Establishment and Characterization of a Cell Line, MCO-Y4, Derived from Canine Mammary Gland Osteosarcoma

Journal of Veterinary Medical Science

Nguyen Thi LAN³  Tosiharu HAYASHI²  Kazuyuki UCHIDA¹  Ryoji YAMAGUCHI¹  Atsushi KAWABATA³  Susumu TATEYAMA¹  Kaori YAMAMOTO¹ 

[1] Department of Veterinary Pathology, Faculty of Agriculture, University of Miyazaki;Department of Veterinary Pathology, Faculty of Agriculture, Yamaguchi University;Departments of Pathogenetic and Preventive Veterinary Science, The United Graduate School of Veterinary Science, Yamaguchi University

关键词: bone morphogenetic protein;    canine mammary gland;    cell line;    noggin;    osteosarcoma;   

DOI  :  10.1292/jvms.68.1047

学科分类：兽医学

来源: Japanese Society of Veterinary Science

【 摘 要 】

References(42)Cited-By(1)A cell line, MCO-Y4, was established from a mammary gland osteosarcoma of a 16-year-old female mongrel dog. Histopathologically the tumor was composed of osteoblastic cells with an osteoid meshwork and chondroid matrix. The mean doubling time of the cells at the 93rd passage was 32.39 ± 4.66 hr. Immunohistochemically, the osteoblastic and chondroblastic cells were positive for bone morphogenetic protein (BMP)-2/4 and BMP receptor (BMPR) II. The cultured cells were spindle in shape during the growth and the confluent phases. No tumor matrix was detected in the culture dish by alcian blue staining or von-Kossa silver impregnation. MCO-Y4 cells on the chamber slides showed intense immunoreactivity for BMP-2/4 and BMPR II. Noggin, an antagonist for BMP-2/4, showed the growth inhibition on MCO-Y4 cells. In addition, fibronectin might be potential for stimulating growth of MCO-Y4 cells. When transplanted into severe combined immunodeficiency mice, the cells formed tumors consisting of solid proliferation of osteoblastic and fibroblastic cells with woven-bone trabeculae. These tumor cells were intensely positive for BMP-2/4 and BMPR II. Our results suggested that the cell line might be useful for studying the role of BMPs in canine osteosarcoma and the mechanism of ossification.

【 授权许可】

Unknown