Development of a new canine osteosarcoma cell line

被引:8
|
作者
Seguin, B.
Zwerdling, T.
McCallan, J. L.
DeCock, H. E. V.
Dewe, L. L.
Naydan, D. K.
Young, A. E.
Bannasch, D. L.
Foreman, O.
Kent, M. S.
机构
[1] Univ Calif Davis, Sch Vet Med, Dept Surg & Radiol Sci, Davis, CA 95616 USA
[2] Univ Calif Davis, Sch Med, Dept Pediat, Davis, CA 95616 USA
[3] Univ Calif Davis, Sch Vet Med, Dept Pathol Microbiol & Immunol, Davis, CA 95616 USA
[4] Univ Calif Davis, Sch Vet Med, Vet Med Teaching Hosp, Pathol Serv, Davis, CA 95616 USA
[5] Univ Calif Davis, Sch Vet Med, Dept Populat Hlth & Reprod, Davis, CA 95616 USA
关键词
canine osteosarcoma; cell line; immunocytochemistry; immunohistochemistry; microsatellite DNA;
D O I
10.1111/j.1476-5829.2006.00112.x
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Establishing a canine osteosarcoma (OSA) cell line can be useful to develop in vivo and in vitro models of OSA. The goal of this study was to develop, characterize and authenticate a new canine OSA cell line and a clone. A cell line and a clone were developed with standard cell culture techniques from a naturally occurring OSA in a dog. The clonal cell line induced a tumour after injection in RAG 1-deficient mouse. Histology was consistent with OSA. The original tumour from the dog and the tumour induced in the mouse were both reactive with vimentin and osteonectin (ON). The parent cell line and clonal cell line were reactive with ON, osteocalcin and alkaline phosphatase. Loss of heterozygosity was found in the same three microsatellite markers in the parent and clonal cell lines, and the tumour tissue grown in the mouse.
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页码:232 / 240
页数:9
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