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微小RNA-93通过靶向BCL2L2抑制复发性自然流产中滋养层细胞增殖并促进细胞凋亡。

MiR-93 Inhibits Trophoblast Cell Proliferation and Promotes Cell Apoptosis by Targeting BCL2L2 in Recurrent Spontaneous Abortion.

作者信息

Liu Hai-Ning, Tang Xiu-Ming, Wang Xue-Qin, Gao Jing, Li Ni, Wang Yong-Yong, Xia Hong-Fei

机构信息

Center for Reproductive Medicine, Shandong University, Jinan, China.

Department of Reproductive Medicine, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.

出版信息

Reprod Sci. 2020 Jan;27(1):152-162. doi: 10.1007/s43032-019-00003-w. Epub 2020 Jan 1.

Abstract

Recurrent spontaneous abortion (RSA) is a common health problem that affects 1-5% of women in reproductive age. Plenty of studies have indicated that microRNAs (miRNAs) are involved in the occurrence of miscarriage. MiR-93 has a wide range of functions in mammalian tissues and plays an important role in many diseases especially for cancers. However, it remains unknown whether miR-93 is associated with human RSA. In this report, clinical samples revealed that miR-93 expression was significantly elevated in the villi tissues of RSA patients. Upregulation of miR-93 inhibited human trophoblast cells HTR-8/SVneo cell proliferation, migration, and invasiveness, but promoted cell apoptosis in vitro. Conversely, the downregulation of miR-93 reversed these effects. Bcl-2 like protein 2 (BCL2L2), a potential target gene of miR-93, was inversely correlated with miR-93 expression in the villi of clinical samples. Furthermore, the luciferase reporter system demonstrated that miR-93 directly downregulated the expression of BCL2L2 by binding a specific sequence of its 3'-untranslated region (3'UTR). Collectively, these data strongly suggest that miR-93 regulates trophoblast cell proliferation, migration, invasive, and apoptosis by targeting BCL2L2 expression and is involved in the pathogenesis of RSA.

摘要

复发性自然流产(RSA)是一个常见的健康问题,影响着1%-5%的育龄妇女。大量研究表明,微小RNA(miRNA)参与了流产的发生。MiR-93在哺乳动物组织中具有广泛的功能,在许多疾病尤其是癌症中发挥重要作用。然而,miR-93是否与人类RSA相关仍不清楚。在本报告中,临床样本显示RSA患者绒毛组织中miR-93表达显著升高。miR-93的上调抑制了人滋养层细胞HTR-8/SVneo细胞的增殖、迁移和侵袭,但在体外促进了细胞凋亡。相反,miR-93的下调逆转了这些作用。Bcl-2样蛋白2(BCL2L2)是miR-93的一个潜在靶基因,在临床样本的绒毛中与miR-93表达呈负相关。此外,荧光素酶报告系统表明,miR-93通过结合其3'-非翻译区(3'UTR)的特定序列直接下调BCL2L2的表达。总的来说,这些数据强烈表明,miR-93通过靶向BCL2L2表达来调节滋养层细胞的增殖、迁移、侵袭和凋亡,并参与RSA的发病机制。

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