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Regulation of Th2 Cytokine Genes by p38 MAPK-Mediated Phosphorylation of GATA-3
Author(s) -
Kittipong Maneechotesuwan,
Yao Xin,
Kazuhiro Ito,
Elen Jazrawi,
Kang-Yun Lee,
Omar S. Usmani,
Peter J. Barnes,
Ian M. Adcock
Publication year - 2007
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.178.4.2491
Subject(s) - phosphorylation , p38 mitogen activated protein kinases , mapk/erk pathway , gene , microbiology and biotechnology , chemistry , biology , genetics
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-alpha. 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.

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