Document Detail


Hydrogen sulfide-induces DNA damage and changes in apoptotic gene expression in human lung fibroblast cells.
MedLine Citation:
PMID:  17116745     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Hydrogen sulfide (H2S) has been shown previously to exert proapoptotic activity. However, the mechanism(s) by which H2S affects cell growth and function have not been addressed adequately. In this study, cultured human lung fibroblasts were treated with the H2S donor NaHS (10-75 microM; 12-48 h). NaHS caused a concentration-dependent increase in micronuclei formation (indicating DNA damage) and cell cycle arrest (G1 phase). NaHS increased expression of ku 70 and ku 80 but did not affect the expression of other DNA repair proteins such as proliferating cell nuclear antigen (PCNA) or replication protein A (rNase protection assay). NaHS treatment also resulted in stabilization of p53 coupled with induction of downstream proteins such as p21, Bax, and cytochrome c, as well as translocation of Bax from the cytosol to the mitochondria and release of cytochrome c from mitochondria. NaHS did not up-regulate cell levels of the antiapoptotic protein, Bcl-2. We propose that the genotoxic action of H2S propels the cell toward apoptotic death triggered initially by stabilization of p53 and subsequently involving a cascade of downstream products. These results are of significance as they uncover a hitherto unknown and very fundamental role for H2S in determining cell fate.
Authors:
Rajamanickam Baskar; Ling Li; Philip Keith Moore
Related Documents :
20571075 - Sensitivity of cancer cells to plk1 inhibitor gsk461364a is associated with loss of p53...
10845255 - A subset of cells expressing sv40 large t antigen contain elevated p53 levels and have ...
12151395 - Inactivation of p21waf1 sensitizes cells to apoptosis via an increase of both p14arf an...
11369765 - Activation of a p53-independent, sphingolipid-mediated cytolytic pathway in p53-negativ...
8900485 - Neuroendocrine-specific protein c (nsp-c): subcellular localization and differential ex...
14527275 - Assembly dynamics of the bacterial cell division protein ftsz: poised at the edge of st...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2006-11-20
Journal Detail:
Title:  FASEB journal : official publication of the Federation of American Societies for Experimental Biology     Volume:  21     ISSN:  1530-6860     ISO Abbreviation:  FASEB J.     Publication Date:  2007 Jan 
Date Detail:
Created Date:  2006-12-29     Completed Date:  2007-02-05     Revised Date:  2012-02-15    
Medline Journal Info:
Nlm Unique ID:  8804484     Medline TA:  FASEB J     Country:  United States    
Other Details:
Languages:  eng     Pagination:  247-55     Citation Subset:  IM    
Affiliation:
Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, 18 Medical Dr., Singapore 117597.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Apoptosis / genetics*
Cell Cycle / drug effects
Cells, Cultured
Cytochromes c / metabolism
DNA Damage*
Fibroblasts / drug effects,  metabolism
Humans
Hydrogen Sulfide / pharmacology*
Lung / cytology,  drug effects*,  metabolism
Micronucleus Tests
Multigene Family
bcl-2-Associated X Protein / metabolism
Chemical
Reg. No./Substance:
0/bcl-2-Associated X Protein; 7783-06-4/Hydrogen Sulfide; 9007-43-6/Cytochromes c

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


Previous Document:  Rapid disuse and denervation atrophy involve transcriptional changes similar to those of muscle wast...
Next Document:  Methylation of DNA polymerase beta by protein arginine methyltransferase 1 regulates its binding to ...