The Interaction between GATA Proteins and Activator Protein-1 Promotes the Transcription ofIL-13in Mast Cells
Author(s) -
Akio Masuda,
Yasunobu Yoshikai,
Hiroaki Kume,
Tetsuya Matsuguchi
Publication year - 2004
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.173.9.5564
Subject(s) - transactivation , gata2 , transcription factor , transcription (linguistics) , microbiology and biotechnology , transfection , biology , promoter , mast cell , activator (genetics) , interleukin 13 , gene , gene expression , interleukin 4 , immunology , cytokine , genetics , linguistics , philosophy
IL-13 is considered to be a key modulator in the pathogenesis of Th2-induced allergic inflammation, although little is known about the regulation of IL-13 transcription in mast cells. In T cells, involvement of GATA-3 in cell type-specific expression of the IL-13 gene has been reported. However, the mechanisms that induce rapid transactivation of the IL-13 gene in response to various types of stimulation have hitherto remained unknown. In this report, we describe our investigation of the promoter region necessary for IL-13 transcription; we have found that both AP-1 and GATA proteins are indispensable for IL-13 transcription in mouse mast cells. In our investigation, we focused on the functional interaction between GATA and AP-1 in the IL-13 promoter context. Transfection experiments have revealed that GATA-1 and GATA-2 proteins are able to associate with AP-1 proteins. We have also shown that overexpression of GATA-1 induced excess AP-1 binding to the IL-13 promoter as well as a significant increase in IL-13 production in mast cells. The results of the present study have shown that direct interaction between AP-1 and GATA proteins plays an important role in IL-13 transcription in mast cells.
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