TY - JOUR
T1 - Regulation of Th2 cytokine genes by p38 MAPK-mediated phosphorylation of GATA-3
AU - Maneechotesuwan, Kittipong
AU - Xin, Yao
AU - Ito, Kazuhiro
AU - Jazrawi, Elen
AU - Lee, Kang Yun
AU - Usmani, Omar S.
AU - Barnes, Peter J.
AU - Adcock, Ian M.
PY - 2007/2/15
Y1 - 2007/2/15
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=33846935457&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.178.4.2491
DO - 10.4049/jimmunol.178.4.2491
M3 - 文章
C2 - 17277157
AN - SCOPUS:33846935457
SN - 0022-1767
VL - 178
SP - 2491
EP - 2498
JO - Journal of Immunology
JF - Journal of Immunology
IS - 4
ER -