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PMID: 7592825 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Dithiocarbamates induce apoptosis in thymocytes by raising the intracellular level of redox-active copper.

The Journal of biological chemistry ·Vol. 270 ·No. 44 ·1995-11-03 ·Pages 26202-8

Nobel CI, Kimland M, Lind B, Orrenius S, Slater AF

Abstract

Dithiocarbamates are metal-chelating compounds that can exert either pro-oxidant or antioxidant effects in different situations. They have recently been found to potently inhibit apoptotic cell death, an activity attributed to their antioxidant action. However, when thymocytes were exposed to pyrrolidine dithiocarbamate, an oxidation of the glutathione pool occurred within 90 min. Longer incubation resulted in cell shrinkage, chromatin fragmentation, glutathione depletion, and eventual cell lysis, which is typical of apoptosis in these cells. These changes were inhibited by inclusion of non-permeable metal chelators in the incubation medium, suggesting that pyrrolidine dithiocarbamate exerts its toxic effect by transporting a redox-active metal into the cell. This was directly confirmed when sustained 8-fold elevations of intracellular copper were detected after addition of pyrrolidine dithiocarbamate. In agreement with this, supplementation of the incubation medium with submicromolar concentrations of copper significantly potentiated pyrrolidine dithiocarbamate toxicity. We conclude that pyrrolidine dithiocarbamate exerts a powerful pro-oxidant effect on thymocytes due to its ability to transport external redox-active copper into cells. The resulting increase in glutathione disulfide may also explain the temporary anti-apoptotic activity of this compound described in other systems.

MeSH Terms
Animals Apoptosis/drug effects Cells, Cultured Chelating Agents/pharmacology Copper/analysis,metabolism,pharmacology Copper Sulfate DNA/analysis Ditiocarb/pharmacology Dose-Response Relationship, Drug Drug Synergism Glutathione/analogs & derivatives,metabolism Glutathione Disulfide Iron/analysis,metabolism Kinetics Male Oxidation-Reduction Phenanthrolines/pharmacology Pyrrolidines/pharmacology Rats Rats, Sprague-Dawley Spectrophotometry, Atomic/methods Structure-Activity Relationship Thiocarbamates/pharmacology Thymus Gland/cytology,drug effects,physiology Time Factors
Chemicals
Chelating Agents Phenanthrolines Pyrrolidines Thiocarbamates pyrrolidine dithiocarbamic acid bathocuproine sulfonate Copper DNA Ditiocarb Iron Glutathione Copper Sulfate Glutathione Disulfide
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Nobel C I
Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Kimland M
Lind B
Orrenius S
Slater A F
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1995-11-03
Pages
26202-8
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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