Institute of Biochemistry and Molecular Cell Biology, RWTH Aachen University, Pauwelsstrasse 30, Aachen, Germany.
Cell Signal. 2011 Jan;23(1):135-44. doi: 10.1016/j.cellsig.2010.08.013. Epub 2010 Aug 31.
c-Jun N-terminal kinase (JNK) is a member of the mitogen-activated protein kinase (MAPK) family and controls essential processes such as inflammation, cell differentiation, and apoptosis. JNK signalling is triggered by extracellular signals such as cytokines and environmental stresses. Macrophage migration inhibitory factor (MIF) is a pleiotropic pro-inflammatory cytokine with chemokine-like functions in leukocyte recruitment and atherosclerosis. MIF promotes MAPK signalling through ERK1/2, while it can either activate or inhibit JNK phosphorylation, depending on the cell type and underlying stimulation context. MIF activities are mediated by non-cognate interactions with the CXC chemokine receptors CXCR2 and CXCR4 or by ligation of CD74, which is the cell surface expressed form of the class II invariant chain. ERK1/2 signalling stimulated by MIF is dependent on CD74, but the receptor pathway involved in MIF activation of the JNK pathway is unknown. Here we comprehensively characterize the stimulatory effect of MIF on the canonical JNK/c-Jun/AP-1 pathway in fibroblasts and T cell lines and identify the upstream signalling components. Physiological concentrations of recombinant MIF triggered the phosphorylation of JNK and c-Jun and rapidly activated AP-1. In T cells, MIF-mediated activation of the JNK pathway led to upregulated gene expression of the inflammatory chemokine CXCL8. Activation of JNK signalling by MIF involved the upstream kinases PI3K and SRC and was found to be dependent on CXCR4 and CD74. Together, these data show that the CXCR4/CD74/SRC/PI3K axis mediates a rapid and transient activation of the JNK pathway as triggered by the inflammatory cytokine MIF in T cells and fibroblasts.
c-Jun N-末端激酶(JNK)是丝裂原活化蛋白激酶(MAPK)家族的成员,控制着炎症、细胞分化和细胞凋亡等基本过程。JNK 信号转导由细胞因子和环境应激等细胞外信号触发。巨噬细胞移动抑制因子(MIF)是一种多效性前炎症细胞因子,具有趋化因子样功能,可招募白细胞并促进动脉粥样硬化。MIF 通过 ERK1/2 促进 MAPK 信号转导,而其对 JNK 磷酸化的作用既可激活,也可抑制,这取决于细胞类型和潜在的刺激背景。MIF 通过与 CXC 趋化因子受体 CXCR2 和 CXCR4 的非同源相互作用或与 CD74 的结合来发挥作用,CD74 是 II 类不变链的细胞表面表达形式。MIF 刺激的 ERK1/2 信号转导依赖于 CD74,但 MIF 激活 JNK 途径的受体途径尚不清楚。在这里,我们全面描述了 MIF 对成纤维细胞和 T 细胞系中经典 JNK/c-Jun/AP-1 途径的刺激作用,并确定了上游信号成分。生理浓度的重组 MIF 触发 JNK 和 c-Jun 的磷酸化,并迅速激活 AP-1。在 T 细胞中,MIF 介导的 JNK 途径激活导致炎症趋化因子 CXCL8 的基因表达上调。MIF 激活 JNK 信号转导涉及上游激酶 PI3K 和 SRC,并且发现该过程依赖于 CXCR4 和 CD74。总之,这些数据表明,在 T 细胞和成纤维细胞中,由炎症细胞因子 MIF 触发的 CXCR4/CD74/SRC/PI3K 轴介导了 JNK 途径的快速和短暂激活。