RAC1/P38 MAPK signaling pathway controls β1 integrin-induced interleukin-8 production in human natural killer cells

被引:86
作者
Mainiero, F
Soriani, A
Strippoli, R
Jacobelli, J
Gismondi, A
Piccoli, M
Frati, L
Santoni, A
机构
[1] Univ Rome La Sapienza, Inst Pasteur, Fdn Cenci Bolognetti, Dept Expt Med & Pathol, I-00161 Rome, Italy
[2] Regina Elena Inst Canc Res, Lab Pathophysiol, I-00158 Rome, Italy
[3] Mediterranean Inst Neursci Neuromed, I-86077 Pozzilli, Italy
关键词
D O I
10.1016/S1074-7613(00)80154-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The MAP kinase (MAPK) p38 plays a key role in regulating inflammatory responses. Here, we demonstrate that beta 1 integrin ligation on human NK cells results in the activation of the p38 MAPK signaling pathway, which is required for integrin-triggered IL-8 production. In addition, we identified some of the upstream events accompanying the beta 1 integrin-mediated p38 MAPK activation, namely, the activation of the Rac guanine nucleotide exchange factor (GEF) p95 Vav, the small G protein Rac1, and the cytoplasmic kinases Pak1 and MKK3. Finally, we provide direct evidence that p95 Vav and Rac control the activation of p38 MAPK triggered by beta 1 integrins.
引用
收藏
页码:7 / 16
页数:10
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