Comparative analysis of the efficiency and specificity of myeloid-Cre deleting strains using ROSA-EYFP reporter mice

被引:372
作者
Abram, Clare L. [1 ,2 ]
Roberge, Gray L. [1 ,2 ]
Hu, Yongmei [1 ,2 ]
Lowell, Clifford A. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Program Immunol, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
Cre-recombinase; Floxed; Dendritic cell; Macrophage; Neutrophil; DENDRITIC CELLS; T-CELLS; MEDIATED RECOMBINATION; MAMMALIAN GENOMES; TRANSGENIC MICE; MAST-CELL; EXPRESSION; MACROPHAGES; DEFICIENCY; ACTIVATION;
D O I
10.1016/j.jim.2014.05.009
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Since the first example of conditional gene targeting in mice in 1994, the use of Cre recombinase and loxP flanked sequences has become an invaluable technique to generate tissue and temporal specific gene knockouts. The number of mouse strains expressing foxed-gene sequences, and tissue-specific or temporal-specific Cre-recombinase that have been reported in the literature has grown exponentially. However, increased use of this technology has highlighted several problems that can impact the interpretation of any phenotype observed in these mouse models. In particular, accurate knowledge of the specificity of Cre expression in each strain is critical in order to make conclusions about the role of specific cell types in the phenotypes observed. Cre-mediated deletion specificity and efficiency have been described in many different ways in the literature, making direct comparisons between these Cre strains impossible. Here we report crossing thirteen different myeloid-Cre mouse strains to ROSA-EYFP reporter mice and assaying YFP expression in a variety of naive unstimulated hematopoietic cells, in parallel. By focusing on myeloid subsets, we directly compare the relative efficiency and specificity of myeloid deletion in these strains under steady-state conditions. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:89 / 100
页数:12
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