Document Detail


Organotin-induced caspase activation and apoptosis in human peripheral blood lymphocytes.
MedLine Citation:
PMID:  11453724     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
In the present study, we show that the immunotoxicant, tributyltin (TBT), induces a dose-dependent activation of caspases followed by typical apoptotic morphology in resting human peripheral blood lymphocytes. TBT also caused an early loss of mitochondrial membrane potential (Delta(Psi)(m)) and release of cytochrome c, suggesting that apoptosis was triggered by the mitochondrial pathway. When CD4+ T-cells were sorted from peripheral blood and exposed to TBT for 30 min, caspase activation and apoptosis were induced. Interestingly, in the sorted CD8+ T-cell population, caspase activation was not observed until 2 h of TBT exposure, suggesting that these cells were more resistant toward TBT. Moreover, a time-dependent induction of caspase activity was also detected in CD3-stimulated peripheral blood lymphocytes. This caspase activation was not associated with cytochrome c release or loss of mitochondrial Delta(Psi) and did not lead to apoptotic morphology, although it did lead to both PARP and DFF cleavage. We also noticed a concomitant induction of Hsp27, and it awaits to be seen if this chaperone may interfere with the processing of nuclear protein substrates downstream from these primary caspase-3 substrates. Moreover, no increase in caspase activation or induction of apoptosis was observed after TBT treatment in these cells. Instead, the cells were directed toward necrotic deletion. Taken together, these data suggest that TBT-induced deletion of peripheral lymphocytes is likely to be a component in the overall risk for immunotoxic responses in exposed humans.
Authors:
H Stridh; I Cotgreave; M Müller; S Orrenius; D Gigliotti
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Chemical research in toxicology     Volume:  14     ISSN:  0893-228X     ISO Abbreviation:  Chem. Res. Toxicol.     Publication Date:  2001 Jul 
Date Detail:
Created Date:  2001-07-16     Completed Date:  2001-12-04     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  8807448     Medline TA:  Chem Res Toxicol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  791-8     Citation Subset:  IM    
Affiliation:
Institute of Environmental Medicine, Department of Medicine, Division of Respiratory Medicine, Karolinska Institutet, Stockholm, Sweden. helene.stridh@ks.se
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MeSH Terms
Descriptor/Qualifier:
Antigens, CD3 / blood,  immunology,  metabolism
Apoptosis / drug effects*
CD4-Positive T-Lymphocytes / drug effects
CD8-Positive T-Lymphocytes / drug effects
Caspases / metabolism*
Cytochrome c Group / drug effects
Dose-Response Relationship, Drug
Enzyme Activation
Humans
Kinetics
Lymphocytes / blood,  drug effects*,  enzymology
Membrane Potentials
Mitochondria / drug effects
Organotin Compounds / pharmacology*
Trialkyltin Compounds / pharmacology*
Chemical
Reg. No./Substance:
0/Antigens, CD3; 0/Cytochrome c Group; 0/Organotin Compounds; 0/Trialkyltin Compounds; 688-73-3/tributyltin; EC 3.4.22.-/Caspases

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


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