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肿瘤坏死因子-α在小鼠颗粒细胞中诱导血清淀粉样蛋白A3的产生。

Tumor necrosis factor-alpha induces serum amyloid A3 in mouse granulosa cells.

作者信息

Son Deok-Soo, Roby Katherine F, Terranova Paul F

机构信息

Center for Reproductive Sciences and Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, Kansas 66160, USA.

出版信息

Endocrinology. 2004 May;145(5):2245-52. doi: 10.1210/en.2003-1261. Epub 2004 Jan 28.

Abstract

TNF-alpha has significant inhibitory effects on steroidogenesis and folliculogenesis and is associated with several inflammatory responses. Because ovulation is an inflammatory reaction, the effects of TNF on the family of acute-phase proteins in granulosa cells were investigated. Granulosa cells from immature mice at 28 d of age were cultured in the presence of 10 ng TNF/ml for 24 h. Serum amyloid A3 (SAA3), a main acute-phase protein, was induced by TNF in granulosa cells. The other isoforms of serum amyloid proteins SAA1, SAA2, and SAA4 were neither expressed in granulosa cells nor induced by TNF. TNF did not induce SAA3 mRNA in granulosa cells from TNF receptor type 1 (TNFR1) knockout mice, although SAA3 mRNA was induced within 3 h after TNF treatment in wild-type cells. Two SAA3 promoters, -617/+73 and -198/+73, were responsive to TNF and to p65, a component of the TNF signaling molecule nuclear factor (NF)-kappaB. The -106/+73 promoter of SAA3 lacking a NF-kappaB-like site was not responsive to TNF or p65. In granulosa cells from TNFR1 knockout mice, the SAA3 promoter (-198/+73) was responsive to transfection with the p65 component of NF-kappaB, but neither TNF treatment nor overexpression of the p50 component of NF-kappaB increased promoter activity. Similar results were observed in the murine ovarian granulosa tumor cell line (OV3121-1). Overexpression of the inhibitor of NF-kappaB (called IkappaB) blocked SAA3 promoter activity induced by TNF and by p65 in OV3121-1 cells. Closer analysis of deletion mutants of the SAA3 promoter revealed the necessity of a NF-kappaB like site for responsiveness to TNF in the OV3121-1 cells. TNF rapidly increased p65 in OV3121-1 nuclei when compared with controls not treated with TNF. TNF also increased phospho-IkB and SAA3 in whole-cell homogenates as determined by Western blots. Thus, TNF likely increased SAA3 promoter activity and protein by activating NF-kappaB signaling via TNFR1 in mouse granulosa cells. SAA3 is a novel gene in granulosa cells with yet unknown functions in the ovary.

摘要

肿瘤坏死因子-α(TNF-α)对类固醇生成和卵泡生成具有显著抑制作用,并与多种炎症反应相关。由于排卵是一种炎症反应,因此研究了TNF对颗粒细胞中急性期蛋白家族的影响。将28日龄未成熟小鼠的颗粒细胞在含有10 ng/ml TNF的条件下培养24小时。主要急性期蛋白血清淀粉样蛋白A3(SAA3)在颗粒细胞中被TNF诱导产生。血清淀粉样蛋白的其他亚型SAA1、SAA2和SAA4在颗粒细胞中既不表达,也不被TNF诱导。TNF在肿瘤坏死因子受体1(TNFR1)基因敲除小鼠的颗粒细胞中未诱导SAA3 mRNA表达,尽管在野生型细胞中TNF处理后3小时内SAA3 mRNA就被诱导表达。两个SAA。3启动子,-617/+73和-198/+73,对TNF和TNF信号分子核因子(NF)-κB的一个组分p65有反应。缺乏NF-κB样位点的SAA3的-106/+73启动子对TNF或p65无反应。在TNFR1基因敲除小鼠的颗粒细胞中,SAA3启动子(-198/+73)对用NF-κB的p65组分进行转染有反应,但TNF处理或NF-κB的p50组分的过表达均未增加启动子活性。在小鼠卵巢颗粒细胞瘤细胞系(OV3121-1)中也观察到类似结果。NF-κB抑制剂(称为IkappaB)的过表达阻断了TNF和p65在OV3121-1细胞中诱导的SAA3启动子活性。对SAA3启动子缺失突变体的进一步分析揭示了在OV3121-1细胞中对TNF反应需要一个NF-κB样位点。与未用TNF处理的对照相比,TNF使OV3121-1细胞核中的p65迅速增加。通过蛋白质印迹法测定,TNF还增加了全细胞匀浆中的磷酸化IkappaB和SAA3。因此,TNF可能通过在小鼠颗粒细胞中经由TNFR1激活NF-κB信号通路来增加SAA3启动子活性和蛋白质表达。SAA3是颗粒细胞中的一个新基因,在卵巢中的功能尚不清楚。

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