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Cell‐density‐dependent Expression of Cyp1a2 Gene in Monolayer‐cultured Adult Mouse Hepatocytes

Expression of Cyp1a1 and Cyp1a2 genes was investigated in adult C57BL/6NCrj mouse hepatocytes for up to 5 days after transfer to monolayer culture. CYP1A1 mRNA was substantially induced by treatment with 3‐methylcholanthrene during the observation period, independently of the seeded cell density. Ho...

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Detalles Bibliográficos
Autores principales: Nemoto, Nobuo, Sakurai, Junko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1993
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919153/
https://www.ncbi.nlm.nih.gov/pubmed/8486527
http://dx.doi.org/10.1111/j.1349-7006.1993.tb02866.x
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author Nemoto, Nobuo
Sakurai, Junko
author_facet Nemoto, Nobuo
Sakurai, Junko
author_sort Nemoto, Nobuo
collection PubMed
description Expression of Cyp1a1 and Cyp1a2 genes was investigated in adult C57BL/6NCrj mouse hepatocytes for up to 5 days after transfer to monolayer culture. CYP1A1 mRNA was substantially induced by treatment with 3‐methylcholanthrene during the observation period, independently of the seeded cell density. However, expression of CYP1A2 mRNA was dependent on cell density and was higher in cells cultivated at lower density. With increasing culture period the expression was decreased, so that only negligible levels were evident by day 5, and reduced expression of constitutive and induced CYP1A2 mRNA became apparent earlier in more densely seeded cells. This was not related to differences in numbers of inducer molecules per cell. While mouse hepatocytes incorporated tritium‐labeled thymidine under the given culture conditions, induction of expression of the two Cyp1a genes did not show any direct relationship with DNA synthesizing activity. These observations suggest some role for Cyp1a2 during changes in physiological state.
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spelling pubmed-59191532018-05-11 Cell‐density‐dependent Expression of Cyp1a2 Gene in Monolayer‐cultured Adult Mouse Hepatocytes Nemoto, Nobuo Sakurai, Junko Jpn J Cancer Res Article Expression of Cyp1a1 and Cyp1a2 genes was investigated in adult C57BL/6NCrj mouse hepatocytes for up to 5 days after transfer to monolayer culture. CYP1A1 mRNA was substantially induced by treatment with 3‐methylcholanthrene during the observation period, independently of the seeded cell density. However, expression of CYP1A2 mRNA was dependent on cell density and was higher in cells cultivated at lower density. With increasing culture period the expression was decreased, so that only negligible levels were evident by day 5, and reduced expression of constitutive and induced CYP1A2 mRNA became apparent earlier in more densely seeded cells. This was not related to differences in numbers of inducer molecules per cell. While mouse hepatocytes incorporated tritium‐labeled thymidine under the given culture conditions, induction of expression of the two Cyp1a genes did not show any direct relationship with DNA synthesizing activity. These observations suggest some role for Cyp1a2 during changes in physiological state. Blackwell Publishing Ltd 1993-03 /pmc/articles/PMC5919153/ /pubmed/8486527 http://dx.doi.org/10.1111/j.1349-7006.1993.tb02866.x Text en
spellingShingle Article
Nemoto, Nobuo
Sakurai, Junko
Cell‐density‐dependent Expression of Cyp1a2 Gene in Monolayer‐cultured Adult Mouse Hepatocytes
title Cell‐density‐dependent Expression of Cyp1a2 Gene in Monolayer‐cultured Adult Mouse Hepatocytes
title_full Cell‐density‐dependent Expression of Cyp1a2 Gene in Monolayer‐cultured Adult Mouse Hepatocytes
title_fullStr Cell‐density‐dependent Expression of Cyp1a2 Gene in Monolayer‐cultured Adult Mouse Hepatocytes
title_full_unstemmed Cell‐density‐dependent Expression of Cyp1a2 Gene in Monolayer‐cultured Adult Mouse Hepatocytes
title_short Cell‐density‐dependent Expression of Cyp1a2 Gene in Monolayer‐cultured Adult Mouse Hepatocytes
title_sort cell‐density‐dependent expression of cyp1a2 gene in monolayer‐cultured adult mouse hepatocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919153/
https://www.ncbi.nlm.nih.gov/pubmed/8486527
http://dx.doi.org/10.1111/j.1349-7006.1993.tb02866.x
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