Department of Gynaecology, Shanghai Dahua Hospital, Shanghai, PR. China.
Bioengineered. 2022 May;13(5):12289-12297. doi: 10.1080/21655979.2022.2070965.
MicroRNA-613 (miR-613) inhibits granulosa cell proliferation, suggesting its involvement in polycystic ovary syndrome (PCOS). We predicted that long non-coding RNA (lncRNA) HLA-F antisense RNA 1 (HLA-F-AS1) could interact with premature miR-613. We then explored the crosstalk between HLA-F-AS1 and miR-613 in PCOS. In this study, follicular fluid donated by 58 healthy controls and 58 PCOS patients was used to analyze the expression of HLA-F-AS1 and miR-613 (mature and premature). The direct interaction between HLA-F-AS1 and premature miR-613 was evaluated by RNA pull-down assay. Overexpression of both HLA-F-AS1 and miR-613 was achieved in granulosa cells to assess their interactions. Cell proliferation and apoptosis were detected with BrdU assay and cell apoptosis assay, respectively. We found that miR-613 was highly expressed in PCOS, while HLA-F-AS1 was downregulated in PCOS. HLA-F-AS1 directly interacted with premature miR-613, and overexpression of HLA-F-AS1 increased the expression levels of premature miR-613, but decreased the expression levels of mature miR-613. HLA-F-AS1 increased ovarian granulosa cell proliferation and inhibited cell apoptosis. MiR-613 played an opposite role and suppressed the role of HLA-F-AS1. Therefore, HLA-F-AS1 may inhibit the maturation of miR-613 in PCOS to promote ovarian granulosa cell proliferation and inhibit cell apoptosis.
miR-613(miR-613)抑制颗粒细胞增殖,提示其参与多囊卵巢综合征(PCOS)。我们预测长链非编码 RNA(lncRNA)HLA-F 反义 RNA 1(HLA-F-AS1)可能与过早的 miR-613 相互作用。然后,我们研究了 HLA-F-AS1 和 miR-613 在 PCOS 中的相互作用。在这项研究中,使用了 58 名健康对照者和 58 名 PCOS 患者的卵泡液来分析 HLA-F-AS1 和 miR-613(成熟和早期)的表达。通过 RNA 下拉测定评估 HLA-F-AS1 和早期 miR-613 之间的直接相互作用。在颗粒细胞中过表达 HLA-F-AS1 和 miR-613 以评估它们的相互作用。用 BrdU 测定和细胞凋亡测定分别检测细胞增殖和细胞凋亡。我们发现 miR-613 在 PCOS 中高度表达,而 HLA-F-AS1 在 PCOS 中下调。HLA-F-AS1 与早期 miR-613 直接相互作用,过表达 HLA-F-AS1 增加了早期 miR-613 的表达水平,但降低了成熟 miR-613 的表达水平。HLA-F-AS1 增加卵巢颗粒细胞增殖并抑制细胞凋亡。miR-613 则起到相反的作用,抑制了 HLA-F-AS1 的作用。因此,HLA-F-AS1 可能通过抑制 miR-613 的成熟来促进卵巢颗粒细胞增殖并抑制细胞凋亡。