Differential effects of mercury, lead, and cadmium on IL-2 production by Jurkat T cells

Mercury, lead, and cadmium are widespread and highly toxic pollutants. The aim of this study was to determine the effects of sublethal doses of CH(3)HgCl, CdCl(2), and PbCl(2) on IL-2 production by T lymphocytes. Jurkat T cells were stimulated by triggering CD3 and CD28 molecules before, in conjunct...

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Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 111(2004), 3 vom: 15. Juni, Seite 311-22
1. Verfasser: Colombo, Myrian (VerfasserIn)
Weitere Verfasser: Hamelin, Claudine, Kouassi, Edouard, Fournier, Michel, Bernier, Jacques
Format: Aufsatz
Sprache:English
Veröffentlicht: 2004
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Research Support, Non-U.S. Gov't CD28 Antigens CD3 Complex DNA-Binding Proteins Interleukin-2 Methylmercury Compounds NFATC Transcription Factors Nuclear Proteins Transcription Factors mehr... Lead 2P299V784P lead chloride 4IL61GN3YI Cadmium Chloride J6K4F9V3BA methylmercuric chloride RWZ4L3O1X0
Beschreibung
Zusammenfassung:Mercury, lead, and cadmium are widespread and highly toxic pollutants. The aim of this study was to determine the effects of sublethal doses of CH(3)HgCl, CdCl(2), and PbCl(2) on IL-2 production by T lymphocytes. Jurkat T cells were stimulated by triggering CD3 and CD28 molecules before, in conjunction with, or following heavy metal exposure. Heavy metals, individually or mixed together at equimolar concentrations, were used. Results demonstrated that low, noncytotoxic doses of metals induce tyrosine phosphorylation. Mercury and lead (1 microM) inhibit IL-2 production regardless of the state of T cell activation. Cadmium stimulated IL-2 production only in preactivated T cells. Surprisingly, a mixture of these three metals had no effect. We subsequently determined the effects of heavy metals on NFAT (nuclear factors of activated T cells) activity. When cells were stimulated by potent stimulation involving the CD3 and CD28 molecules, an increased NFAT activation was noted when the cells were exposed to mercury and to the metal mixture. Activation with PMA/calcium ionophores indicated that the target of heavy metals is located downstream from PKC and calcium mobilization. These results suggest that the state and mode of T cell activation are important parameters to consider in heavy metal toxicity
Beschreibung:Date Completed 02.08.2004
Date Revised 16.11.2017
published: Print
Citation Status MEDLINE
ISSN:1521-6616