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Transgenic mouse lines were generated that express the Cre recombinase under the control of the distal promoter of the mouse Lck gene. Cre recombination in four of these lines of transgenic mice was characterized at the single cell level using ROSA26-regulated loxP-Stop-loxP-betageo and loxP-Stop-loxP-YFP reporter mouse lines. Two of the lines showed T cell-restricted Cre recombination, whereas the other two also expressed Cre in B cells, NK cells, and monocytes. Cre recombination began at a late stage of T cell development (at or after up-regulation of the TCR during positive selection) in the two T cell-restricted lines. Lines of mice that express the Cre recombinase at late stages of thymocyte development are of value for determining the impact of mutations on T cell function in the absence of complicating effects on early thymocyte selection.
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Dong Ji Zhang
Qi Wang
Jie Wei
The Journal of Immunology
University of California, San Francisco
Technische Universität Dresden
Novartis (United States)
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Zhang et al. (Wed,) studied this question.
www.synapsesocial.com/papers/69fca8520b34e5e35ddd937b — DOI: https://doi.org/10.4049/jimmunol.174.11.6725