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生成在肾脏集合管细胞中特异性表达 Cre 重组酶的 AQP2-Cre 转基因小型猪。

Generation of AQP2-Cre transgenic mini-pigs specifically expressing Cre recombinase in kidney collecting duct cells.

机构信息

College of Animal Science, Jilin University, 5333 Xi'an Road, Changchun, 130062, People's Republic of China.

出版信息

Transgenic Res. 2014 Apr;23(2):365-75. doi: 10.1007/s11248-013-9774-8. Epub 2013 Dec 5.

Abstract

The important differences in physiological parameters and anatomical characteristics of the kidney between humans and mice make it difficult to replicate the precise progression of human renal cystic diseases in gene modification mouse models. In contrast to mice, pigs are a better animal model of human diseases, as they are more similar in terms of organ size, structure, and physiological parameters. Here, we report the generation and initial examination of an AQP2-Cre transgenic (Tg) Chinese miniature (mini)-pig line that expresses Cre recombinase exclusively in kidney collecting duct cells. An 8-kb fragment of the mini-pig aquaporin 2 (AQP2) 5'-flanking region was utilized to direct Cre expression in Tg mini-pigs. Two Tg mini-pigs were generated by pig somatic cell nuclear transfer and both carried the entire coding sequence of Cre recombinase. RT-PCR and western blotting analysis revealed that Cre recombinase was uniquely expressed in the kidney, while immunohistochemical studies located its expression in kidney collecting duct cells. Furthermore, six integration sites and 12-14 copies of the Cre gene were detected in various tissues by high-efficiency thermal asymmetric interlaced PCR and absolute quantitative real-time PCR, respectively. Combined with previous studies of Cre recombinase activity, we believe that this AQP2-Cre Tg mini-pig line will be a useful tool to generate kidney collecting duct cell-specific gene knockout mini-pig models, thereby allowing the investigation of gene functions in kidney development and the mechanisms of human renal cystic disease.

摘要

人类和小鼠肾脏在生理参数和解剖特征方面存在重要差异,这使得在基因修饰小鼠模型中复制人类肾囊性疾病的精确进展变得困难。与小鼠相比,猪是更好的人类疾病动物模型,因为它们在器官大小、结构和生理参数方面更为相似。在这里,我们报告了一种 AQP2-Cre 转基因(Tg)中国迷你(mini)猪系的产生和初步检查,该猪系在肾脏集合管细胞中特异性表达 Cre 重组酶。利用迷你猪水通道蛋白 2(AQP2)的 8-kb 片段的 5'-侧翼区域来指导 Tg 迷你猪中 Cre 的表达。通过猪体细胞核转移生成了两只 Tg 迷你猪,它们都携带 Cre 重组酶的完整编码序列。RT-PCR 和 Western blot 分析显示,Cre 重组酶仅在肾脏中表达,而免疫组织化学研究将其表达定位在肾脏集合管细胞中。此外,通过高效热不对称交错 PCR 和绝对定量实时 PCR 分别在各种组织中检测到了 6 个整合位点和 12-14 个 Cre 基因拷贝。结合 Cre 重组酶活性的先前研究,我们相信这种 AQP2-Cre Tg 迷你猪系将成为生成肾脏集合管细胞特异性基因敲除迷你猪模型的有用工具,从而能够研究基因在肾脏发育和人类肾囊性疾病机制中的功能。

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