Marked Osteoblastopenia and Reduced Bone Formation in a Model of Multiple Myeloma Bone Disease in Severe Combined Immunodeficiency Mice

• Published in: Journal of bone and mineral research Vol. 14; no. 2; pp. 256 - 263
• Main Authors: Hjorth‐Hansen, Henrik, Seifert, Mark F., Börset, Magne, Aarset, Harald, Östlie, Agnes, Sundan, Anders, Waage, Anders
• Format: Journal Article
• Language: English
• Published: Washington, DC John Wiley and Sons and The American Society for Bone and Mineral Research (ASBMR) 01.02.1999; American Society for Bone and Mineral Research
• Subjects: AIDS/HIV; Animals; Biological and medical sciences; Bone Diseases, Metabolic - etiology; Bone Diseases, Metabolic - metabolism; Bone Diseases, Metabolic - pathology; Calcium - blood; Disease Models, Animal; Experimental and animal immunopathology. Animal models; Female; Hepatocyte Growth Factor - biosynthesis; Humans; Immunopathology; Medical sciences; Mice; Mice, SCID; Multiple Myeloma - complications; Multiple Myeloma - metabolism; Multiple Myeloma - pathology; Neoplasm Transplantation; Osteoblasts - pathology; Osteogenesis; Transplantation, Heterologous; Tumor Cells, Cultured; Immunopathology; Animal model; Rodentia; Diseases of the osteoarticular system; Malignant hemopathy; Bone disease; Myeloma; Immune deficiency; Osteoarticular system; Vertebrata; Mammalia; Cell line; Immunoglobulinopathy; Mouse; Lymphoproliferative syndrome; Animal; Osteoblast; Bone; Formation
• ISSN: 0884-0431; 1523-4681
• DOI: 10.1359/jbmr.1999.14.2.256

We report on an in vivo model of human myeloma producing bone disease in irradiated severe combined immunodeficiency disease mice using the human myeloma cell line JJN‐3 and its subline JJN‐3 T1. The cell lines are not Epstein‐Barr virus transformed and produce large amounts of hepatocyte growth factor (HGF). Mice had radiological signs of osteolysis and mild hypercalcemia. Xenografted cells were predominantly found in bone marrow and brown adipose tissue, but also in meninges and liver. Take was documented by histopathological examination, immunophenotyping of cultured bone marrow, and radiography. HGF was detected in serum and bone marrow plasma. Disease generally occurred within 45 days of intravenous inoculation and was signaled by paraparesis or signs of intracranial neoplasia. More than 90% of the mice had take of xenografts. The subline JJN‐3 T1 gave more reproducible bone marrow take than the native cell line. Bone histomorphometric examination revealed a 99% reduction in osteoblast counts and a 33% reduction in osteoclast counts in areas of tumor growth. Bone formation rates were reduced by 53%. The results suggest that osteoblastopenia and reduced bone formation is of importance for the occurrence of osteolytic lesions in this model.