Differential activation of signal transducer and activator of transcription 6 in B cells from allergic children and their non-allergic siblings

Clin Exp Allergy. 2004 Apr;34(4):576-82. doi: 10.1111/j.1365-2222.2004.1911.x.

Abstract

Background: The germline (GL) epsilon promoter is regulated by IL-4 and is essential for class switching to IgE. IL-4-induced gene expression is largely mediated through activation of latent transcription factor STAT6 (signal transducer and activator of transcription 6).

Objective: We investigated whether increased levels of IgE in allergic individuals may be associated with alteration in the level or activation of STAT6 and subsequent increase in GL epsilon promoter activity.

Methods: Electrophoretic mobility shift assay and Western blotting assays were used to investigate the level of expression and activation of STAT6 in Epstein-Barr virus (EBV)-transformed B cell lines from children with birch pollen allergy and their non-allergic siblings. The activity of the GL epsilon promoter was tested in a transient transfection assay.

Results: STAT6 was expressed at the same level in all B cell lines tested. In two out of five sibling pairs STAT6 was activated by IL-4 more efficiently in the allergic individuals but in the three other pairs the opposite was found. In transient transfections, no difference in IL-4-induced GL epsilon promoter function was detected, although basal promoter activity varied between allergic and healthy siblings in two out of five pairs.

Conclusions: We demonstrate for the first time that upon IL-4 signalling STAT6 transcription factor activation differs in B cells from different individuals. Although we did not find any association between STAT6 activation and allergy, we do not exclude a possibility that stronger activation of this transcription factor is associated with an expression of allergic phenotype.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • B-Lymphocytes / immunology*
  • Betula / immunology
  • Cell Transformation, Viral
  • Child
  • Child, Preschool
  • DNA-Binding Proteins / metabolism
  • Female
  • Herpesvirus 4, Human / immunology
  • Humans
  • Hypersensitivity / genetics
  • Hypersensitivity / immunology*
  • Immunoglobulin Class Switching / immunology
  • Immunoglobulin E / biosynthesis
  • Immunoglobulin epsilon-Chains / genetics
  • Immunoglobulin epsilon-Chains / immunology
  • Interleukin-4 / immunology
  • Male
  • Phosphorylation
  • Pollen / immunology
  • Promoter Regions, Genetic
  • STAT6 Transcription Factor
  • Trans-Activators / metabolism*
  • Transfection

Substances

  • DNA-Binding Proteins
  • Immunoglobulin epsilon-Chains
  • STAT6 Transcription Factor
  • STAT6 protein, human
  • Trans-Activators
  • Interleukin-4
  • Immunoglobulin E