Molecular characterization of gene expression changes in ROS 17/2.8 cells cultured in diffusion chambers in vivo

• Published in: Calcified tissue international 1999-08, Vol.65 (2), p.133-138
• Main Authors: Onyia, J E, Hale, L V, Miles, R R, Cain, R L, Tu, Y, Hulman, J F, Hock, J M, Santerre, R F
• Format: Article
• Language: English
• Subjects: Animals; Biomarkers, Tumor - genetics; Blotting, Northern; Bone Neoplasms - chemistry; Bone Neoplasms - genetics; Bone Neoplasms - pathology; Cells, Cultured; Diffusion Chambers, Culture; DNA, Complementary - genetics; DNA, Neoplasm - analysis; Fibroblasts - chemistry; Fibroblasts - cytology; Gene Expression; In Situ Hybridization; Male; Osteosarcoma - chemistry; Osteosarcoma - genetics; Osteosarcoma - pathology; Rats; Rats, Sprague-Dawley; RNA, Messenger - metabolism
• ISSN: 0171-967X; 1432-0827
• DOI: 10.1007/s002239900671

Transplantation of diffusion chambers (DC) containing osteoblast-like cells to extraskeletal sites has been highly studied and proven to be a useful technique to investigate the process of osteoblast differentiation and bone formation. To investigate the molecular basis of osteogenesis in DC, we examined the temporal pattern of gene expression of the proliferation marker histone H4, immediate early response genes (IEGs), c-fos, c-jun, c-myc, osteoblast phenotype-associated genes, osteocalcin (OC), osteopontin (OP), type I collagen (COL1A1), alkaline phosphatase (ALP), parathyroid hormone receptor (PTHR) and matrix modifying enzyme, matrix metalloproteinase-9 (MMP-9). DC containing ROS 17/2.8 were implanted intraperitoneally into rat hosts and cultured in vivo for various times up to 56 days. Histological analysis of von Kossa stained sections of the DC contents showed a well-organized connective tissue and the production of mineralized matrices/nodules. In contrast, histological examination of DC containing Rat-2 fibroblast cells revealed the lack of an organized mineralized matrix. Molecular analysis of DC containing ROS 17/2.8 cells at 0, 3, 10, 28, and 56 days demonstrated a time-dependent decrease in DNA content associated with cell death. In the surviving cells, an increase in histone H4 mRNA (consistent with an increase in cell proliferation) was evident by 3-10 days and thereafter expression returned to control levels. In vitro, ROS 17/2.8 cells expressed detectable levels of c-fos, c-jun, c-myc, OC, OP, ALP, COL1A1, and PTHR but not MMP-9. In vivo, the expression of c-fos increased 2-fold in 3-28 days and by 56 days was 4-5 fold above control levels. In 3-10 days, c-jun expression increased 1.6-1.8-fold above control levels. In contrast, by day 28, c-jun expression decreased to control levels, but increased to 2.1-fold above control by 56 days. c-myc mRNA expression increased 3-fold within 3 days and then dropped to below control values by 10-56 days. After transplantation in vivo, the expression of OC and PTHR decreased to undetectable levels. Similarly, ALP mRNA decreased to