Rincón Mercedes, Davis Roger J
Immunology Program, Department of Medicine, University of Vermont, Burlington, VT 05405, USA.
Immunol Rev. 2009 Mar;228(1):212-24. doi: 10.1111/j.1600-065X.2008.00744.x.
Activation of immune cells to mediate an immune response is often triggered by potential 'danger' or 'stress' stimuli that the organism receives. Within the mitogen-activated protein kinases (MAPKs) family, the stress-activated protein kinase (SAPK) group was defined as group of kinases that activated by stimuli that cause cell stress. In the immune cells, SAPKs are activated by antigen receptors (B- or T-cell receptors), Toll-like receptors, cytokine receptors, and physical-chemical changes in the environment among other stimuli. The SAPKs are established to be important mediators of intracellular signaling during adaptive and innate immune responses. Here we summarize what is currently known about the role of two sub-groups of SAPKs - c-Jun NH(2)-terminal kinase and p38 MAPK-in the function of specific components of the immune system and the overall contribution to the immune response.
免疫细胞的激活以介导免疫反应通常由机体接收到的潜在“危险”或“应激”刺激触发。在丝裂原活化蛋白激酶(MAPK)家族中,应激激活蛋白激酶(SAPK)组被定义为由引起细胞应激的刺激所激活的激酶组。在免疫细胞中,SAPK由抗原受体(B细胞或T细胞受体)、Toll样受体、细胞因子受体以及环境中的物理化学变化等其他刺激激活。SAPK被确定为适应性和先天性免疫反应期间细胞内信号传导的重要介质。在这里,我们总结了目前已知的关于SAPK的两个亚组——c-Jun氨基末端激酶和p38 MAPK——在免疫系统特定成分功能中的作用以及对免疫反应的总体贡献。