Suppr超能文献

颗粒细胞和膜细胞中 microRNA 221 的表达:激素调节与功能。

MicroRNA 221 expression in theca and granulosa cells: hormonal regulation and function.

机构信息

Department of Animal Science, Oklahoma State University, Stillwater, OK.

出版信息

J Anim Sci. 2018 Mar 6;96(2):641-652. doi: 10.1093/jas/skx069.

Abstract

Small noncoding RNA molecules (miRNA) regulate protein levels in a post-transcriptional manner by partial base pairing to the 3'-UTR of target genes thus mediating degradation or translational repression. Previous studies indicate that numerous miRNA regulate the biosynthesis of intraovarian hormones, and emerging evidence indicates that one of these, miRNA-221 (MIR221), may be a modulator of ovarian function. However, the hormonal control of ovarian MIR221 is not known. The objectives of this study were to investigate the developmental and hormonal regulation of MIR221 expression in granulosa (GC) and theca cell (TC) and its possible role in regulating follicular function. Bovine ovaries were collected from a local abattoir and GC and TC were obtained from small (<6 mm) and large (≥8 mm) follicles. In Exp. 1, GCs of small follicles had 9.7-fold greater (P < 0.001) levels of MIR221 than those of large follicles, and TCs of large follicles had 3.7-fold greater (P < 0.001) levels of MIR221 than those of small follicles. In large follicles, abundance of MIR221 was 66.6-fold greater (P < 0.001) in TCs than in GCs. In small follicles, MIR221 abundance did not differ (P = 0.14) between GC and TCs. In vitro Exp. 2, 3, and 4 revealed that treatment of bovine TCs with various steroids, phytoestrogens, IGF1, forskolin, and dibutyryl cyclic adenosine monophosphate had no effect (P > 0.35) on MIR221 expression, whereas treatment with fibroblast growth factor 9 (FGF9) and FGF2 increased (P < 0.001) TC MIR221 abundance 1.7- to 2.5-fold. In Exp. 5, FGF9 increased (P < 0.05) GC MIR221 abundance by 1.7- and 2.0-fold in small and large follicles, respectively. The role of MIR221 in GC steroidogenesis was investigated in Exp. 6 and it was found that transfection with a MIR221 mimic reduced (P < 0.01) GC estradiol and progesterone production induced by FSH and IGF1, whereas transfection with MIR221 inhibitor had little or no effect. We conclude that thecal MIR221 expression is increased by FGF9 and increased MIR221 may act to inhibit GC steroidogenesis in cattle.

摘要

小的非编码 RNA 分子(miRNA)通过与靶基因 3'-UTR 的部分碱基配对以转录后方式调节蛋白质水平,从而介导降解或翻译抑制。先前的研究表明,许多 miRNA 调节卵巢内激素的生物合成,并且新出现的证据表明,其中之一,miRNA-221(MIR221),可能是卵巢功能的调节剂。然而,卵巢 MIR221 的激素调控尚不清楚。本研究的目的是研究颗粒细胞(GC)和膜细胞(TC)中 MIR221 表达的发育和激素调节及其在调节卵泡功能中的可能作用。从小牛屠宰场收集牛卵巢,并从小(<6mm)和大(≥8mm)卵泡中获得 GC 和 TC。在实验 1 中,小卵泡的 GC 中 MIR221 的水平比大卵泡高 9.7 倍(P<0.001),大卵泡的 TC 中 MIR221 的水平比小卵泡高 3.7 倍(P<0.001)。在大卵泡中,TC 中 MIR221 的丰度比 GC 高 66.6 倍(P<0.001)。在小卵泡中,GC 和 TC 之间的 MIR221 丰度没有差异(P=0.14)。体外实验 2、3 和 4 表明,用各种类固醇、植物雌激素、IGF1、毛喉素和二丁酰环腺苷单磷酸处理牛 TC 对 MIR221 表达没有影响(P>0.35),而用成纤维细胞生长因子 9(FGF9)和 FGF2 处理则分别增加了 TC MIR221 丰度 1.7-2.5 倍。在实验 5 中,FGF9 分别增加了小和大卵泡中 GC MIR221 的丰度 1.7-2.0 倍。在实验 6 中研究了 MIR221 在 GC 甾体生成中的作用,发现转染 MIR221 模拟物减少了 FSH 和 IGF1 诱导的 GC 雌二醇和孕酮的产生(P<0.01),而转染 MIR221 抑制剂几乎没有或没有影响。我们得出结论,MIR221 的表达在牛的卵泡中增加,增加的 MIR221 可能抑制 GC 甾体生成。

相似文献

引用本文的文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验