Abstract
To investigate the role of newly synthesized apocytochrome P450 (P450) in the regulation of 5-aminolevulinate synthase (ALAS), we overexpressed P450 in primary cultures of chick embryo hepatocytes and measured the subsequent effects on ALAS mRNA by semiquantitative RT-PCR. Hepatocytes were co-transfected with a vector for expression of P450 cDNAs (CYP3A4 or CYP2H1) and a vector directing the synthesis of a cell surface antibody. Transfected hepatocytes were isolated with hapten-coated magnetic beads at different times after electroporation (4, 8 and 20 h). Overexpression of human CYP3A4 was demonstrated by high levels of the corresponding mRNA and apoprotein as analyzed by RT-PCR and western-blot analysis. Similarly, chicken CYP2H1 was expressed to levels even higher than those induced with phenobarbital. However the level of ALAS mRNA did not change in these cells. Our results demonstrate that the induction of ALAS by drugs is not a direct consequence of increased P450 apoprotein synthesis and heme utilization.
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