Cronshaw Darran G, Kouroumalis Andreas, Parry Richard, Webb Adam, Brown Zarin, Ward Stephen G
Department of Pharmacy & Pharmacology, University of Bath, Claverton Down, Bath, Avon, UK BA2 7AY.
J Leukoc Biol. 2006 Jun;79(6):1369-80. doi: 10.1189/jlb.0106035. Epub 2006 Apr 13.
Macrophage-derived chemokine [CC chemokine ligand 22 (CCL22)] and thymus- and activation-regulated chemokine (CCL17) mediate cellular effects, principally by binding to their receptor CC chemokine receptor 4 (CCR4) and together, constitute a multifunctional chemokine/receptor system with homeostatic and inflammatory roles within the body. This study demonstrates that CCL22 and CCL17 stimulate pertussis toxin-sensitive elevation of intracellular calcium in the CEM leukemic T cell line and human peripheral blood-derived T helper type 2 (Th2) cells. Inhibition of phospholipase C (PLC) resulted in the abrogation of chemokine-mediated calcium mobilization. Chemokine-stimulated calcium responses were also abrogated completely by the inhibition of inositol 1,4,5-trisphosphate [Ins(1,4,5)P3] receptor-mediated calcium release. Chemotactic responses of CEM and human Th2 cells to CCL17 and CCL22 were similarly abrogated by inhibition of PLC and inhibition of novel, Ca2+-independent/diacylglycerol-dependent protein kinase C (PKC) isoforms. Inhibition of Ins(1,4,5)P3 receptor-mediated calcium release from intracellular stores had no effect on chemotactic responses to CCR4 ligands. Taken together, this study provides compelling evidence of an important role for PLC and diacylglycerol-dependent effector mechanisms (most likely involving novel PKC isoforms) in CCL17- and CCL22-stimulated, directional cell migration. In this regard, CCL22 stimulates phosphatidylinositol-3 kinase-independent phosphorylation of the novel delta isoform of PKC at threonine 505, situated within its activation loop--an event closely associated with increased catalytic activity.
巨噬细胞衍生趋化因子[CC趋化因子配体22(CCL22)]和胸腺与活化调节趋化因子(CCL17)主要通过与它们的受体CC趋化因子受体4(CCR4)结合来介导细胞效应,二者共同构成了一个多功能趋化因子/受体系统,在体内发挥稳态和炎症调节作用。本研究表明,CCL22和CCL17可刺激CEM白血病T细胞系和人外周血来源的2型辅助性T细胞(Th2细胞)内钙水平升高,且该升高对百日咳毒素敏感。磷脂酶C(PLC)的抑制导致趋化因子介导的钙动员作用消失。肌醇1,4,5-三磷酸[Ins(1,4,5)P3]受体介导的钙释放受到抑制后,趋化因子刺激的钙反应也完全消失。抑制PLC以及抑制新型的、不依赖Ca2+ /依赖二酰基甘油的蛋白激酶C(PKC)亚型,同样会消除CEM细胞和人Th2细胞对CCL17和CCL22的趋化反应。抑制Ins(1,4,5)P3受体介导的细胞内钙库钙释放,对CCR4配体的趋化反应没有影响。综上所述,本研究提供了有力证据,证明PLC和依赖二酰基甘油的效应机制(极有可能涉及新型PKC亚型)在CCL17和CCL22刺激的定向细胞迁移中发挥重要作用。在这方面,CCL22可刺激PKC新型δ亚型在其激活环内的苏氨酸505位点发生不依赖磷脂酰肌醇-3激酶的磷酸化,这一事件与催化活性增加密切相关。