摘要
目的为证明旁路活化补体降低吞噬细胞功能,了解宿主抗感染能力下降的条件与机制。方法分离人中性粒细胞(PMN)和大鼠枯否细胞(KC);PMN和KC培养单层加上酵母多糖活化人血清(ZAHS);观测吞噬细胞胞内杀菌力(ICBA)、超氧阴离子(O-2)、酸性磷酸酶(ACP)指标动态水平;以抗人C3C5血清(AHC3C5S)中和阻断ZAHS进行反证。结果007~009mlZAHS处理组,KC胞内O-2水平在3小时前高于对照组值,然后逐渐下降。003~005mlZAHS6小时略有下降。ICBA其动态变化与O-2的相似,但003~005ml4小时后略有下降。ACP水平只降无升,随ZAHS用量增加,下降幅度越低,以上各指标至6小时降至最低。011mlZAHS处理组4小时后约85%~90%KC破裂脱落。ZAHS作用PMN的指标动态基本类似KC的动态,只是PMN指标在2小时之前升高,然后逐渐下降,以005~009mlZAHS对PMN指标影响最大。阻断组O-2、ACP、ICBA在6小时测定值显著高于ZAHS处理组,但仍低于正常对照。结论ZAHS使吞噬细胞功能下降与C3C5碎片作用有关,在大中剂量作用时间较长的条件?
Objective To verify host antiinfect capacity induced by bypass activated complement. Methods A monolayer culture of human PMNs and rats kupffer cells (KCs) were added with zymosan activated human serum (ZAHS) and 3 parameters were measured. ZAHS had been neutralized in tube with antiserum against human C 3 and C 5. Results In 0.07 0.09 ml ZAHS and 1 3h, intracellular bactericidal activity (ICBA) showed a peak but significant top value at 2nd hour. The value dropped markedly with time and significantly in 4 6 h. Superoxide ions (O - 2) dynamics was similar to ICBA. Acid phosphatase (ACP) curve distinguished from the former′s with monotonous decrease (1 6 h) and more deep. With 0.11 ml ZAHS after 4 h, about 80% of KCs were fallen off. Three parameters of PMNs were decreased and reached the lowest point in the 6 th hour after the adding 0.05~ 0.09 ml of ZAHS. After blocking test with antihuman C 3 and C 5 serum, the values of ICBA, O - 2 and ACP surpassed those in the experimental group. Conclusion The possible machanism of the origination of the harmful effects of ZAHS is suggested. Before KCs and PMNs undertake phagocytosis, they release the bactericidal and inflamagenic (O - 2 and ACP) so the intracellular bactericidal activity of KCs and PMNs are decreased. The accumulation of KCs and PMNs in tissues can demage themselves and the adjacent tissues barrier, which will lead to the occurrence of infection.
出处
《中华医学杂志》
CAS
CSCD
北大核心
1999年第4期250-252,共3页
National Medical Journal of China
关键词
补体
枯否细胞
抗感染
创伤
感染
Complement Kupffer cells Anti infective agents