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转人CD59基因小鼠对人补体介导的免疫反应的保护作用
引用本文:武玉东,刘秉乾,李胜芝,李光三. 转人CD59基因小鼠对人补体介导的免疫反应的保护作用[J]. 郑州大学学报(医学版), 2005, 40(3): 430-432
作者姓名:武玉东  刘秉乾  李胜芝  李光三
作者单位:郑州大学第一附属医院泌尿外科,郑州,450052;天津市泌尿外科研究所,天津,300211;中国科学院遗传与发育生物学研究所,北京,100080
基金项目:天津市科技发展计划基金资助项目043803411
摘    要:目的:探讨转基因小鼠血管内皮细胞特异性表达人CD59(hCD59)基因对人补体介导的免疫反应的保护作用。方法:通过显微注射方法建立转hCD59基因小鼠,采用PCR、Southernblot方法检测hCD59基因的整合,流式细胞仪检测hCD59蛋白的表达,人血清体外灌注转基因小鼠心脏、免疫组织化学染色补体C9及IgG评估排斥反应的情况。结果:转基因小鼠hCD59基因表达强度为人外周血白细胞的35%~120%,转基因小鼠体外灌注心脏存活时间明显延长(P<0.01),心脏补体C9沉积明显减少。结论:血管内皮细胞特异性表达hCD59可以减轻异种移植排斥反应,延长移植物的存活时间。

关 键 词:异种移植  排斥反应  CD59基因  小鼠  转基因动物
修稿时间:2004-12-28

Transgenic mice expressing recombinant human CD59 gene against human complement-mediated attack
Wu Yudong,LIU Bingqian,LI Shengzhi,LI Guangsan. Transgenic mice expressing recombinant human CD59 gene against human complement-mediated attack[J]. Journal of Zhengzhou University: Med Sci, 2005, 40(3): 430-432
Authors:Wu Yudong  LIU Bingqian  LI Shengzhi  LI Guangsan
Affiliation:WU Yudong 1),LIU Bingqian 2),LI Shengzhi 2),LI Guangsan 3) 1)Department of Urology,the Frist Affiliated Hospital,Zhengzhou University,Zhengzhou 450052 2)Tianjin Institute of Urological Surgery,Tianjin 300211 3)Institute of Heredity and Developmental Biology,Chinese Academy of Science,Beijing 100080
Abstract:Aim: To explore the role of expression of recombinant human CD59 (hCD59) gene in transgenic mice endothelial cells against human complement-mediated attack. Methods: Transgenic mice expressing hCD59 were generated by microinjection of a recombinant hCD59 gene under the control the human ICAM-2 promoter. The offspring were tested for transgene integration by using PCR and Southern blot, and for hCD59 expression on peripheral blood leukocytes (PBLs) by flow cytometry. Hearts from transgenic mices were perfused in vitro with human plasma. Immune rejection was evaluated by immunohistochemical analysis of hearts for C9 and IgG. Results: Expression levels of hCD59 ranged from 35% to 120% of that on human PBLs. Hearts perfused with human plasma showed longer survival time, and deposition of human C9 was greatly reduced in transgenic hearts. Conclusion: High-level vascular endothelial-specific expression of hCD59 could overcome hypercute rejection of xenotransplantation,and prolong xenograft survival.
Keywords:xenotransplantation  rejection  CD59 gene  mice  transgenic animal
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