A GATA-specific inhibitor (K-7174) rescues anemia induced by IL-1beta, TNF-alpha, or L-NMMA

FASEB J. 2003 Sep;17(12):1742-4. doi: 10.1096/fj.02-1134fje. Epub 2003 Jul 18.

Abstract

Interleukin-1beta (IL-1beta), tumor necrosis factor-alpha (TNF-alpha), or N(G)-monomethyl-L-arginine (L-NMMA) are increased in patients with chronic disease-related anemia. They increase the binding activity of GATA and inhibit erythropoietin (Epo) promoter activity. In this study, we examined the ability of K-7174 (a GATA-specific inhibitor) to improve Epo production when inhibited by treatment with IL-1beta, TNF-alpha, or L-NMMA. Epo protein production and promoter activity were induced in Hep3B cells with 1% O2. However, 15 U/ml IL-1beta, 220 U/ml TNF-alpha, or 10(-3) M L-NMMA inhibited Epo protein production and promoter activity, respectively. Addition of 10 microM K-7174 rescued these inhibitions of Epo protein production and promoter activity induced by IL-1beta, TNF-alpha, or L-NMMA, respectively. Electrophoretic mobility shift assays revealed that addition of K-7174 decreased GATA binding activity, which was increased with the addition of IL-1beta, TNF-alpha, or L-NMMA. Furthermore, intraperitoneal injection of mice with IL-1beta or TNF-alpha decreased the hemoglobin concentrations and reticulocyte counts. However, the addition of K-7174 reversed these effects. These results raise the possibility of using K-7174 as therapy to treat anemia.

MeSH terms

  • Anemia / chemically induced
  • Anemia / drug therapy*
  • Anemia / metabolism
  • Animals
  • Anisoles / pharmacology
  • Anisoles / therapeutic use*
  • Azepines / pharmacology
  • Azepines / therapeutic use*
  • Binding Sites
  • Cell Count
  • Cell Hypoxia
  • Cell Line
  • DNA-Binding Proteins / antagonists & inhibitors*
  • DNA-Binding Proteins / metabolism
  • Erythropoietin / biosynthesis
  • Erythropoietin / genetics
  • Hemoglobins / analysis
  • Interleukin-1 / antagonists & inhibitors
  • Mice
  • Models, Genetic
  • Promoter Regions, Genetic
  • Reticulocytes / cytology
  • Transcription Factors / antagonists & inhibitors*
  • Transcription Factors / metabolism
  • Transcriptional Activation
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • omega-N-Methylarginine / antagonists & inhibitors

Substances

  • Anisoles
  • Azepines
  • DNA-Binding Proteins
  • Hemoglobins
  • Interleukin-1
  • Transcription Factors
  • Tumor Necrosis Factor-alpha
  • Erythropoietin
  • omega-N-Methylarginine
  • K 7174