Serum after partial hepatectomy stimulates iNOS gene transcription via downstream NF-kappa B site

Biochem Biophys Res Commun. 2001 Jun 15;284(3):607-13. doi: 10.1006/bbrc.2001.5034.

Abstract

It has been known that the expression of inducible nitric oxide synthase (iNOS) is up-regulated during hepatic regeneration. The present study characterized the molecular mechanisms involved in the transcriptional activation of iNOS gene by using the serum after partial hepatectomy (post-PH serum) in vitro. The post-PH serum rapidly induced iNOS mRNA expression, which was blocked by anti-tumor necrosis factor-alpha (TNF-alpha) antibody in BNL CL.2 cells, murine embryonic liver cell line. In addition, EMSAs using a NF-kappa B-specific oligomer showed that the up-regulated iNOS mRNA expression in cells treated with post-PH serum correlated with transient activation of NF-kappa B complex (p50/p65 heterodimer). Transient transfection of BNL CL.2 cells with iNOS promoter linked to a CAT reporter gene showed the transcriptional activation of iNOS promoter by post-PH serum. Furthermore, site-directed mutational analysis of the two NF-kappa B sites individually or in combination revealed that iNOS expression by post-PH serum is regulated by the downstream NF-kappa B site, but not by upstream NF-kappa B site. Taken together, these results suggest that the downstream NF-kappa B site acts as an essential component for the iNOS expression by post-PH serum during hepatic regeneration.

MeSH terms

  • Animals
  • Antibodies / immunology
  • Blood*
  • Cell Line
  • Culture Media
  • Hepatectomy*
  • Kinetics
  • Liver Regeneration
  • Mice
  • NF-kappa B / metabolism*
  • Nitric Oxide Synthase / biosynthesis
  • Nitric Oxide Synthase / genetics*
  • Nitric Oxide Synthase Type II
  • Promoter Regions, Genetic
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Sprague-Dawley
  • Response Elements
  • Transcriptional Activation
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • Antibodies
  • Culture Media
  • NF-kappa B
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Nitric Oxide Synthase
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse
  • Nos2 protein, rat