Differential regulation of syndecan expression by osteosarcoma cell lines in response to cytokines but not osteotropic hormones

Bone cells are regulated by interactions with both growth factors and compo nents of the extracellular matrix (ECM), Syndecans are cell-surface heparan sulfate proteoglycans known to play a role in cell adhesion and migration, and binding of growth factors. This study was performed to investigate the expression of syndecans by osteoblasts. Reverse transcription-linked polym erase chain reaction (RT-PCR) and Northern analysis detected syndecan trans cripts in the human osteosarcoma cell lines MG-63, TE-85, SaOS-2, and U2OS; human osteoblast-like cells; rat calvarial osteoblasts; and in human bone. Western blot analysis of proteoglycans from MG-63 and TE-85 cells detected multiple heparan sulfate proteoglycan core proteins consistent with syndec an expression, Regulation of syndecan-1, -2, and -4 expression was investig ated in TE-85, MG-63, and SaOS-2 cells, in response to interleukin (IL)-1 b eta, and IL-6, parathyroid hormone [PTH(1-34)], and 1,25(OH)(2)-vitamin D-3 . Northern analysis demonstrated that in the osteosarcoma cell lines there was no regulation of syndecan transcript levels in response to PTH(1-34) or 1,25(OH)(2)-vitamin D-3 for 24 or 48 h. In contrast, when MG-63 and SaOS-2 cells were incubated with IL-1 beta (0.01-10 ng/mL) and IL-6 (0.1-50 ng/mL ) there was a dose-dependent decrease in mRNA levels for syndecan-1 and 2 a t 24 and 48 h, but in response to IL-1 beta upregulation in the levels of s yndecan-4 transcripts, In addition, Northern analysis was performed on RNA isolated from neonatal rat calvarial osteoblasts cultured under conditions that promote osteogenesis for 0, 5, 13, 21, and 35 days. Syndecan-1 express ion was observed to decrease during the culture period, syndecan-2 transcri pt levels increased, and there appeared to be no overall change in syndecan -4 levels. Controlled expression of syndecans by cells of the osteoblast li neage may be important in the regulation of osteoblastic proliferation and differentiation. (Bone 24:571-578; 1999) (C) 1999 by Elsevier Science Inc. All rights reserved.