometriosis (EMT-ESC). Then we observed the effects of different concentrations of at-Ral by cell scratch assay and real time PCR. Results. The migration distance and expression of RDH 10 mRNA of N-ESC decreased with the increased concentration of at-Ral. There were significant differences between 1, 10 μmol/L groups and the control group (P〈0.05), while the migration distance and expression of RDH 10 mRNA of EMT-ESC increased with the increased concentration of at-Ral. There were significant differences between 1, 10μmol/L groups and the control group (P〈0.05). Conclusion: At-Ral can promote migration and expression of RDH10 mRNA of eutopic endometrial stromal cell of endometriosis.
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