The heat shock response inhibits RANTES gene expression in cultured human lung epithelium

J Immunol. 1998 Sep 1;161(5):2594-9.

Abstract

The chemokine RANTES is thought to be involved in the pathophysiology of inflammation-associated acute lung injury. Although much is known regarding signals that induce RANTES gene expression, relatively few data exist regarding signals that inhibit RANTES gene expression. The heat shock response, a highly conserved cellular defense mechanism, has been demonstrated to inhibit a variety of lung proinflammatory responses. We tested the hypothesis that induction of the heat shock response inhibits RANTES gene expression. Treatment of A549 cells with TNF-alpha induced RANTES gene expression in a concentration-dependent manner. Induction of the heat shock response inhibited subsequent TNF-alpha-mediated RANTES mRNA expression and secretion of immunoreactive RANTES. Transient transfection assays involving a RANTES promoter-luciferase reporter plasmid demonstrated that the heat shock response inhibited TNF-alpha-mediated activation of the RANTES promoter. Inhibition of NF-kappaB nuclear translocation with isohelenin inhibited TNF-alpha-mediated RANTES mRNA expression, indicating that RANTES gene expression is NF-kappaB dependent in A549 cells. Induction of the heat shock response inhibited degradation of the NF-kappaB inhibitory protein, I-kappaBalpha but did not significantly inhibit phosphorylation of I-kappaBalpha. We conclude that the heat shock response inhibits RANTES gene expression by a mechanism involving inhibition of NF-kappaB nuclear translocation and subsequent inhibition of RANTES promoter activation. The mechanism by which the heat shock response inhibits NF-kappaB nuclear translocation involves stabilization of I-kappaBalpha, without significantly affecting phosphorylation of I-kappaBalpha.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenocarcinoma
  • Chemokine CCL5 / antagonists & inhibitors
  • Chemokine CCL5 / genetics*
  • Chemokine CCL5 / metabolism
  • DNA-Binding Proteins / metabolism
  • Epithelial Cells / metabolism*
  • Gene Expression Regulation, Neoplastic*
  • Heat-Shock Response / genetics*
  • Humans
  • I-kappa B Proteins*
  • Lung / metabolism*
  • Lung Neoplasms
  • NF-KappaB Inhibitor alpha
  • NF-kappa B / antagonists & inhibitors
  • Phosphorylation
  • Promoter Regions, Genetic
  • RNA, Messenger / biosynthesis
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / physiology

Substances

  • Chemokine CCL5
  • DNA-Binding Proteins
  • I-kappa B Proteins
  • NF-kappa B
  • NFKBIA protein, human
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • NF-KappaB Inhibitor alpha