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作 者:杨洋[1] 张少华[1] 李亚军[1] 韩彬[1] 马媛[2] YANG Yang ZHANG Shaohua LI Yajun HAN Bin MA Yuan(First Affiliated Hospital,Xi'an Medical University,Reproductive Medicine Center,Tangdu Hospital,Fourth Military Medical Universit)
机构地区:[1]西安医学院第一附属医院,陕西西安710077 [2]第四军医大学唐都医院生殖医学中心,陕西西安710038
出 处:《细胞与分子免疫学杂志》2017年第8期1102-1107,共6页Chinese Journal of Cellular and Molecular Immunology
基 金:陕西省科技计划项目(S2016YFSF0367)
摘 要:目的研究子痫前期相关微小RNA-18a(miR-18a)对人正常滋养细胞(HTR8)中雌激素受体1(ER1)的调控作用及对HTR8细胞周期及凋亡的影响。方法使用miR-18a前体分子(pre-miR-18a)分组转染HTR8细胞,实验分为pre-miRNA阴性对照组、miR-18a过表达组、miR-18a抑制组。反转录PCR(RT-PCR)检测转染后各组细胞中miR-18a mRNA的表达水平;RT-PCR及Western blot法分别检测各组细胞中miR-18a的靶基因ER1在mRNA和蛋白水平的表达;流式细胞术检测转染后各组细胞周期及凋亡的变化。结果与pre-miRNA阴性对照组相比,miR-18a过表达和miR-18a抑制均获得明显效果;抑制miR-18a表达后,ER1 mRNA和蛋白水平增加;过表达和抑制miR-18a对HTR8细胞周期无明显影响;抑制miR-18a可增加HTR8细胞凋亡。结论抑制miR-18a的水平增加HTR8人正常滋养细胞雌激素受体1的表达并促进细胞凋亡。Objective To investigate the role of pre-eclampsia related miR-18 a in regulating estrogen receptor 1( ER1)expression,cell cycle and apoptosis in HTR8 human trophoblasts. Methods HTR8 cells were transfected with synthesized negative control( NC) miRNA,miR-18 a and miR-18 a inhibitor,respectively. The mRNA expressions of miR-18 a and ER1 were determined by reverse transcription PCR( RT-PCR). The protein expression level of ER1 was examined by Western blotting. The cell cycle and apoptosis were evaluated by flow cytometry. Results The mRNA level of miR-18 a was significantly up-regulated in miR-18a-transfected group,while down-regulated in miR-18 a inhibitor group as compared with the NC group in HTR8 cells. Compared with the NC group,both mRNA and protein expression levels of ER1 were significantly higher in the miR-18 a inhibitor group. Cell cycle analysis showed that no significant difference was observed among the three groups. The apoptosis rate was significantly higher in the miR-18 a inhibitor group as compared with the other two groups.Conclusion Inhibition of miR-18 a increases the expression of ER1 and promotes apoptosis in HTR8 human trophoblasts.
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