Expression of stably transfected murine glutathione S-transferase A3-3 protects against nucleic acid alkylation and cytotoxicity by aflatoxin B-1 in hamster V79 cells expressing rat cytochrome P450-2B1

Aflatoxin B-1 (AFB(1)) is activated to AFB(1)-8,9-oxide (AFBO), a potent mu tagenic and carcinogenic metabolite of AFB(1), In the mouse, AFBO has been shown to be most efficiently detoxified by a specific isozyme of alpha-clas s glutathione S-transferase (GST), mGSTA3-3 (mGST-Yc), A hamster V79 cell l ine (V79MZr2B1, originally designated V79/SD1) previously transfected with the rat cytochrome P450-2B1 was stably transfected with an mGSTA3-3 express ion vector, to study the chemopreventive role of GST in protecting against cytotoxicity or genotoxicity of AFBO, Immunoblotting demonstrated strong ex pression of an alpha-class GST in the mGSTA3-3 transfected cell line, where as no detectable alpha-class GST protein was observed in the control (empty vector-transfected) cells, Previous studies with the V79MZr2B1 cell line i ndicated that it can activate AFB(1) to a mutagenic metabolite via a transf ected rat P450-2B1 stably expressed in the cells. We examined the ability o f the expressed mGSTA3-3 to protect against AFB(1)-induced cytotoxicity or [H-3]-covalent adduct formation in cellular nucleic acids. Exposure of empt y vector-transfected control cells and mGSTA3-3 expressing cells to up to 6 00 nM [H-3]-AFB(1) indicated that a 70-80% reduction in DNA and RNA adducts was afforded by the expression of mGSTA3-3 in the transfected cells. Clono genic survival assays showed that the mGSTA3-3 cell line was 4.6-fold resis tant to AFB(1) cytotoxicity as compared with the empty vector-transfected c ontrol SD1 cells, with IC50 values of 69 and 15 mu M, respectively. The res ults of these studies demonstrate that mGSTA3-3 confers substantial protect ion against nucleic acid covalent modification and cytotoxicity by AFB(1) i n this transgenic cell model system.