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Nitric Oxide ; 24(3): 151-9, 2011 Apr 30.
Article in English | MEDLINE | ID: mdl-21354319

ABSTRACT

No pro-apoptotic effect of dinitrosyl iron complexes (DNIC) with glutathione, cysteine or thiosulfate was established after incubation of HeLa cells in Eagle's medium. However, DNIC with thiosulfate manifested pro-apoptotic activity during incubation of HeLa cells in Versene's solution supplemented with ethylene diamine tetraacetate (EDTA) known to induce the decomposition of these DNIC. The water-soluble о-phenanthroline derivative bathophenanthroline disulfonate (BPDS) had a similar effect on DNIC with glutathione during incubation of HeLa cells in Eagle's medium. It was assumed that EDTA- or BPDS-induced pro-apoptotic effect of DNIC with thiosulfate or glutathione is coupled with the ability of decomposing DNIC to initiate S-nitrosylation of proteins localized on the surface of HeLa cells. Presumably, the pro-apoptotic effect of S-nitrosoglutathione (GS-NO) on HeLa cells preincubated in Eagle's medium is mediated by the same mechanism, although the pro-apoptotic effect based on the ability of GS-NO to initiate the release of significant amounts of NO and its oxidation to cytotoxic peroxynitrite in a reaction with superoxide should not be ruled out either. No apoptotic activity was found in the presence of bivalent iron and glutathione favoring the conversion of GS-NO into DNIC with glutathione. It is suggested that interaction of HeLa cells with intact DNIC with glutathione or thiosulfate results in the formation of DNIC bound to cell surface proteins.


Subject(s)
Apoptosis/drug effects , Iron/toxicity , Nitric Oxide Donors/toxicity , Nitric Oxide/metabolism , Nitrogen Oxides/toxicity , Sulfhydryl Compounds/toxicity , Chelating Agents/metabolism , Chelating Agents/toxicity , Cysteine/metabolism , Edetic Acid/metabolism , Edetic Acid/toxicity , Glutathione/metabolism , HeLa Cells , Humans , Iron/metabolism , Ligands , Nitric Oxide/toxicity , Nitric Oxide Donors/metabolism , Nitrogen Oxides/metabolism , Oxidants/metabolism , Oxidants/toxicity , Oxidation-Reduction , Phenanthrolines/metabolism , Phenanthrolines/toxicity , S-Nitrosoglutathione/metabolism , S-Nitrosoglutathione/toxicity , Sulfhydryl Compounds/metabolism , Thiosulfates/metabolism , Thiosulfates/toxicity
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