首页|miR-34c-5p靶向poFUT1对胎盘血管形成的影响

miR-34c-5p靶向poFUT1对胎盘血管形成的影响

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目的:探讨miR-34c-5p与poFUT1 的靶向关系及对胎盘血管形成的影响.方法:利用ENCORI数据库预测miR-34c-5p与poFUT1 的结合位点,采用双荧光素酶报告实验验证.随机选取 2023 年 4 至 10 月在郑州大学第三附属医院住院的胎儿生长受限(FGR)孕妇20 例(FGR组),选择同期正常孕妇20 例为对照.采用实时荧光定量PCR法检测两组胎盘组织中miR-34c-5p和poFUT1 mRNA的表达.取脐静脉内皮细胞,分组转染miR-34c-5p模拟物及其对照(NC)、miR-34c-5p抑制物及其NC、si-poFUT1 NC、si-poFUT1、si-poFUT1+miR-34c-5p抑制物,采用CCK-8法、Transwell实验以及成管实验检测细胞转染24、48、72、96 h后的增殖能力,转染48h后的侵袭能力和成管能力.结果:FGR组和对照组胎盘组织中miR-34c-5p表达水平分别为(1.57±0.39)、(1.09±0.18),poFUT1 mRNA表达水平分别为(0.51±0.17)、(1.06±0.13),FGR组胎盘组织中miR-34c-5p表达水平高于对照组,poFUT1 mRNA表达水平低于对照组(P<0.05).与miR-34c-5p模拟物NC组比较,模拟物组侵袭细胞数和管腔节点数减少,细胞增殖活性降低(P<0.05).与miR-34c-5p抑制物NC组比较,抑制物组侵袭细胞数和管腔节点数增加,细胞增殖活性升高(P<0.05).与si-poFUT1 NC组相比,si-poFUT1 组侵袭细胞数和管腔节点数减少,细胞增殖活性降低(P<0.05),而si-poFUT1+miR-34c-5p抑制物组上述变化较si-poFUT1 组部分逆转(P<0.05).结论:miR-34c-5p可能通过调控poFUT1 影响血管内皮细胞功能,从而影响胎盘的血管形成,参与FGR的发生.
Effect of miR-34c-5p targeting poFUT1 on placental angiogenesis
Aim:To investigate the targeting relationship between miR-34c-5p and poFUT1 and the effcet on placental angiogenesis.Methods:The binding sites between miR-34c-5p and poFUT1 were predicted by ENCORI database and veri-fied by dual luciferase reporter assay.A total of 20 pregnant women with fetal growth restriction(FGR)from the Third Affili-ated Hospital of Zhengzhou University from April to October 2023 were randomly selected,with 20 normal pregnant women during the same period serving as control.The expressions of miR-34c-5p and poFUT1 mRNA in placental tissue were de-tected using quantitative PCR.Human umbilic vein endothelial cells were transfected with miR-34c-5p mimic NC,miR-34c-5p mimic,miR-34c-5p inhibitor NC,miR-34c-5p inhibitor,si-poFUT1 NC,si-poFUT1,si-poFUT1+miR-34c-5p inhibitor,respectively,and cell proliferation,invasion and tube formation were verified using the CCK-8 assay,transwell assay,and tube formation experiment.Results:The expression of miR-34c-5p was(1.57±0.39),(1.09±0.18),and that of po-FUT1 mRNA was(0.51±0.17),(1.06±0.13)in FGR and normal placental tissue;compared with control group,the ex-pression of miR-34c-5p of FGR group was higher,and that of poFUT1 mRNA was lower(P<0.05).The number of invasive cells in miR-34c-5p mimic group was less,and tube formation capacity and the cell proliferative activity were lower than those of mimic NC group(P<0.05).The number of invasive cells in miR-34c-5p inhibitor group was more,and tube forma-tion capacity and the cell proliferative activity were higher than those of inhibitor NC group(P<0.05).Compared with si-poFUT1 NC group,the number of invasive cells in si-poFUT1 group was less,and tube formation capacity and the cell prolif-erative activity were lower(P<0.05),while the changes mentioned above in si-poFUT1+miR-34c-5p inhibitor group were reversed partly(P<0.05).Conclusion:MiR-34c-5p could regulate vascular endothelial cell function by poFUT1,thereby affecting placenta angiogenesis,and involve in FGR generation.

miR-34c-5pfetal growth restrictionpoFUT1angiogenesis

刘月华、杨照远、鲁继聪、谢梦霞、郭婧、王媛媛、杨敬敬、田赟、赵明、陈冬笋、朱双慧、李珠银、丁文珺

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郑州大学第三附属医院产科 郑州 450052

miR-34c-5p 胎儿生长受限 poFUT1 血管形成

河南省医学科技攻关计划河南省医学科技攻关计划

SBGJ202002122LHGJ20190364

2024

郑州大学学报(医学版)
郑州大学

郑州大学学报(医学版)

CSTPCD北大核心
影响因子:1.246
ISSN:1671-6825
年,卷(期):2024.59(3)
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