Jackson J K, Tudan C, Sahl B, Pelech S L, Burt H M
Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, Canada.
Immunology. 1997 Apr;90(4):502-10. doi: 10.1046/j.1365-2567.1997.d01-2178.x.
The activation of MAP kinase in human neutrophils stimulated by both uncoated and plasma-opsonized crystals of triclinic calcium pyrophosphate dihydrate (CPPD) was investigated. The effect of taxol on MAP kinase activation and on the responses of neutrophils stimulated by plasma-opsonized crystals was determined. MAP kinase activation was identified and quantified in Mono Q chromatography separated fractions of neutrophils that had been incubated with CPPD crystals by measuring [gamma-32P]adenosine triphosphate (ATP) phosphorylation of myelin basic protein and using immunoblotting techniques. Human neutrophils were incubated with taxol (0-50 microM), added to plasma-opsonized CPPD (50 mg/ml) and MAP kinase activation, chemiluminescence, superoxide anion generation, lysozyme and myeloperoxidase release were monitored. Both uncoated and plasma coated CPPD crystals induced a large increase in MAP kinase activity in neutrophils over control levels within 1 min of incubation. Pretreatment of neutrophils with taxol was able to suppress this activation of MAP kinase. Taxol produced a concentration-dependent inhibition of opsonized CPPD-induced neutrophil chemiluminescence, superoxide anion production and myeloperoxide release. Taxol at 28 microM also significantly inhibited chemiluminescence, superoxide anion production and myeloperoxidase release from neutrophils stimulated by opsonized zymosan. This is the first report of crystal-induced activation of MAP kinase in neutrophils. Microtubule-associated processes, such as signal transduction, secretion and phagocytosis are involved in particulate-induced neutrophil responses. We have suggested that the inhibitory effect of taxol observed in this work is due to its stabilizing effect on microtubules and disruption of MAP kinase activation associated with microtubules.
研究了由未包被和血浆调理的二水合焦磷酸钙(CPPD)三斜晶体刺激的人中性粒细胞中丝裂原活化蛋白激酶(MAP激酶)的激活情况。测定了紫杉醇对MAP激酶激活以及对血浆调理晶体刺激的中性粒细胞反应的影响。通过测量髓鞘碱性蛋白的[γ-32P]三磷酸腺苷(ATP)磷酸化并使用免疫印迹技术,在与CPPD晶体孵育的中性粒细胞经单Q色谱分离的组分中鉴定并定量MAP激酶激活。将人中性粒细胞与紫杉醇(0 - 50 microM)孵育,加入血浆调理的CPPD(50 mg/ml),并监测MAP激酶激活、化学发光、超氧阴离子生成、溶菌酶和髓过氧化物酶释放。未包被和血浆包被的CPPD晶体在孵育1分钟内均诱导中性粒细胞中MAP激酶活性比对照水平大幅增加。用紫杉醇预处理中性粒细胞能够抑制这种MAP激酶的激活。紫杉醇对调理后的CPPD诱导的中性粒细胞化学发光、超氧阴离子产生和髓过氧化物释放产生浓度依赖性抑制。28 microM的紫杉醇也显著抑制了调理后的酵母聚糖刺激的中性粒细胞的化学发光、超氧阴离子产生和髓过氧化物释放。这是关于晶体诱导中性粒细胞中MAP激酶激活的首次报道。微管相关过程,如信号转导、分泌和吞噬作用参与了颗粒诱导中性粒细胞反应。我们认为在这项工作中观察到的紫杉醇的抑制作用是由于其对微管的稳定作用以及对与微管相关的MAP激酶激活的破坏。