Department of Gynecology, Obstetrics and Gynecology Hospital of Fudan University, No. 128, Shenyang Road, Shanghai, 200090, China.
Department of Obstetrics, Obstetrics and Gynecology Hospital of Fudan University, No. 128, Shenyang Road, Shanghai, 200090, China.
Sci Rep. 2018 Jun 12;8(1):8944. doi: 10.1038/s41598-018-27296-2.
We investigated whether stable eukaryotic translation initiation factor 3e/inter 6 (eIF-3e/Int6) RNA-silencing (siRNA-Int6) can ameliorate pre-eclampsia (PE) by promoting angiogenesis in an N-nitro-L-arginine methyl ester (L-NAME)-induced rat pre-eclampsia (PE) model. Twenty-four pregnant female Sprague-Dawley rats were allocated into 4 groups, including controls (Con) without any treatment, and 18 from gestational day (GD) 7 to GD17 L-NAME-treated rats, which were divided into stable siRNA-Int6 transfected (siRNA-Int6), negative vector control siRNA (NC-siRNA) and PE control (PE-Con) groups. All adenovirus siRNA transfections were performed on GD7 via intravenous tail injection. On GD0, GD11 and GD17, blood pressure, and on GD6 and GD17, protein estimations in 24 h urine samples were conducted. All animals were sacrificed on GD18. In the PE-Con group, placental Int6 was expressed to a significantly greater level than in the Con group, which was reversed by the application of siRNA-Int6. Blood pressure and proteinuria were significantly lower in the siRNA-Int6 group than in the PRE-Con group. As shown by CD31 and IB4 expression, placental micro-vascular density (MVD) was significantly higher in the siRNA-Int6 group than in the PE-Con and NC-siRNA groups, which has accompanied by enhanced trophoblast invasion. Int6 silencing alleviated the maternal clinical manifestations of pre-eclampsia and promoted placental angiogenesis in pregnant L-NAME-treated rats.
我们研究了稳定的真核翻译起始因子 3e/Inter 6(eIF-3e/Int6)RNA 沉默(siRNA-Int6)是否可以通过促进血管生成来改善 N-硝基-L-精氨酸甲酯(L-NAME)诱导的大鼠子痫前期(PE)模型中的子痫前期(PE)。24 只妊娠雌性 Sprague-Dawley 大鼠被分配到 4 组,包括未接受任何治疗的对照组(Con)和从妊娠第 7 天到第 17 天接受 L-NAME 治疗的大鼠 18 只,它们分为稳定的 siRNA-Int6 转染(siRNA-Int6)、阴性载体对照 siRNA(NC-siRNA)和 PE 对照组(PE-Con)。所有腺病毒 siRNA 转染均在 GD7 通过静脉尾注射进行。在 GD0、GD11 和 GD17 进行血压检测,在 GD6 和 GD17 进行 24 小时尿蛋白测定。所有动物均在 GD18 处死。在 PE-Con 组中,胎盘 Int6 的表达水平明显高于 Con 组,而 siRNA-Int6 的应用则逆转了这一情况。与 PE-Con 组相比,siRNA-Int6 组的血压和蛋白尿显著降低。如 CD31 和 IB4 表达所示,siRNA-Int6 组胎盘微血管密度(MVD)明显高于 PE-Con 和 NC-siRNA 组,同时滋养细胞侵袭增强。Int6 沉默缓解了子痫前期的母体临床表现,并促进了孕 L-NAME 处理大鼠的胎盘血管生成。