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J. Biol. Chem., Vol. 263, Issue 24, 11802-11807, Aug, 1988
G Silver and KS Krauter
Primary cultures of adult rat hepatocytes grown in serum-free hormonally
defined medium were shown, for the first time, to be capable of supporting
the 3-methylcholanthrene-inducible expression of cytochrome P-450d. Such
cultures were used to investigate the mechanism of the induction of
cytochrome P-450c and P-450d mRNAs. After 1 day of growth in culture,
P-450c and P-450d mRNAs were induced 33- and 28- fold, respectively, by
3-methylcholanthrene treatment. A similar magnitude of induction was
achieved after 2-5 days growth in culture. However, the relative abundance
of the two mRNAs before and after treatment decreased linearly over the
5-day time course. Kinetic analysis revealed that induction of both genes
was rapid and could be observed less than 2 h following treatment.
Accumulation of both mRNAs was linear for 8 h, reaching a plateau by 12 h.
Expression then remained constant for at least 12 additional hours. In
vitro nuclear run-on experiments revealed a 3.9- and 2.0-fold
transcriptional induction of the P-450c and P-450d genes, respectively.
This is in contrast to the large induction of accumulation of these mRNAs
observed at steady state. Thus, the 3-methylcholanthrene induction of
P-450c and P-450d mRNAs in the hepatocyte cultures appeared to be mediated
primarily at the post-transcriptional level. Experiments on rat liver
showed that, in vivo, P-450d is also regulated primarily at the post-
transcriptional level. However, P-450c was found to be regulated primarily
transcriptionally.
Expression of cytochromes P-450c and P-450d mRNAs in cultured rat hepatocytes. 3-Methylcholanthrene induction is regulated primarily at the post-transcriptional level
Department of Cell Biology, Albert Einstein College of Medicine, Bronx, New York 10461.
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