Transgenic mice that express Cre recombinase in osteoclasts


Autoria(s): Chiu, W. S. M.; McManus, J. F.; Notini, A. J.; Cassady, A. I.; Zajac, J. D.; Davey, R. A.
Data(s)

01/07/2004

Resumo

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.

Identificador

http://espace.library.uq.edu.au/view/UQ:74034

Idioma(s)

eng

Publicador

John Wiley & Sons, Inc.

Palavras-Chave #Developmental Biology #Genetics & Heredity #Osteoclast #Cre Recombinase #Transgenic Mouse #Bone Metabolism #Resistant Acid-phosphatase #Gene-expression #Cathepsin K #Differentiation #Cells #Promoter #Lacz #Dna #C1 #270201 Gene Expression #780000 - Non-Oriented Research
Tipo

Journal Article