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镉对THP-1巨噬细胞中COX-1和COX-2基因、蛋白质表达及酶活性的影响

The Effect of Cadmium on COX-1 and COX-2 Gene, Protein Expression, and Enzymatic Activity in THP-1 Macrophages.

作者信息

Olszowski Tomasz, Gutowska Izabela, Baranowska-Bosiacka Irena, Piotrowska Katarzyna, Korbecki Jan, Kurzawski Mateusz, Chlubek Dariusz

机构信息

Department of Hygiene and Epidemiology, Pomeranian Medical University, Powstańców Wlkp. 72 Av, 70-111, Szczecin, Poland.

出版信息

Biol Trace Elem Res. 2015 Jun;165(2):135-44. doi: 10.1007/s12011-015-0234-6. Epub 2015 Feb 3.

Abstract

The aim of this study was to examine the effects of cadmium in concentrations relevant to those detected in human serum on cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) expression at mRNA, protein, and enzyme activity levels in THP-1 macrophages. Macrophages were incubated with various cadmium chloride (CdCl2) solutions for 48 h at final concentrations of 5 nM, 20 nM, 200 nM, and 2 μM CdCl2. The mRNA expression and protein levels of COXs were analyzed with RT-PCR and Western blotting, respectively. Prostaglandin E2 (PGE2) and stable metabolite of thromboxane B2 (TXB2) concentrations in culture media were determined using ELISA method. Our study demonstrates that cadmium at the highest tested concentrations modulates COX-1 and COX-2 at mRNA level in THP-1 macrophages; however, the lower tested cadmium concentrations appear to inhibit COX-1 protein expression. PGE2 and TXB2 production is not altered by all tested Cd concentrations; however, the significant stimulation of PGE2 and TXB2 production is observed when macrophages are exposed to both cadmium and COX-2 selective inhibitor, NS-398. The stimulatory effect of cadmium on COXs at mRNA level is not reflected at protein and enzymatic activity levels, suggesting the existence of some posttranscriptional, translational, and posttranslational events that result in silencing of those genes' expression.

摘要

本研究的目的是检测与人体血清中检测到的浓度相关的镉,对THP-1巨噬细胞中环氧合酶-1(COX-1)和环氧合酶-2(COX-2)在mRNA、蛋白质和酶活性水平上表达的影响。巨噬细胞与不同浓度的氯化镉(CdCl2)溶液孵育48小时,最终浓度分别为5 nM、20 nM、200 nM和2 μM CdCl2。分别用RT-PCR和蛋白质印迹法分析COXs的mRNA表达和蛋白质水平。采用ELISA法测定培养基中前列腺素E2(PGE2)和血栓素B2(TXB2)稳定代谢产物的浓度。我们的研究表明,在最高测试浓度下,镉可调节THP-1巨噬细胞中COX-1和COX-2的mRNA水平;然而,较低测试浓度的镉似乎会抑制COX-1蛋白的表达。所有测试的镉浓度均未改变PGE2和TXB2的产生;然而,当巨噬细胞同时暴露于镉和COX-2选择性抑制剂NS-398时,观察到PGE2和TXB2产生受到显著刺激。镉在mRNA水平上对COXs的刺激作用在蛋白质和酶活性水平上未得到体现,这表明存在一些转录后、翻译和翻译后事件导致这些基因的表达沉默。

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