Effect of Combined Action of Extracellular ATP and Elevated Calcium on Osteogenic Differentiation of Primary Cultures From Rat Calvaria

ABSTRACT The in vitro osteogenic differentiation has been intensively studied. However, it is not yet clear precisely how osteogenesis can be optimized. Changes in extracellular Ca2+ concentration ([Ca2+]e), as well as modulation of purinergic receptors play an important role in the regulation of osteoblasts differentiation and bone formation. In this study, we investigated the effects of a combined treatment of ATPγ‐S and high [Ca2+]e (5.35 mM) on osteogenic differentiation and function of primary cell cultures from rat calvaria. Our results indicate that ATPγ‐S stimulates cell transition from the G0 to S phase of cell cycle, involving the PI3K signaling pathway. Treatment with 10 or 100 µM ATPγ‐S and [Ca2+]e (ATP‐[Ca2+]e) for 48 h increases cell number significantly above the control. ATPγ‐S treatment in osteogenic medium containing [Ca2+]e stimulates the gene expression of BMP‐4, BMP‐5, and OPN at 16, 48, and 72 h, respectively, above control. In same conditions, treatment for 6 days with 10 µM UTP or 100 µM UDP significantly increased the ALP activity respect to control. Cells grown in osteogenic medium showed a statistically significant increase in calcium deposits at 15 and 18 days, for 10 µM ATPγ‐S treatment, and at 18 and 22 days, for [Ca2+]e treatment, respect to control but ATP‐[Ca2+]e treatment shown a significant greater mineralization at 15 days respect to ATPγ‐S, and at 18 days respect to both agonists. In conclusion, we demonstrated that an osteogenic medium containing 10 µM ATPγ‐S and 5.35 mM [Ca2+]e enhance osteogenesis and mineralization by rat primary calvarial cells cultures. J. Cell. Biochem. 117: 2658–2668, 2016. © 2016 Wiley Periodicals, Inc. ATPγ‐S stimulates cell transition from G0 to S phase of cell cycle, involving the PI3K signaling pathway in primary cell cultures from rat calvaria. Combined treatment of 10 or 100 μM ATPγ‐S and 5.35 mM Ca2+ (ATP‐[Ca2+]e) stimulates proliferation of rat calvarial cell. Cell ATP‐[Ca2+]e treatment in osteogenic medium stimulates the gene expression of BMP‐4, BMP‐5, and OPN. ATP‐[Ca2+]e treatment shown a significantly greater mineralization at 15 days respect to ATPγ‐S, and at 18 days respect to both agonists.