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牛体内促炎细胞因子肿瘤坏死因子-α(TNFα)、白细胞介素6(IL6)及其受体的卵泡表达:TNFα、IL6和巨噬细胞抑制卵泡膜雄激素生成 。

Follicular expression of pro-inflammatory cytokines tumour necrosis factor-α (TNFα), interleukin 6 (IL6) and their receptors in cattle: TNFα, IL6 and macrophages suppress thecal androgen production .

作者信息

Samir Moafaq, Glister Claire, Mattar Dareen, Laird Mhairi, Knight Phil G

机构信息

School of Biological SciencesUniversity of Reading, Whiteknights, Reading, UK.

School of Biological SciencesUniversity of Reading, Whiteknights, Reading, UK

出版信息

Reproduction. 2017 Jul;154(1):35-49. doi: 10.1530/REP-17-0053. Epub 2017 Apr 21.

Abstract

Pro-inflammatory cytokines secreted by macrophages and other cell types are implicated as intraovarian factors affecting different aspects of ovarian function including follicle and corpus luteum 'turnover', steroidogenesis and angiogenesis. Here, we compared granulosal (GC) and thecal (TC) expression of TNF, IL6 and their receptors (TNFRSF1A, TNFRSF1B and IL6R) during bovine antral follicle development; all five mRNA transcripts were detected in both GC and TC and statistically significant cell-type and follicle stage-related differences were evident. Since few studies have examined cytokine actions on TC steroidogenesis, we cultured TC under conditions that retain a non-luteinized 'follicular' phenotype and treated them with TNFα and IL6 under basal and LH-stimulated conditions. Both TNFα and IL6 suppressed androgen secretion concomitantly with CYP17A1 and LHCGR mRNA expression. In addition, TNFα reduced INSL3, HSD3B1 and NOS3 expression but increased NOS2 expression. IL6 also reduced LHCGR and STAR expression but did not affect HSD3B1, INSL3, NOS2 or NOS3 expression. As macrophages are a prominent source of these cytokines , we next co-cultured TC with macrophages and observed an abolition of LH-induced androgen production accompanied by a reduction in CYP17A1, INSL3, LHCGR, STAR, CYP11A1 and HSD3B1 expression. Exposure of TC to bacterial lipopolysaccharide also blocked LH-induced androgen secretion, an effect reduced by a toll-like receptor blocker (TAK242). Collectively, the results support an inhibitory action of macrophages on thecal androgen production, likely mediated by their secretion of pro-inflammatory cytokines that downregulate the expression of LHCGR, CYP17A1 and INSL3. Bovine theca interna cells can also detect and respond directly to lipopolysaccharide.

摘要

巨噬细胞和其他细胞类型分泌的促炎细胞因子被认为是影响卵巢功能不同方面的卵巢内因子,包括卵泡和黄体的“更替”、类固醇生成和血管生成。在此,我们比较了牛窦卵泡发育过程中颗粒细胞(GC)和卵泡膜细胞(TC)中肿瘤坏死因子(TNF)、白细胞介素6(IL6)及其受体(TNFRSF1A、TNFRSF1B和IL6R)的表达;在GC和TC中均检测到所有五种mRNA转录本,并且细胞类型和卵泡阶段相关的差异具有统计学意义。由于很少有研究探讨细胞因子对TC类固醇生成的作用,我们在保留非黄体化“卵泡”表型的条件下培养TC,并在基础和促黄体生成素(LH)刺激条件下用TNFα和IL6处理它们。TNFα和IL6均抑制雄激素分泌,同时伴有细胞色素P450 17α-羟化酶(CYP17A1)和促黄体生成素/绒毛膜促性腺激素受体(LHCGR)mRNA表达降低。此外,TNFα降低胰岛素样肽3(INSL3)、3β-羟基类固醇脱氢酶1型(HSD3B1)和一氧化氮合酶3(NOS3)的表达,但增加一氧化氮合酶2(NOS2)的表达。IL6也降低LHCGR和类固醇生成急性调节蛋白(STAR)的表达,但不影响HSD3B1、INSL3、NOS2或NOS3的表达。由于巨噬细胞是这些细胞因子的主要来源,接下来我们将TC与巨噬细胞共培养,观察到LH诱导的雄激素产生被消除,同时CYP17A1、INSL3、LHCGR、STAR、细胞色素P450 11A1(CYP11A1)和HSD3B1的表达降低。将TC暴露于细菌脂多糖也会阻断LH诱导的雄激素分泌,这种作用可被一种Toll样受体阻滞剂(TAK242)减弱。总体而言,这些结果支持巨噬细胞对卵泡膜雄激素产生具有抑制作用,这可能是由它们分泌的促炎细胞因子介导的,这些细胞因子下调LHCGR、CYP

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