The Th2 cell cytokines IL-4 and IL-13 regulate found in inflammatory zone 1/resistin-like molecule alpha gene expression by a STAT6 and CCAAT/enhancer-binding protein-dependent mechanism

J Immunol. 2003 Feb 15;170(4):1789-96. doi: 10.4049/jimmunol.170.4.1789.

Abstract

The onset of allergic inflammation in the lung is driven by a complex genetic program. This study shows that found in inflammatory zone (FIZZ)1 and FIZZ2, but not FIZZ3, gene expression was up-regulated 6 h after Ag challenge in a mouse model of acute pulmonary inflammation. Induction of both genes was abolished in allergen-challenged STAT6-deficient mice. FIZZ1, but not FIZZ2, mRNA was up-regulated upon incubation of the myeloid cell line BMnot with IL-4. The promoter region of FIZZ1 contains functional binding sites for STAT6 and C/EBP. FIZZ1 promoter reporter gene constructs responded to IL-4 and IL-13 stimulation in transiently transfected cells. Point mutations in the STAT6 or the C/EBP site led to loss of cytokine responsiveness indicating that IL-4-mediated induction of murine FIZZ1 is orchestrated by the coordinate action of STAT6 and C/EBP. It is concluded that the expression of the genes encoding FIZZ1 and FIZZ2, but not FIZZ3, is induced in allergen-challenged lungs in a STAT6-dependent fashion. STAT6 directly regulates IL-4- and IL-13-triggered induction of FIZZ1 expression at the transcriptional level by cooperation with C/EBP. Induction of FIZZ2 gene expression most likely occurs independent of a direct effect by these cytokines and may be due to indirect STAT6-driven mechanisms.

MeSH terms

  • Animals
  • Antigens / administration & dosage
  • Base Sequence
  • Binding Sites / genetics
  • Binding Sites / immunology
  • CCAAT-Enhancer-Binding Proteins / genetics
  • CCAAT-Enhancer-Binding Proteins / physiology*
  • Cell Line
  • Female
  • Gene Expression Regulation / immunology
  • Hormones, Ectopic / biosynthesis*
  • Hormones, Ectopic / genetics
  • Intercellular Signaling Peptides and Proteins
  • Interleukin-13 / physiology*
  • Interleukin-4 / physiology*
  • Lung / immunology
  • Lung / metabolism
  • Lung / pathology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Nerve Growth Factor
  • Promoter Regions, Genetic / immunology
  • Protein Biosynthesis*
  • Proteins / genetics
  • Rats
  • Resistin
  • STAT6 Transcription Factor
  • Th2 Cells / immunology*
  • Th2 Cells / metabolism
  • Trans-Activators / metabolism
  • Trans-Activators / physiology*
  • Up-Regulation / genetics
  • Up-Regulation / immunology

Substances

  • Antigens
  • CCAAT-Enhancer-Binding Proteins
  • Hormones, Ectopic
  • Intercellular Signaling Peptides and Proteins
  • Interleukin-13
  • Proteins
  • Resistin
  • Retn protein, mouse
  • Retn protein, rat
  • Retnla protein, mouse
  • Retnla protein, rat
  • Retnlb protein, mouse
  • STAT6 Transcription Factor
  • Stat6 protein, mouse
  • Trans-Activators
  • Interleukin-4
  • Nerve Growth Factor