## Abstract To study the physiological control of osteoclasts, the bone resorbing cells, we generated transgenic mice carrying the Cre recombinase gene driven by either the tartrateβresistant acid phosphatase (TRAP) or cathepsin K (Ctsk) promoters. TRAPβCre and CtskβCre transgenic mouse lines were
Targeted expression of Cre recombinase in macrophages and osteoclasts in transgenic mice
β Scribed by M. Ferron; J. Vacher
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 671 KB
- Volume
- 41
- Category
- Article
- ISSN
- 1526-954X
No coin nor oath required. For personal study only.
β¦ Synopsis
To develop specific conditional gene ablation in the hematopoietic myeloid-osteoclast lineage, transgenic mice expressing Cre recombinase under the control of the CD11b promotor were generated on the C57BL/6 background. The cellular specificity of Cre activity following recombination was quantified in the Z/EG reporter transgenic mice by FACS analysis with lineage-specific markers and EGFP coexpression. A high degree of recombination, as evidenced by EGFP-positive cells, was demonstrated in macrophages and granulocytes of bone marrow and spleen by the presence of double-positive cells CD11b/EGFP and Gr1/EGFP, respectively. Interestingly, the peritoneal macrophage population showed almost complete DNA recombination at large. Most important, mature osteoclast cells derived from the double transgenic bone marrow and spleen progenitors were EGFP-positive. Hence, these CD11b-Cre mice will provide a unique tool to unravel novel gene function and activities involved during osteoclast and macrophage differentiation and maturation processes.
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