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

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 cadmi...

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Detalles Bibliográficos
Autores principales: Olszowski, Tomasz, Gutowska, Izabela, Baranowska-Bosiacka, Irena, Piotrowska, Katarzyna, Korbecki, Jan, Kurzawski, Mateusz, Chlubek, Dariusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424267/
https://www.ncbi.nlm.nih.gov/pubmed/25645360
http://dx.doi.org/10.1007/s12011-015-0234-6
Descripción
Sumario: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 (CdCl(2)) solutions for 48 h at final concentrations of 5 nM, 20 nM, 200 nM, and 2 μM CdCl(2). The mRNA expression and protein levels of COXs were analyzed with RT-PCR and Western blotting, respectively. Prostaglandin E(2) (PGE(2)) and stable metabolite of thromboxane B(2) (TXB(2)) 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. PGE(2) and TXB(2) production is not altered by all tested Cd concentrations; however, the significant stimulation of PGE(2) and TXB(2) 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.