摘要
目的:证明一定条件下,旁路活化补体可使KC吞噬杀菌功能失常。方法:观测定量培养的KC在ZAHS作用下吞噬杀菌及分泌杀菌致炎物质功能的动态水平;观察大鼠肠系膜注射ZAHS后肝组织的病理改变;以抗人C3、C5血清中和的ZAHS进行反证。结果:①ZAHS处理组,KC的PI和ICBA以及胞内O-2水平先升后降,胞内ACP水平只降无升;ICBA与O-2和ACP的水平均显著相关;各指标至6h降至最低;②阻断组O-2、ACP、ICBA在6h水平保持在正常对照组的97%、83%和79%,显著高于ZAHS处理组;③肠系膜静脉注射ZAHS12h后,大鼠肝组织轻度变性,部分KC线粒体受损,与KC相邻肝细胞出现凋亡改变,阻断组肝组织无明显病变。结论:ZAHS中过量的C3、C5碎片持续作用能使KC吞噬杀菌功能下降,对肝组织结构亦有一定间接破坏作用。
Objective: To determine whether bypass activated complement can directly influence intracellular bactericidal activity (ICBA) of Kupffer cells (KCs). Methods: ① Cultured KCs were challenged to different doses of ZAHS at different time phases and then 4 parameters were measured. ② In vivo, the rats were challenged to ZAHS injection through mesenteric vein. The liver was sampled and examined under LM and EM respectively 12 h later. ③ The same procedures were repeated except that ZAHS had been neutralized by the serum against C3 and C5. Results: ① Phagocytic index (PI), ICBA and intracellular superoxide ions of ZAHS treated KCs rose significantly and then fell. Acid phosphatase (ACP) decreased monotonously decreased. ICBA was significantly correlated to both intracellular superoxide ions and ACP. ② After the 12th injection of ZAHS, the pathological changes in rat livers included albuminous degeneration of most hepatocytes, injured mitochondria of some KCs and apoptosis of few hepatocytes adjacent to KCs. ③ Block test showed that the anti serum treated KCs held 79% ICBA, 83% ACP and 97% intracellular superoxide ions respecting to the normal. No evident pathological changes in the livers of the challenged rats were seen. Conclusion: The fragments of C3 and C5 in ZAHS can directly impair phagocytic and bactericidal function of KCs and indirectly injure the structure of the liver. The mechanism of this might be the great release of bactericidal and inflammatogenic intracellular superoxide ions and ACP.
出处
《第三军医大学学报》
CAS
CSCD
北大核心
1999年第2期90-92,共3页
Journal of Third Military Medical University
关键词
补体
枯否细胞
胞内杀菌力
旁路活化补体
complement
Kupffer cell
superoxide ion
intracellular bactericidal activity
acid phosphatase