4.7 Article

Generation of T-cell receptor retrogenic mice

Journal

NATURE PROTOCOLS
Volume 1, Issue 1, Pages 406-417

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nprot.2006.61

Keywords

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Funding

  1. NCI NIH HHS [CA-21765] Funding Source: Medline
  2. NIAID NIH HHS [AI52199, AI39480] Funding Source: Medline
  3. NATIONAL CANCER INSTITUTE [P30CA021765] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R56AI052199, R21AI052199, R01AI052199, R29AI039480, R01AI039480] Funding Source: NIH RePORTER

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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.

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