Schmid E, Warner R L, Crouch L D, Friedl H P, Till G O, Hugli T E, Ward P A
Department of Pathology, University of Michigan Medical School Ann Arbor 48109, USA.
Inflammation. 1997 Jun;21(3):325-33. doi: 10.1023/a:1027302017117.
Using ELISA analysis, rat C5a was stimulated in serum from rats undergoing systemic activation of complement after intravenous infusion of purified cobra venom factor (CVF). Biological (neutrophil chemotactic) activity was also assessed. Serum levels of C5a were directly proportional to the amount of CVF infused. C5a and neutrophil chemotactic activity, peaked by 5 min, then plateaued. In vitro addition of anti-C5a to serum samples of CVF-infused rats totally abolished chemotactic activity, indicating that all biological activity could be ascribed to C5a. Blood neutrophils obtained from CVF-infused animals showed a significant upregulation of CD11b, the increase being reduced (38%) in animals pretreated with anti-C5a. These findings indicate that infusion of CVF into rats produces generation of C5a, all chemotactic activity in serum being related to C5a. The in vivo generation of C5a is, at least inpart, responsible for upregulation of CD11b on blood neutrophils.
采用酶联免疫吸附分析(ELISA),在静脉注射纯化眼镜蛇毒因子(CVF)后,对经历补体系统激活的大鼠血清中的大鼠C5a进行刺激。还评估了生物(中性粒细胞趋化)活性。血清C5a水平与注入的CVF量成正比。C5a和中性粒细胞趋化活性在5分钟时达到峰值,然后趋于平稳。向注入CVF的大鼠血清样本中体外添加抗C5a完全消除了趋化活性,表明所有生物活性都可归因于C5a。从注入CVF的动物获得的血液中性粒细胞显示CD11b显著上调,在用抗C5a预处理的动物中,这种增加减少了(38%)。这些发现表明,向大鼠注入CVF会产生C5a,血清中的所有趋化活性都与C5a有关。C5a的体内产生至少部分负责血液中性粒细胞上CD11b的上调。