TY - JOUR
T1 - Suppression of erythropoietin gene expression by cadmium depends on inhibition of HIF-1, not stimulation of GATA-2
AU - Obara, Naoshi
AU - Imagawa, Shigehiko
AU - Nakano, Yoko
AU - Suzuki, Norio
AU - Yamamoto, Masayuki
AU - Nagasawa, Toshiro
N1 - Funding Information:
Acknowledgements We thank Hiromi Tanaka and Ayako Hoshino for their expert technical assistance. This work was supported by Grants-in-aid for scientific research from the Ministry of Education, Science and Culture of Japan, and the Renal Anemia Foundation, Japan.
PY - 2003/5/1
Y1 - 2003/5/1
N2 - Long-term exposure of rats to cadmium (Cd) resulted in a marked suppression of erythropoietin (Epo) mRNA expression in the kidneys and the development of severe anemia. A recent report revealed that Cd inhibited hypoxia-inducible factor 1 (HIF-1) binding activity and Epo mRNA expression and protein production. However, Epo gene expression is also regulated by transcription factor GATA-2, which binds to the GATA binding site of the Epo promoter. To elucidate the mechanism of suppression of Epo by Cd, the effect of Cd on GATA-2 function was studied. Epo promoter/enhancer luciferase constructs, one with the wild-type promoter and another with a promoter with a mutant GATA site, were transfected into Hep3B zcells. No significant difference in Epo promoter activity in these two types of cells was observed in the presence of Cd. The binding activity of GATA-2 was not affected by Cd. This study showed that Cd inhibited HIF-1 binding activity and Epo promoter activity, and then suppressed Epo protein production. Inhibition of Epo gene expression by Cd depends on suppression of HIF-1 binding activity, not on alteration of GATA function.
AB - Long-term exposure of rats to cadmium (Cd) resulted in a marked suppression of erythropoietin (Epo) mRNA expression in the kidneys and the development of severe anemia. A recent report revealed that Cd inhibited hypoxia-inducible factor 1 (HIF-1) binding activity and Epo mRNA expression and protein production. However, Epo gene expression is also regulated by transcription factor GATA-2, which binds to the GATA binding site of the Epo promoter. To elucidate the mechanism of suppression of Epo by Cd, the effect of Cd on GATA-2 function was studied. Epo promoter/enhancer luciferase constructs, one with the wild-type promoter and another with a promoter with a mutant GATA site, were transfected into Hep3B zcells. No significant difference in Epo promoter activity in these two types of cells was observed in the presence of Cd. The binding activity of GATA-2 was not affected by Cd. This study showed that Cd inhibited HIF-1 binding activity and Epo promoter activity, and then suppressed Epo protein production. Inhibition of Epo gene expression by Cd depends on suppression of HIF-1 binding activity, not on alteration of GATA function.
KW - Cadmium
KW - Erythropoietin
KW - GATA
KW - Hypoxia-inducible factor 1α
KW - Transcriptional regulation
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U2 - 10.1007/s00204-003-0444-0
DO - 10.1007/s00204-003-0444-0
M3 - Article
C2 - 12734640
AN - SCOPUS:0038470877
SN - 0340-5761
VL - 77
SP - 267
EP - 273
JO - Archives of Toxicology
JF - Archives of Toxicology
IS - 5
ER -