
pmid: 16890189
Large mafs are transcriptional factors and members of the basic leucine zipper (b-Zip) superfamily. Since we previously identified expression of c-maf in mouse kidney, we presently investigated the mRNA expression profile in the kidney of c-maf gene knockout mice by using DNA microarray, and plasma glutathione peroxidase-3 (GPx3) was predominantly downregulated. We focused on the relation between the expression level of c-maf and GPx3 in vivo and in vitro. Since GPx3 is an antioxidant enzyme, oxidative stress was induced by exposing a culture cell derived from mouse renal tubules (mIMCD3) to hydrogen peroxide. Real-time PCR demonstrated that mRNA expression of both c-maf and GPx3 increased in parallel during exposure to oxidative stress in a time- and dose-dependent manner. Then, the mIMCD3 cells were transfected with c-maf-cDNA containing plasmid, which resulted in an increase in mRNA and protein expression of GPx3 compared with the control cells. Thus, c-maf may be transcriptional regulator of GPx3 expression and modulate the antioxidative pathway in the kidney.
Mice, Knockout, Glutathione Peroxidase, Gene Expression Profiling, Hydrogen Peroxide, Kidney, Mice, Oxidative Stress, Kidney Tubules, Proto-Oncogene Proteins c-maf, Animals, Cells, Cultured
Mice, Knockout, Glutathione Peroxidase, Gene Expression Profiling, Hydrogen Peroxide, Kidney, Mice, Oxidative Stress, Kidney Tubules, Proto-Oncogene Proteins c-maf, Animals, Cells, Cultured
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