Involvement of CCAAT/enhancer-binding protein alpha in haptoglobin gene expression by all-trans-retinoic acid

Biochem Biophys Res Commun. 2002 Jun 28;294(5):956-61. doi: 10.1016/S0006-291X(02)00581-8.

Abstract

Several acute-phase plasma proteins, including haptoglobin (Hp), are induced in the liver in response to inflammation. Recently, we found that Hp gene expression is up-regulated by all-trans-retinoic acid (ATRA) in the extrahepatic monocytic cell line, THP-1. To investigate the molecular mechanism underlying ATRA-induced Hp gene expression, we analyzed the induction of transcription factor CCAAT/enhancer-binding protein (C/EBP) isoforms in ATRA-stimulated THP-1 cells and their binding to the Hp promoter. Western blot analysis showed that treatment with ATRA increased C/EBPalpha and beta expression, but decreased that of C/EBPdelta. Electrophoretic mobility shift and supershift assays demonstrated that only C/EBPalpha of the C/EBP isoforms bound to the C/EBP DNA-binding sites in the Hp promoter. Furthermore, when ATRA-dependent Hp induction was inhibited by sodium butyrate or auranofin, induction of C/EBPalpha, but not C/EBPbeta, was also diminished. These results suggest that C/EBPalpha is involved in the activation of Hp gene expression by ATRA in human monocytic cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Inflammatory Agents / pharmacology
  • CCAAT-Enhancer-Binding Protein-alpha / physiology*
  • Cell Line
  • Haptoglobins / biosynthesis
  • Haptoglobins / genetics*
  • Humans
  • Interleukin-6 / pharmacology
  • Monocytes / drug effects
  • Monocytes / metabolism*
  • Promoter Regions, Genetic
  • Protein Isoforms / biosynthesis
  • RNA, Messenger / biosynthesis
  • Transcriptional Activation*
  • Tretinoin / pharmacology*
  • Tumor Cells, Cultured

Substances

  • Anti-Inflammatory Agents
  • CCAAT-Enhancer-Binding Protein-alpha
  • Haptoglobins
  • Interleukin-6
  • Protein Isoforms
  • RNA, Messenger
  • Tretinoin