体液免疫反应对异种灌注大鼠肝脏非实质细胞的影响。

T. Uesugi, I. Ikai, S. Satoh, T. Yagi, A. Kanazawa, O. Takeyama, R. Nishitai, H. Okabe, N. Katsura, H. Terajima, R. Takahashi, Y. Yamaoka
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引用次数: 1

摘要

背景:研究异种体液免疫反应对异种灌注大鼠肝脏非实质细胞(NPCs)的影响。方法取离体大鼠肝脏经门静脉灌注240 min,灌注液由新鲜大鼠血(1组)、新鲜人血(2组)和含有5 μ g/mL可溶性补体受体1型的新鲜人血(3组)组成。结果2组观察到人IgM和C(5b-9)补体沉积,3组仅检测到人IgM沉积。第2组门静脉压力在前10 min急剧升高。各组肌酸激酶BB成分逐渐升高,随后丙氨酸转氨酶升高,且第2组两项参数均显著高于第1和第3组。2组在10min后出现外周静脉血小板血栓和门静脉周围出血,240min后出现中心静脉周围大量坏死;在第1组和第3组没有观察到这些变化。2组肿瘤坏死因子α和α干扰素的产生及细胞间粘附分子1 (ICAM-1)的表达低于1、3组。2组24min后中心静脉周围出现ICAM-1和肿瘤坏死因子α染色阴性区,与坏死区一致。结论在异种灌注大鼠肝脏中,体液介质首先引起微循环紊乱,引起中心周围区域长时间缺血,导致大面积坏死。鼻咽癌坏死可能是导致异种灌注肝细胞因子和粘附分子产生减少的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of humoral immunoreaction on hepatic nonparenchymal cells in ex situ xenoperfused rat livers.
BACKGROUND The influence of xenogeneic humoral immunoreaction on hepatic nonparenchymal cells (NPCs) was evaluated ex situ in xenoperfused rat livers. METHODS Isolated rat livers were perfused via the portal vein (PV) for 240 min. The perfusates consisted of fresh rat blood (group 1), fresh human blood (group 2), and fresh human blood containing 5 microg/mL soluble complement receptor type 1 (Group 3). RESULTS Deposition of human IgM and C(5b-9) complement was observed in group 2, although only human IgM deposition was detected in group 3. Portal vein pressure in group 2 rose drastically during the first 10 min. Creatine kinase BB component gradually increased in all groups, followed by an elevation in alanine aminotransferase and both parameters were significantly higher in group 2 than in groups 1 and 3. In group 2, platelet thrombi in the peripheral PVs and periportal hemorrhage were observed after 10 min, and massive necrosis around the central veins after 240 min; these changes were not observed in group 1 or 3. Production of tumor necrosis factor alpha and alpha interferon and expression of intercellular adhesion molecule 1 (ICAM-1) were lower in group 2 than in groups 1 and 3. In group 2, there were negative areas for ICAM-1 and tumor necrosis factor alpha staining around the central veins after 240 min, which were consistent with necrotic areas. CONCLUSIONS In xenoperfused rat livers, humoral mediators initially caused the disturbance of microcirculation, which would induce long ischemia in the pericentral areas, resulting in massive necrosis. NPC necrosis may be responsible for less production of cytokines and adhesion molecules in the xenoperfused livers.
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