Prado Gregory N, Suetomi Katsutoshi, Shumate David, Maxwell Carrie, Ravindran Aishwarya, Rajarathnam Krishna, Navarro Javier
Department of Neuroscience and Cell Biology, Sealy Centers for Molecular Medicine and Structural Biology and Molecular Biophysics, University of Texas Medical Branch, Galveston, Texas 77555, USA.
Biochemistry. 2007 Aug 7;46(31):8961-8. doi: 10.1021/bi7004043. Epub 2007 Jul 13.
Chemokine IL-8 (CXCL8) binds to its cognate receptors CXCR1 and CXCR2 to induce inflammatory responses, wound healing, tumorogenesis, and neuronal survival. Here we identify the N-loop residues in IL-8 (H18 and F21) and the receptor N-termini as the major structural determinants regulating the rate of receptor internalization, which in turn controlled the activation profile of ERK1/2, a central component of the receptor/ERK signaling pathway that dictates signal specificity. Our data further support the idea that the chemokine receptor core acts as a plastic scaffold. Thus, the diversity and intensity of inflammatory and noninflammatory responses mediated by chemokine receptors appear to be primarily determined by the initial interaction between the receptor N-terminus and the N-loop of chemokines.
趋化因子白细胞介素-8(CXCL8)与其同源受体CXCR1和CXCR2结合,以诱导炎症反应、伤口愈合、肿瘤发生和神经元存活。在此,我们确定白细胞介素-8中的N环残基(H18和F21)以及受体N末端是调节受体内化速率的主要结构决定因素,而受体内化速率反过来又控制ERK1/2的激活模式,ERK1/2是决定信号特异性的受体/ERK信号通路的核心组成部分。我们的数据进一步支持趋化因子受体核心充当可塑性支架的观点。因此,趋化因子受体介导的炎症和非炎症反应的多样性和强度似乎主要由受体N末端与趋化因子N环之间的初始相互作用决定。