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miR-93通过基质金属蛋白酶-2抑制滋养层细胞系的侵袭。

Invasion of trophoblast cell lines is inhibited by miR-93 via MMP-2.

作者信息

Pan Qiong, Niu HuiYuan, Cheng LongFei, Li XiaoQiong, Zhang QiGang, Ning Ying

机构信息

Laboratory of Clinical Genetics, Huaian Maternity and Child Health Care Hospital of Jiangsu Province, Yangzhou University, Huaian, China; Department of Gynecology and Obstetrics, Huaian Maternity and Child Health Care Hospital of Jiangsu Province, Yangzhou University, Huaian, China.

Department of Gynecology and Obstetrics, Huaian Maternity and Child Health Care Hospital of Jiangsu Province, Yangzhou University, Huaian, China.

出版信息

Placenta. 2017 May;53:48-53. doi: 10.1016/j.placenta.2017.03.008. Epub 2017 Mar 10.

Abstract

Preeclampsia (PE) is a serious pregnancy-related syndrome, which is characterized by gestational hypertension and proteinuria. The microRNA-93 (miR-93) is upregulated in the maternal plasma of patients with PE. However, the functional role of miR-93 in PE remains unknown. Here, we identified that miR-93 inhibits trophoblastic invasion, which is correlated with PE development. In immortalized trophoblast cell lines, transwell assay showed that miR-93 mimics significantly inhibited the migration and invasion of immortalized trophoblast cells, whereas miR-93 inhibitors significantly promoted cell migration and invasion. Moreover, luciferase assays confirmed that miR-93 directly bound to the 3'untranslated region of matrix metalloproteinase-2 (MMP-2), and western blotting showed that miR-93 suppressed the expression of MMP-2 at the protein levels. This study indicated that miR-93 inhibits MMP-2 and reduces migration and invasion of immortalized trophoblast cells. Thus, miR-93 may represent a potential therapeutic target for PE intervention.

摘要

子痫前期(PE)是一种严重的妊娠相关综合征,其特征为妊娠高血压和蛋白尿。微小RNA-93(miR-93)在PE患者的母体血浆中上调。然而,miR-93在PE中的功能作用尚不清楚。在此,我们发现miR-93抑制滋养层细胞侵袭,这与PE的发展相关。在永生化滋养层细胞系中,Transwell实验表明,miR-93模拟物显著抑制永生化滋养层细胞的迁移和侵袭,而miR-93抑制剂则显著促进细胞迁移和侵袭。此外,荧光素酶实验证实miR-93直接与基质金属蛋白酶-2(MMP-2)的3'非翻译区结合,蛋白质印迹法表明miR-93在蛋白质水平上抑制MMP-2的表达。本研究表明,miR-93抑制MMP-2并减少永生化滋养层细胞的迁移和侵袭。因此,miR-93可能是PE干预的潜在治疗靶点。

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