Integrin-mediated Ras-extracellular regulated kinase (ERK) signaling regulates interferon γ production in human natural killer cells

被引:57
作者
Mainiero, F
Gismondi, A
Soriani, A
Cippitelli, M
Palmieri, G
Jacobelli, J
Piccoli, M
Frati, L
Santoni, A
机构
[1] Univ Rome La Sapienza, Dept Expt Med & Pathol, Ist Pasteur, Fdn Cenci Bolognetti, I-00161 Rome, Italy
[2] Ist Nazl Studio & Cura Tumori, Biotechnol Sect, I-16100 Genoa, Italy
[3] Mediterranean Inst Neurosci Neuromed, I-86170 Pozzilli, Italy
[4] Regina Elena Canc Inst, Lab Pathophysiol, I-00100 Rome, Italy
关键词
natural killer cells; integrins; Ras mitogen-activated protein kinase pathway; interferon gamma;
D O I
10.1084/jem.188.7.1267
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent evidence indicates that integrin engagement results in the activation of biochemical signaling events important for regulating different cell functions, such as migration, adhesion, proliferation, differentiation, apoptosis, and specific gene expression. Here, we report that beta 1 integrin ligation on human natural killer (NK) cells results in the activation of Ras/mitogen-activated protein kinase pathways. Formation of She-growth factor receptor-bound protein 2 (Grb2) and Shc-proline-rich tyrosine kinase 2-Grb2 complexes are the receptor-proximal events accompanying the beta 1 integrin-mediated Ras activation. In addition, we demonstrate that ligation of beta 1 integrins results in the stimulation of interferon gamma (IFN-gamma) production, which is under the control of extracellular signal-regulated kinase 2 activation. Overall, our data indicate that beta 1 integrins, by delivering signals capable of triggering IFN-gamma production, may function as NK-activating receptors.
引用
收藏
页码:1267 / 1275
页数:9
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