磷酸化
p38丝裂原活化蛋白激酶
MAPK/ERK通路
基因
细胞生物学
化学
生物
遗传学
作者
Kittipong Maneechotesuwan,Yao Xin,Kazuhiro Ito,Elen Jazrawi,Kang-Yun Lee,Omar S. Usmani,Peter J. Barnes,Ian M. Adcock
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2007-02-15
卷期号:178 (4): 2491-2498
被引量:159
标识
DOI:10.4049/jimmunol.178.4.2491
摘要
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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