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Correlation between the expression level of c-maf and glutathione peroxidase-3 in c-maf -/- mice kidney and c-maf overexpressed renal tubular cells
被引:13
作者:
Shirota, S.
Yoshida, T.
Sakai, M.
Kim, J. I.
Sugiura, H.
Oishi, T.
Nitta, K.
Tsuchiya, K.
机构:
[1] Tokyo Womens Med Univ, Dept Med 4, Shinjuku Ku, Tokyo 1628666, Japan
[2] Hokkaido Univ, Sch Med, Dept Hlth Sci, Kita Ku, Sapporo, Hokkaido 0600812, Japan
[3] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
关键词:
glutathione peroxidase-3;
IMCD cell;
maf;
microarray;
oxidative stress;
transcriptional factor;
D O I:
10.1016/j.bbrc.2006.07.111
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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. (c) 2006 Elsevier Inc. All rights reserved.
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页码:501 / 506
页数:6
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