Document Detail


Alterations in cytoskeletal protein sulfhydryls and cellular glutathione in cultured cells exposed to cadmium and nickel ions.
MedLine Citation:
PMID:  8442019     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
To understand the mechanisms of Cd2+ and Ni2+ cytotoxicity, we have studied the effects of these two metal ions on the organization of cytoskeletal elements, microtubules (MT) and microfilaments (MF), cytoskeletal protein sulfhydryls and cellular glutathione (GSH) in cultured 3T3 cells. At a metal ion dose that caused 95% inhibition of DNA synthesis, Cd2+ (10 microM, 16 h exposure) induced MT depolymerization whereas Ni2+ (2 mM, 20 h exposure) elicited MT aggregation and bundling. Under these conditions, Cd2+ and Ni2+ also caused MF aggregation and redistribution. Furthermore, exposure of cells to Cd2+ resulted in a dose-dependent increase in cytoskeletal protein sulfhydryls and cellular GSH levels. In contrast, treatment of cells with Ni2+ resulted in a dose-dependent decrease in cytoskeletal protein sulfhydryls as well as cellular GSH content. Time course studies showed that cells exposed to 10 microM Cd2+ exhibited a biphasic response in regulating their cytoskeletal protein sulfhydryls and cellular GSH, e.g. an initial decrease followed by a steady recovery and overshooting upon prolonged incubation. However, restoration of cytoskeletal protein sulfhydryls occurred approximately 2 h after commencement of cellular GSH recovery in Cd(2+)-treated cells. These results suggest that cellular GSH may play an important role in regulating cytoskeletal protein sulfhydryls. On the other hand, decrease of cellular GSH induced by Ni2+ might facilitate oxidation of cytoskeletal protein sulfhydryls and formation of disulfide bonds between individual MT polymers which would favor MT aggregation in Ni(2+)-exposed cells. In addition, we also demonstrated that elevation of cellular GSH in Cd(2+)-treated cells probably resulted from new GSH synthesis.
Authors:
W Li; Y Zhao; I N Chou
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Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Toxicology     Volume:  77     ISSN:  0300-483X     ISO Abbreviation:  Toxicology     Publication Date:  1993 Jan 
Date Detail:
Created Date:  1993-03-30     Completed Date:  1993-03-30     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  0361055     Medline TA:  Toxicology     Country:  NETHERLANDS    
Other Details:
Languages:  eng     Pagination:  65-79     Citation Subset:  IM    
Affiliation:
Department of Microbiology, Boston University School of Medicine, MA 02118.
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MeSH Terms
Descriptor/Qualifier:
3T3 Cells
Animals
Cadmium / toxicity*
DNA / biosynthesis,  drug effects
Dose-Response Relationship, Drug
Glutathione / analysis,  drug effects*
Mice
Microfilaments / drug effects*
Microscopy, Fluorescence
Microtubules / drug effects*
Nickel / toxicity*
Sulfhydryl Compounds / analysis*
Tritium
Grant Support
ID/Acronym/Agency:
R01-ES 03543/ES/NIEHS NIH HHS
Chemical
Reg. No./Substance:
0/Sulfhydryl Compounds; 10028-17-8/Tritium; 70-18-8/Glutathione; 7440-02-0/Nickel; 7440-43-9/Cadmium; 9007-49-2/DNA

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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