Long non-coding RNA NEAT1 promotes mouse granulosa cell proliferation and estradiol synthesis by sponging miR-874-3p

文献类型： 外文期刊

第一作者： Zhang, Pengju

作者： Zhang, Pengju;Wang, Weixia;Tan, Chengcheng;Liu, Xiaohui;Li, Xintao;Zhang, Lichun;Gao, Jinliang;Lin, Shan;Lin, Guangyu;Li, Xintao;Zhang, Lichun

作者机构：

关键词： long non-coding RNA; nuclear-enriched abundant transcript 1; mouse granulosa cell; apoptosis; estradiol synthesis

期刊名称：EXPERIMENTAL AND THERAPEUTIC MEDICINE （ 影响因子：2.751； 五年影响因子：2.475 ）

ISSN： 1792-0981

年卷期： 2023 年 25 卷 1 期

页码：

收录情况： SCI

摘要： It has been reported that long non-coding RNA nuclear-enriched abundant transcript 1 (NEAT1) is involved in follicular growth and multiple ovarian diseases, but not the physiological function of NEAT1 in mouse granulosa cells (mGCs). Therefore, the aim of the present study was to investigate the biological roles and regulatory mechanisms of NEAT1 in mGCs. The biological effects of NEAT1 on mGCs proliferation, apoptosis, production of 17 beta-Estradiol (E2) and progesterone (P4) were investigated using MTS, flow cytometry and enzyme-linked immunosorbent assays, respectively. The association between NEAT1 and microRNA (miR)-874-3p was verified using luciferase reporter assay and RNA immunoprecipitation analysis. The results demonstrated that the knockdown of NEAT1 in mGC cells significantly promoted mGCs cell proliferation, inhibited apoptosis and increased the production of E2 and P4 in mGCs. The interference-mediated effect of NEAT1 on mGCs could be partially reversed by the downregulation of miR-874-3p. Overall, these results indicated that NEAT1 served as a competing endogenous RNA by competitively binding with miR-874-3p, thereby modulating mGCs proliferation and the production of E2 and P4 in mGCs.

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