Interleukin-1β-induced interleukin-6 production in A549 cells is mediated by both phosphatidylinositol 3-kinase and interleukin-1 receptor-associated kinase-4

被引:23
|
作者
Eda, Hiroyuki [1 ]
Burnette, Barry L. [1 ]
Shimada, Hideaki [1 ]
Hope, Heidi R. [1 ]
Monahan, Joseph B. [1 ]
机构
[1] St Louis Labs Pfizer Inc, Discovery Biol, Global Res & Dev, Chesterfield, MO 63017 USA
关键词
interleukin-6 (IL-6); interleukin-1 receptor associated kinase-4 (IRAK4); phosphatidylinositol 3-kinase (PI3K); rheumatoid arthritis synovial fibroblast (RASF); signal transduction; small interfering RNA (siRNA); NF-KAPPA-B; ACTIVATION; PHOSPHORYLATION; REQUIRES; IRAK;
D O I
10.1042/CBI20100247
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The aim of this study is to investigate whether PI3K (phosphatidylinositol-3-kinase) is involved in IL-1 beta(interleukin-1 beta)-induced IL-6 production in A549 (human lung adenocarcinoma epithelial cell) and human RASF (rheumatoid arthritis synovial fibroblast). PI3K inhibitor, LY294002 significantly reduced IL-1 beta-induced IL-6 production in A549 cells but not in RASF, indicating that IL-1 beta-induced IL-6 production was partially mediated by PI3Kin A549 cells but not in RASF. siRNA (small interfering RNA) of IRAK4 (IL-1 receptor-associated kinase 4) treatment decreased IRAK4 mRNA level by up to 90% in A549 cells. In this condition, IL-1 beta-induced increase of IL-6 mRNA and protein level was decreased by up to 93% and 70%, respectively. Furthermore, the combination of IRAK4 siRNA and LY294002 treatment decreased protein induction level of IL-6 in A549 cells compared with that of IRAK4 siRNA or LY294002 alone. These results indicate that IL-1 beta-induced IL-6 production in A549 cells is mediated by both PI3K and IRAK4 and suggest that involvement of PI3K in the IL-1-induced IL-6 production is cell type specific.
引用
收藏
页码:355 / 358
页数:4
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