Document Detail


Proliferation-associated differences in the spatial and temporal expression of gap junction genes in rat liver.
MedLine Citation:
PMID:  7601414     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
After a 70% partial hepatectomy (PH), the steady-state levels of Connexin (Cx)32, Cx26, and Cx43 messenger RNA (mRNA) transcripts each displayed unique patterns of temporal expression. Within 1 hour after surgical resection, increased expression of all three Cx mRNAs was observed. Subsequently, the level of Cx32 mRNA transcripts transiently decreased to a nadir at 12 hours. Comparisons of the spatial changes with previously reported hepatocyte proliferation kinetics induced by PH demonstrated that hepatocytes before S-phase "remodel" their GJs. Within 1 to 5 hours post-PH, midzonal hepatocytes exhibited diffuse membrane staining different from the normal punctate distribution. Subsequently, midzonal hepatocytes expressed colocalized punctate Cx32 and Cx26 immunostaining. Because the changes occurred in midzonal hepatocytes before 24 hours post-PH, near the peak of hepatocyte DNA synthesis, these findings indicate that Cx26 is enhanced in hepatocytes before the onset of S-phase. In contrast to the restricted expression of Cx43 in Glisson's capsule in adult liver, Cx43 protein and mRNA were enhanced specifically in proliferating bile duct and perisinusoidal cells post-PH. PH performed during continuous administration of 2-acetylaminofluorene (AAF) prevented changes in Cx32 and Cx26 staining observed in the absence of AAF. Proliferating oval cells were found to express diffuse Cx43 immunoreactivity. On day 11 post-PH and AAF, basophilic hepatocytes displayed both punctate Cx32 and Cx26 staining, whereas bile ducts and perisinusoidal cells expressed Cx43. These findings indicate that alterations in Cx32 and Cx26 expression occur rapidly in hepatocytes stimulated to proliferate and that several nonparenchymal liver cell types upregulate Cx43 expression when induced to proliferate. Differentiation of oval cells into basophilic hepatocytes resulted in their expression of Cx32 and Cx26.
Authors:
M J Neveu; J R Hully; K L Babcock; J Vaughan; E L Hertzberg; B J Nicholson; D L Paul; H C Pitot
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Publication Detail:
Type:  Comparative Study; 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:  22     ISSN:  0270-9139     ISO Abbreviation:  Hepatology     Publication Date:  1995 Jul 
Date Detail:
Created Date:  1995-08-09     Completed Date:  1995-08-09     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  8302946     Medline TA:  Hepatology     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  202-12     Citation Subset:  IM    
Affiliation:
Pfizer Central Research, Groton, CT, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Blotting, Northern
Cell Division
Connexins / genetics,  metabolism
Female
Gap Junctions / genetics,  physiology*
Gene Expression*
Hepatectomy / methods
Immunohistochemistry
Liver / cytology*,  physiology*
RNA, Messenger / metabolism
Rats
Rats, Inbred F344
Rats, Sprague-Dawley
Time Factors
Grant Support
ID/Acronym/Agency:
CA-07175/CA/NCI NIH HHS; CA-22484/CA/NCI NIH HHS; CA-45700/CA/NCI NIH HHS
Chemical
Reg. No./Substance:
0/Connexins; 0/RNA, Messenger

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


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