Silver G, Krauter K S
Department of Cell Biology, Albert Einstein College of Medicine, Bronx, New York 10461.
J Biol Chem. 1988 Aug 25;263(24):11802-7.
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.
首次发现,在无血清激素限定培养基中培养的成年大鼠肝细胞原代培养物能够支持细胞色素P-450d的3-甲基胆蒽诱导表达。此类培养物用于研究细胞色素P-450c和P-450d mRNA的诱导机制。在培养1天后,经3-甲基胆蒽处理,P-450c和P-450d mRNA分别诱导了33倍和28倍。在培养2 - 5天后也实现了类似程度的诱导。然而,在5天的时间进程中,处理前后两种mRNA的相对丰度呈线性下降。动力学分析表明,两个基因的诱导都很快,在处理后不到2小时即可观察到。两种mRNA的积累在8小时内呈线性,到12小时达到平台期。然后表达至少在另外12小时内保持恒定。体外细胞核连续转录实验表明,P-450c和P-450d基因的转录分别诱导了3.9倍和2.0倍。这与在稳态时观察到的这些mRNA积累的大量诱导形成对比。因此,肝细胞培养物中3-甲基胆蒽对P-450c和P-450d mRNA的诱导似乎主要在转录后水平介导。对大鼠肝脏的实验表明,在体内,P-450d也主要在转录后水平受到调节。然而,发现P-450c主要在转录水平受到调节。