Transgenic mice that express Cre recombinase in osteoclasts

被引:74
作者
Chiu, WSM
McManus, JF
Notini, AJ
Cassady, AI
Zajac, JD
Davey, RA [1 ]
机构
[1] Univ Melbourne, Dept Med, Austin Hlth, Heidelberg, Vic, Australia
[2] Univ Queensland, Inst Mol Biosci, St Lucia, Qld 4067, Australia
[3] Univ Queensland, Dept Biochem & Mol Biol, St Lucia, Qld 4067, Australia
关键词
osteoclast; Cre recombinase; transgenic mouse; bone metabolism;
D O I
10.1002/gene.20041
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
To study the physiological control of osteoclasts, the bone resorbing cells, we generated transgenic mice carrying the Cre recombinase gene driven by either the tartrate-resistant acid phosphatase (TRAP) or cathepsin K (Ctsk) promoters. TRAP-Cre and Ctsk-Cre transgenic mouse lines were characterized by breeding with LacZ ROSA 26 (R26R) reporter mice and immunohistochemistry for Cre recombinase. The Cre transgene was functional in all lines, with Cre-mediated recombination occurring primarily in the long bones, vertebrae, ribs, and calvaria. Histological analyses of the bones demonstrated that functional Cre protein was present in 1) osteoclasts (Ctsk-Cre); 2) osteoclasts, columnar proliferating, and hypertrophic chondrocytes (TRAP-Cre line 4); and 3) round proliferating chondrocytes (TRAP-Cre line 3). In conclusion, we generated transgenic mouse lines that will enable the deletion of floxed target genes in osteoclasts, which will be valuable tools for studying the regulation of osteoclast function. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:178 / 185
页数:8
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