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T细胞受体逆转录基因小鼠的产生。

Generation of T-cell receptor retrogenic mice.

作者信息

Holst Jeff, Szymczak-Workman Andrea L, Vignali Kate M, Burton Amanda R, Workman Creg J, Vignali Dario A A

机构信息

Department of Immunology, St Jude Children's Research Hospital, 332 North Lauderdale, Memphis, Tennessee 38105, USA.

出版信息

Nat Protoc. 2006;1(1):406-17. doi: 10.1038/nprot.2006.61.

Abstract

T-cell receptor (TCR) transgenic (Tg) mice have revolutionized our understanding of many aspects of T-cell biology. Whereas they provide an almost unlimited source of T cells with a single specificity, breeding them onto different backgrounds and/or new knockout/knock-in mouse models is often time-consuming (6 months to several years), which can make the process costly and can significantly delay research. This protocol describes a new method for expressing defined TCR-alpha and TCR-beta proteins from a single 2A peptide-linked multicistronic retroviral vector in mice, using retrovirus-mediated stem cell gene transfer. We refer to these as 'retrogenic' (Rg) mice ('retro' from retrovirus and 'genic' from Tg) to avoid confusion with traditional transgenic mice. We have successfully used this approach to express over 50 different TCRs on several different mouse backgrounds in as little as 6 weeks.

摘要

T细胞受体(TCR)转基因(Tg)小鼠彻底改变了我们对T细胞生物学诸多方面的理解。尽管它们提供了几乎无限的单一特异性T细胞来源,但将它们培育到不同背景和/或新的基因敲除/基因敲入小鼠模型上通常很耗时(6个月到数年),这可能使过程成本高昂,并可能显著延迟研究。本方案描述了一种利用逆转录病毒介导的干细胞基因转移,在小鼠中从单个2A肽连接的多顺反子逆转录病毒载体表达特定TCR-α和TCR-β蛋白的新方法。我们将这些小鼠称为“逆转基因”(Rg)小鼠(“retro”来自逆转录病毒,“genic”来自转基因),以避免与传统转基因小鼠混淆。我们已成功使用这种方法,在短短6周内在几种不同的小鼠背景上表达了50多种不同的TCR。

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