Abstract

Polycyclic aromatic hydrocarbons such as 3-methylcholanthrene are toxic to rat epidermal cells in low passages (3 to 6), but cultures of high passage (>/=15) are resistant. Since such compounds can be metabolically activated by cytochrome P4501A1, we have examined the regulation of this gene in low and high passage cells. Consistent with this difference, little or no 2,3,7, 8-tetrachlorodibenzo-p-dioxin (TCDD)-inducible P4501A1 mRNA or enzyme activity was observed in high passage as compared to low passage cultures. Similarly, transfection of a luciferase reporter construct containing -1317 to +256 base pairs of the 5'-flanking region of the murine CYP1A1 gene was TCDD-inducible in low but not high passage cells. Ligand binding and transfection experiments demonstrated the presence of functional Ah receptor complexes in both high and low passage cells. Deletion analysis identified a 26-base pair negative regulatory DNA (NeRD) element contained within the upstream regulatory region of the CYP1A1 gene responsible for this effect. Nuclear extracts from both low and high passage cells contain a protein which specifically binds to NeRD-containing DNA. Thus, the loss of polycyclic aromatic hydrocarbon sensitivity in high passage rat epidermal cells appears to be due to decreased expression of CYP1A1, and this effect may be mediated by an altered NeRD binding factor(s) present in these cells.

Highlights

  • Polycyclic aromatic hydrocarbons (PAHs) induce cytochrome P4501A1 and are metabolized by this enzyme to DNA-damaging electrophiles that lead to mutations and cellular transformation [3]

  • The loss of Aryl Hydrocarbon Hydroxylase (AHH) activity in high passage rat epidermal cells appears to be due to a dramatic reduction in inducible cyto

  • The inability of transformed Ah receptor (AhR) complex to bind to the dioxin responsive element (DRE) prevents inducible expression of the CYP1A1 gene

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Summary

Numerous biochemical studies have demonstrated that

PAHs induce cytochrome P4501A1 and are metabolized by this enzyme to DNA-damaging electrophiles that lead to mutations and cellular transformation [3]. The induction of cytochrome P4501A1 by PAHs and related chemicals such as 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD, dioxin) is mediated by the Ah receptor (AhR), a ligand dependent, DNA-regulatory protein to which these chemicals bind with high affinity (4 – 8). Previous studies of murine and human epidermal keratinocytes have demonstrated that PAH responsiveness (CYP1A1 inducibility) is dependent upon the differentiated state of the cells, with those committed to terminal differentiation being most responsive (28 –31). The mechanistic basis for the differentiation-dependent change in PAH responsiveness is currently unknown It is not clear whether the spontaneous loss of PAH responsiveness in high passage rat keratinocytes is related to their loss of differentiated phenotype, the availability of a variety of molecular probes to the CYP1A1 system allows us to examine the mechanism of the spontaneous loss of PAH sensitivity in rat epidermal cells in detail. Transfection and deletion analysis have identified a novel cis-acting negative regulatory DNA (NeRD) element present upstream of the CYP1A1 promoter that acts to negatively regulate TCDDinducible expression of the CYP1A1 gene in HP cells

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