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MicroRNA-181a Suppresses Mouse Granulosa Cell Proliferation by Targeting Activin Receptor IIA

机译:微小RNa-181a禁止显示小鼠卵巢颗粒细胞增殖通过瞄准素受体IIa

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摘要

Activin, a member of the transforming growth factor-β superfamily, promotes the growth of preantral follicles and the proliferation of granulosa cells. However, little is known about the role of microRNAs in activin-mediated granulosa cell proliferation. Here, we reported a dose- and time-dependent suppression of microRNA-181a (miR-181a) expression by activin A in mouse granulosa cells (mGC). Overexpression of miR-181a in mGC suppressed activin receptor IIA (acvr2a) expression by binding to its 3′-untranslated region (3′-UTR), resulting in down-regulation of cyclin D2 and proliferating cell nuclear antigen expression, leading to inhibition of the cellular proliferation, while overexpression of acvr2a attenuated the suppressive effect of miR-181a on mGC proliferation. Consistent with the inhibition of acvr2a expression, miR-181a prevented the phosphorylation of the activin intracellular signal transducer, mothers against decapentaplegic homolog 2 (Smad2), leading to the inactivation of activin signaling pathway. Interestingly, we found that miR-181a expression decreased in ovaries of mice at age of 8, 12, and 21 days, as compared with that in ovaries of 3-day old mice, and its level was reduced in preantral and antral follicles of mice compared with that in primary ones. Moreover, the level of miR-181a in the blood of patients with premature ovarian failure was significantly increased compared with that in normal females. This study identifies an interplay between miR-181a and acvr2a, and reveals an important role of miR-181a in regulating granulosa cell proliferation and ovarian follicle development.
机译:激活素是转化生长因子-β超家族的成员,可促进窦前卵泡的生长和颗粒细胞的增殖。但是,关于微RNA在激活素介导的颗粒细胞增殖中的作用了解甚少。在这里,我们报道了激活素A在小鼠颗粒细胞(mGC)中对microRNA-181a(miR-181a)表达的剂量和时间依赖性抑制。 miR-181a在mGC中的过表达通过与3'-非翻译区(3'-UTR)结合而抑制了激活素受体IIA(acvr2a)的表达,从而导致细胞周期蛋白D2的下调和细胞核抗原表达的增殖,从而导致抑制细胞增殖,而acvr2a的过表达减弱了miR-181a对mGC增殖的抑制作用。与抑制acvr2a的表达一致,miR-181a阻止了激活素细胞内信号转导子的磷酸化,母亲抵抗了十足功能的同系物2(Smad2),从而导致激活素信号通路的失活。有趣的是,我们发现与3天大的小鼠卵巢相比,miR-181a在8、12和21天龄的小鼠卵巢中表达降低,并且其水平在小鼠的窦前和肛门卵泡中降低了。与小学的相比。此外,与正常女性相比,卵巢早衰患者血液中miR-181a的水平显着升高。这项研究确定了miR-181a和acvr2a之间的相互作用,并揭示了miR-181a在调节颗粒细胞增殖和卵巢卵泡发育中的重要作用。

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