Larsen G L, Presley D M, Graves J P, Giclas P C
Department of Pediatrics, National Jewish Center for Immunology and Respiratory Medicine, Denver, CO 80206.
Pediatr Pulmonol. 1991;11(4):302-9. doi: 10.1002/ppul.1950110406.
Our earlier investigations indicated that systemic complement activation with iv cobra venom factor (CVF) or infused zymosan-activated rabbit plasma or rabbit C5a does not significantly increase bronchoalveolar lavage albumin in rabbits (Am Rev Respir Dis 1982; 125:335-340); but that complement activation due to CVF combined with a brief episode of hypoxia increases lavage albumin and is associated with the presence of neutrophils for its expression (J Clin Invest 1985; 75:902-910). In order to determine if intravenous CVF and hypoxia cause similar alterations in mice, and to investigate the time course of the response as well as the importance of C5 fragments to the process, we challenged the B10.D2/nSn strain of C5 sufficient mice (C5+) and the congenic B10.D2/oSn strain of C5 deficient mice (C5-) with intravenous CVF, 15 min of 12% oxygen, or CVF followed by hypoxia. Neither C5+ nor C5- mice had significant increases in lavage protein after either CVF or hypoxia. However, the combined insults significantly increased lavage protein in C5+ but not C5- mice; polyacrylamide gel electrophoresis showed increased amounts of proteins of low and high molecular weights in lavage fluid from the C5+ strain. While the time course of abnormalities in mice was different from that in rabbits, both meclofenamate pretreatment and neutrophil depletion attenuated the increases in lavage protein after the combined insults in both animal species. Infusion of prostaglandin E2 (PGE2) with CVF in the C5+ mice also led to significant increases in lavage protein. We conclude that in mice, intravenous complement activation, as an isolated event, does not cause a significant increase in lavage protein.(ABSTRACT TRUNCATED AT 250 WORDS)
我们早期的研究表明,静脉注射眼镜蛇毒因子(CVF)、输注酵母聚糖激活的兔血浆或兔C5a进行全身补体激活,并不会显著增加兔支气管肺泡灌洗白蛋白(《美国呼吸与危重症医学杂志》1982年;125:335 - 340);但CVF引起的补体激活与短暂缺氧发作相结合会增加灌洗白蛋白,并与中性粒细胞的存在有关,以促进其表达(《临床研究杂志》1985年;75:902 - 910)。为了确定静脉注射CVF和缺氧是否会在小鼠中引起类似的改变,并研究反应的时间进程以及C5片段对该过程的重要性,我们用静脉注射CVF、15分钟12%氧气或CVF后再缺氧的方法,对C5充足的B10.D2/nSn品系小鼠(C5 +)和C5缺陷的同基因B10.D2/oSn品系小鼠(C5 -)进行了挑战。无论是C5 +还是C5 -小鼠,在注射CVF或缺氧后灌洗蛋白均无显著增加。然而,联合损伤显著增加了C5 +小鼠而非C5 -小鼠的灌洗蛋白;聚丙烯酰胺凝胶电泳显示,C5 +品系灌洗液中低分子量和高分子量蛋白质的含量增加。虽然小鼠异常的时间进程与兔子不同,但甲氯芬那酸预处理和中性粒细胞耗竭均减弱了两种动物在联合损伤后灌洗蛋白的增加。在C5 +小鼠中,将前列腺素E2(PGE2)与CVF一起输注也导致灌洗蛋白显著增加。我们得出结论,在小鼠中,静脉补体激活作为一个独立事件,不会导致灌洗蛋白显著增加。(摘要截短于250字)