RT Journal Article
SR Electronic
T1 Activation of <em>c-Ha-ras </em>by Benzo(<em>a</em>)pyrene in Vascular Smooth Muscle Cells Involves Redox Stress and Aryl Hydrocarbon Receptor
JF Molecular Pharmacology
JO Mol Pharmacol
FD American Society for Pharmacology and Experimental Therapeutics
SP 152
OP 158
DO 10.1124/mol.58.1.152
VO 58
IS 1
A1 J. Kevin Kerzee
A1 Kenneth S. Ramos
YR 2000
UL http://molpharm.aspetjournals.org/content/58/1/152.abstract
AB Repeated cycles of vascular injury by benzo(a)pyrene (BaP) increase the onset and progression of atherosclerotic lesions in laboratory animals. This atherogenic response is partly mediated by activation of cis-acting antioxidant/electrophile response elements that enhance c-Ha-ras transcription in vascular smooth muscle cells (vSMCs). Activation of antioxidant/electrophile responsive cis-acting elements may depend on metabolism of BaP by cytochrome P450s to intermediates that induce oxidative stress and modulate gene expression. To test this hypothesis, we evaluated mitogen-activated c-Ha-ras expression in vSMCs treated with BaP or its metabolic intermediates alone, and in combination with agents that modulate cellular redox status. BaP (0.3 and 3 μM), BaP-3,6-quinone (0.3 μM), or hydrogen peroxide (50 μM) enhanced serum-activated c-Ha-ras. Ellipticine (0.01 nM), a known inhibitor of cytochrome P450 metabolism and aryl hydrocarbon receptor (AhR) antagonist, inhibitedc-Ha-ras induction by BaP (3 μM). Serum challenge of G0 synchronized cultures of vSMCs withdl-buthionine-(S,R)-sulfoximine (0.1 mM), a depletor of cellular glutathione, increasedc-Ha-ras mRNA levels during the early phase of the mitogenic response. Combined BaP/dl-buthionine-(S,R)-sulfoximine challenge was cytotoxic to the cells and inhibitedc-Ha-ras expression, whereas up-regulation of antioxidant capacity by N-acetylcysteine (0.5 mM) precluded BaP-induced ras expression. BaP increased formation of reactive oxygen species and depleted cellular glutathione, but these changes did not correlate with the kinetics ofc-Ha-ras induction. BaP did not enhancec-Ha-ras expression in vSMCs from AhR knockout mice, although aryl hydrocarbon hydroxylase activity was constitutively expressed in these cells. These results suggest thatc-Ha-ras activation in vSMCs by BaP involves a redox-sensitive mechanism that is coupled to AhR receptor-dependent functions.