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Regulation of Th2 cytokine genes by p38 MAPK-mediated phosphorylation of GATA-3

  • Kittipong Maneechotesuwan
  • , Yao Xin
  • , Kazuhiro Ito
  • , Elen Jazrawi
  • , Kang Yun Lee
  • , Omar S. Usmani
  • , Peter J. Barnes*
  • , Ian M. Adcock
  • *Corresponding author for this work
  • Imperial College London
  • Mahidol University

Research output: Contribution to journalJournal Article peer-review

146 Scopus citations

Abstract

GATA-3 plays a critical role in allergic diseases by regulating the release of cytokines from Th2 lymphocytes. However, the molecular mechanisms involved in the regulation of GATA-3 in human T lymphocytes are not yet understood. Using small interfering RNA to knock down GATA-3, we have demonstrated its critical role in regulating IL-4, IL-5, and IL-13 release from a human T cell line. Specific stimulation of T lymphocytes by costimulation of CD3 and CD28 to mimic activation by APCs induces translocation of GATA-3 from the cytoplasm to the nucleus, with binding to the promoter region of Th2 cytokine genes, as determined by chromatin immunoprecipitation. GATA-3 nuclear translocation is dependent on its phosphorylation on serine residues by p38 MAPK, which facilitates interaction with the nuclear transporter protein importin-α. This provides a means whereby allergen exposure leads to the expression of Th2 cytokines, and this novel mechanism may provide new approaches to treating allergic diseases.

Original languageEnglish
Pages (from-to)2491-2498
Number of pages8
JournalJournal of Immunology
Volume178
Issue number4
DOIs
StatePublished - 15 02 2007
Externally publishedYes

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