Charreau B, Tesson L, Buscail J, Soulillou J P, Anegon I
INSERUM U437, Nantes, France.
Transgenic Res. 1996 Nov;5(6):443-50. doi: 10.1007/BF01980209.
The investigation of human complement (C) inhibitors with a view to overcoming C-mediated tissue injury stands to benefit from the production of anatomically suitable transgenic animals. In this study, we used the CMV-IE1 enhancer/promoter to control the expression in vivo in transgenic rats of the human terminal C protein inhibitor CD59. Five transgenic rats were identified, of which four possessed at least one complete copy of the transgene. The presence of human CD59 transcripts and protein was demonstrated in two transgenic rat lines. A widespread tissue distribution of cells expressing human CD59, similar in the two lines, was observed-principally in pancreas, brain, heart, kidney, intestine and striated muscle. Whereas expression in pancreas and brain was uniform, mosaicism of CD59 expression was observed in some tissues such as heart and kidney, a proportion of cells within the tissue not expressing the transgene. Immunohistological analysis revealed surface expression of human CD59 in a variety of cells, including fibroblasts, epithelial cells and muscle cells, but not in endothelial cells. In conclusion, this paper analyses at the cellular level human CD59 expression directed by the CMV promoter in transgenic rats, amd discusses how they could be used to investigate in vivo the role of C in a variety of pathologies.
为了克服补体(C)介导的组织损伤而对人类补体抑制剂展开的研究,有望受益于制作解剖结构合适的转基因动物。在本研究中,我们使用巨细胞病毒立即早期蛋白1(CMV-IE1)增强子/启动子来控制人类末端补体蛋白抑制剂CD59在转基因大鼠体内的表达。鉴定出了5只转基因大鼠,其中4只至少拥有一个完整的转基因拷贝。在两个转基因大鼠品系中证实了人类CD59转录本和蛋白的存在。观察到表达人类CD59的细胞在组织中广泛分布,这两个品系情况相似——主要存在于胰腺、脑、心脏、肾脏、肠道和横纹肌中。胰腺和脑中的表达是均匀的,而在心脏和肾脏等一些组织中观察到CD59表达存在镶嵌现象,即组织内一部分细胞不表达转基因。免疫组织学分析显示人类CD59在多种细胞表面表达,包括成纤维细胞、上皮细胞和肌肉细胞,但在内皮细胞中不表达。总之,本文在细胞水平分析了由CMV启动子指导的人类CD59在转基因大鼠中的表达,并讨论了如何利用它们在体内研究补体在多种病理状态中的作用。