Document Detail


Effect of cell density on metabolism in isolated rat hepatocytes.
MedLine Citation:
PMID:  3988816     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Freshly isolated rat hepatocytes show many changes in metabolic activities as a function of cell density in the incubation flask. Fatty acid synthesis, cholesterol synthesis, general protein synthesis, and rates of accumulation of pyruvate, lactate, citrate, acetyl-CoA, acetoacetate and beta-hydroxybutyrate decrease as the cell density increases between 1 mg/ml and 60 mg/ml. Glucose release only decreases between 1-5 mg/ml and the concentration of ATP does not vary at any density. There is a small increase in the lactate/pyruvate ratio and a dramatic decrease in the beta-hydroxybutyrate/acetoacetate ratio with increasing cell concentration. When cells at 8 or 28 mg/ml were incubated with added lactate and pyruvate, or alanine, a two fold increase in fatty acid synthesis and 50% decrease in cholesterol synthesis were observed as compared to rates with endogenous substrate. With added glucose the synthetic rates were similar to those obtained with endogenous substrate. However, regardless of the type of substrate used, the less dense cells gave rates up to three times greater than that of the more dense cells. When conditioned medium isolated after incubation of cells at high density was added to the less dense cells, a decrease in the rates of fatty acid synthesis and cholesterol synthesis was observed in the less dense cells; however, when medium from the less dense cells after incubation for the same period was added to the more dense cells, there was no significant change in fatty acid or cholesterol synthesis. These results suggest that a factor may be released into the medium of incubating hepatocytes that progressively inhibits certain metabolic processes as the cell density increases.
Authors:
R R Jurin; S A McCune
Related Documents :
9409206 - Role of activin-a and follistatin in foam cell formation of thp-1 macrophages.
1252356 - Incorporation of i-14c-acetate into the lipids of isolated epidermal cells.
1247506 - Complete retention of phospholipid acyl groups by mammalian cells in culture.
1689566 - Intracellular lipid droplets in functioning transitional parathyroid oxyphil adenomas. ...
7765586 - Mass spectrometry: a tool for on-line monitoring of animal cell cultures.
12408376 - Cyclooxygenase inhibitors block cell growth, increase ceramide and inhibit cell cycle.
Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Journal of cellular physiology     Volume:  123     ISSN:  0021-9541     ISO Abbreviation:  J. Cell. Physiol.     Publication Date:  1985 Jun 
Date Detail:
Created Date:  1985-06-19     Completed Date:  1985-06-19     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  0050222     Medline TA:  J Cell Physiol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  442-8     Citation Subset:  IM    
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adenosine / pharmacology
Adenosine Triphosphate / metabolism
Animals
Cell Count
Cholesterol / metabolism
Fatty Acids / metabolism
Lactates / metabolism
Liver / cytology,  metabolism*
Oleic Acid
Oleic Acids / pharmacology
Protein Biosynthesis
Pyruvates / metabolism
Rats
Grant Support
ID/Acronym/Agency:
AM 30979/AM/NIADDK NIH HHS; BRSG-RR05366/RR/NCRR NIH HHS
Chemical
Reg. No./Substance:
0/Fatty Acids; 0/Lactates; 0/Oleic Acids; 0/Pyruvates; 112-80-1/Oleic Acid; 56-65-5/Adenosine Triphosphate; 57-88-5/Cholesterol; 58-61-7/Adenosine

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


Previous Document:  Characterization of mouse lymphoma cells with altered nucleoside transport.
Next Document:  Metabolic properties of an azaguanine-resistant variant of Chinese hamster ovary cells (azarts) with...