Padgham C R, Paine A J, Phillips I R, Shephard E A
DH Department of Toxicology, St. Bartholomew's Hospital Medical College, London, U.K.
Biochem J. 1992 Aug 1;285 ( Pt 3)(Pt 3):929-32. doi: 10.1042/bj2850929.
mRNAs encoding cytochrome P-450s CYP1A2 and CYP2B1/2 have been quantified in rat hepatocytes cultured for periods up to 72 h under several different culture conditions that maintain total cytochrome P-450 content. When hepatocytes were cultured at either 37 or 30 degrees C in Williams E media, both CYP1A2 and CYP2B1/2 mRNAs declined dramatically. However, when cultured at 30 degrees C for 24 h, the decline in these mRNAs was not as great as that observed in cells grown at 37 degrees C. The addition of dimethyl sulphoxide to cells grown at 37 degrees C did not affect the rate of disappearance of the CYP1A2 or CYP2B1/2 mRNAs. These mRNAs also declined rapidly in cells grown in 'P-450 medium' i.e. RPMI 1640 medium without cyst(e)ine but supplemented with 0.1 mM-delta-aminolaevulinic acid. However, the levels of CYP2B1/2 mRNAs were maintained when hepatocytes were cultured in Williams E medium supplemented with 0.5 mM-metyrapone. These conditions did not, however, maintain the levels of CYP1A2 mRNA.
在几种维持细胞色素P - 450总含量的不同培养条件下,对培养长达72小时的大鼠肝细胞中编码细胞色素P - 450的CYP1A2和CYP2B1/2的mRNA进行了定量分析。当肝细胞在Williams E培养基中于37或30℃培养时,CYP1A2和CYP2B1/2的mRNA均显著下降。然而,当在30℃培养24小时时,这些mRNA的下降幅度不如在37℃培养的细胞中观察到的大。向在37℃培养的细胞中添加二甲基亚砜并不影响CYP1A2或CYP2B1/2的mRNA消失速率。在“P - 450培养基”(即不含胱氨酸但补充有0.1 mM - δ - 氨基乙酰丙酸的RPMI 1640培养基)中培养的细胞中,这些mRNA也迅速下降。然而,当肝细胞在补充有0.5 mM - 美替拉酮的Williams E培养基中培养时,CYP2B1/2的mRNA水平得以维持。然而,这些条件并未维持CYP1A2 mRNA的水平。