Regulation of the immune response by stress-activated protein kinases

Authors


Mercedes Rincón
Immunology Program, Department of Medicine
Given Medical Building
University of Vermont
Burlington, VT 05405, USA
Tel.: +1 802 656 0937
Fax: +1 802 656 3854
e-mail: mrincon@uvm.edu

Abstract

Summary:  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 NH2-terminal kinase and p38 MAPK-in the function of specific components of the immune system and the overall contribution to the immune response.

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