Document Detail


Coexpression of erythropoietin and heme oxygenase genes in Hep3B cells.
MedLine Citation:
PMID:  8387947     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Exposure of Hep3B cells to metalloporphyrins (tinprotoporphyrin and heme) or cobalt chloride resulted in the production of a significant number of heme oxygenase transcripts, erythropoietin transcripts or both, as indicated by in situ hybridization. Exposure to heme 10 mumol/L resulted in a 30-fold to 40-fold increase in cells expressing erythropoietin messenger RNA (erythropoietin-positive cells) by 6 hr; this increased level remained elevated for 24 hr. Tin-protoporphyrin (10 mumol/L) produced an eightfold to 10-fold increase in erythropoietin RNA within 40 min. This value then returned to control levels by 60 min. Exposure to cobalt chloride (100 mumol/L) resulted in a 20-fold to 30-fold increase in erythropoietin expression for 5 to 20 min, returning to control by 40 min. Additionally, nuclear runoff assays demonstrated that the increase in heme oxygenase or erythropoietin messenger RNA accumulation by cobalt chloride appeared to be a result of stimulated transcription of the heme oxygenase and erythropoietin genes. However, the pattern for heme oxygenase messenger RNA induction was different from that for erythropoietin expression. Heme produced an immediate expression of heme oxygenase RNA (50-fold within 5 min) and a second sustained response during the next 24 hr. Tin-protoporphyrin also produced an immediate response (40-fold within 5 min) and remained elevated (20-fold) for 6 hr. Cobalt chloride produced a 22-fold increase within 20 min and returned to the control value by 1 hr. Thus both erythropoietin and heme oxygenase genes appear to be expressed after treatment with tin-protoporphyrin, heme or cobalt chloride; however, the time and patterns of expression are different.(ABSTRACT TRUNCATED AT 250 WORDS)
Authors:
J D Lutton; M O Griffin; M Nishimura; R D Levere; A Kappas; N G Abraham; S Shibahara
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Hepatology (Baltimore, Md.)     Volume:  17     ISSN:  0270-9139     ISO Abbreviation:  Hepatology     Publication Date:  1993 May 
Date Detail:
Created Date:  1993-06-15     Completed Date:  1993-06-15     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  8302946     Medline TA:  Hepatology     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  861-8     Citation Subset:  IM    
Affiliation:
Department of Medicine, New York Medical College, Valhalla 10595.
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MeSH Terms
Descriptor/Qualifier:
Carcinoma, Hepatocellular / genetics*
Cobalt / pharmacology
Erythropoietin / analysis,  genetics*
Gene Expression / drug effects*
Heme / pharmacology
Heme Oxygenase (Decyclizing) / genetics*
Humans
Liver Neoplasms / genetics*
Metalloporphyrins / pharmacology
Protoporphyrins / pharmacology
RNA, Messenger / analysis
Tumor Cells, Cultured
Grant Support
ID/Acronym/Agency:
AM29742/AM/NIADDK NIH HHS
Chemical
Reg. No./Substance:
0/Metalloporphyrins; 0/Protoporphyrins; 0/RNA, Messenger; 11096-26-7/Erythropoietin; 14325-05-4/tin protoporphyrin IX; 14875-96-8/Heme; 7440-48-4/Cobalt; 7646-79-9/cobaltous chloride; EC 1.14.99.3/Heme Oxygenase (Decyclizing)

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


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