Document Detail


Activation of a novel isoform of methionine adenosyl transferase 2A and increased S-adenosylmethionine turnover in lung epithelial cells exposed to hyperoxia.
MedLine Citation:
PMID:  16413417     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
S-Adenosylmethionine (SAM, AdoMet) is the most important methyl donor used for synthesis of nucleic acids, phospholipids, creatine, and polyamines and for methylation of many bioactive molecules. The metabolic response of the lung to oxidative stress of hyperoxia requires increased RNA and protein synthesis for energy metabolism, growth arrest, and antioxidant defense. We studied the production of SAM and other aspects of methionine metabolism in lung epithelial cells exposed to hyperoxia. Human lung epithelial-like (A549) and primary small airway epithelial (SAE) cells were exposed to normoxia (21% O(2)) or hyperoxia (95% O(2)). Cell methionine and S-adenosylmethionine content increased in response to hyperoxia in SAE and A549 cells. Because methionine adenosyl transferase (MAT) is the rate-limiting enzyme of the pathway, we examined the expression of a lung epithelial isoform of MAT 2A in hyperoxia. Western blots revealed a novel MAT 2A isoform expressed in both cell types, with a lower molecular mass than that described in Jurkat cells. Cloning and sequencing of the MAT 2A cDNA revealed one silent nucleotide substitution compared to that expressed in Jurkat. The lower mass of MAT 2A in both lung epithelial cells indicated that the absence of the major posttranslational modification of MAT 2A found in Jurkat. MAT 2A protein progressively increased during hyperoxic exposure in both transformed and primary lung epithelium. Increased flux of (13)C-labeled methionine to S-adenosylhomocysteine (SAH) in A549 demonstrated that SAM's methyl group was utilized, and increased formation of cystathionine indicated that at least part of SAM generated was directed toward cysteine/GSH in the transsulfuration pathway. These results indicate activation of MAT 2A and the transmethylation pathway in the metabolic response to hyperoxia in lung epithelium.
Authors:
Mihalis I Panayiotidis; Sally P Stabler; Aftab Ahmad; Aglaia Pappa; Leighton H Legros; Daniel Hernandez-Saavedra; B Kelly Schneider; Robert H Allen; Vasilis Vasiliou; Joe M McCord; Malak Kotb; Carl W White
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Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2005-11-18
Journal Detail:
Title:  Free radical biology & medicine     Volume:  40     ISSN:  0891-5849     ISO Abbreviation:  Free Radic. Biol. Med.     Publication Date:  2006 Jan 
Date Detail:
Created Date:  2006-01-17     Completed Date:  2006-04-13     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  8709159     Medline TA:  Free Radic Biol Med     Country:  United States    
Other Details:
Languages:  eng     Pagination:  348-58     Citation Subset:  IM    
Affiliation:
Department of Pediatrics, National Jewish Medical and Research Center, 1400 Jackson Street, Denver, CO 80206, USA.
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MeSH Terms
Descriptor/Qualifier:
Cell Line, Tumor
Enzyme Activation / physiology
Epithelial Cells / metabolism*
Humans
Hyperoxia / metabolism*
Isoenzymes / metabolism
Lung / metabolism*
Methionine Adenosyltransferase / metabolism*
Oxidative Stress / physiology
S-Adenosylmethionine / metabolism*
Time Factors
Tumor Cells, Cultured
Grant Support
ID/Acronym/Agency:
AA 11885/AA/NIAAA NIH HHS; AG 09834/AG/NIA NIH HHS; HL 52732/HL/NHLBI NIH HHS; HL 56263/HL/NHLBI NIH HHS; HL 57144/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
0/Isoenzymes; 29908-03-0/S-Adenosylmethionine; EC 2.5.1.6/Methionine Adenosyltransferase

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


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