Normal matrix mineralization induced by strontium ranelate in MC3T3-E1 osteogenic cells

• Published in: Metabolism, clinical and experimental clinical and experimental, 2004-04, Vol.53 (4), p.532-537
• Main Authors: Barbara, A, Delannoy, P, Denis, B.G, Marie, P.J
• Format: Article
• Language: English
• Subjects: Alkaline Phosphatase - metabolism; Animals; Biological and medical sciences; Calcification, Physiologic - drug effects; Calcification, Physiologic - physiology; Calcitriol - analogs & derivatives; Calcitriol - pharmacology; Calcium - metabolism; Cell Line; Collagen - biosynthesis; Errors of metabolism; Extracellular Matrix - drug effects; Extracellular Matrix - metabolism; Extracellular Matrix - physiology; Lipids (lysosomal enzyme disorders, storage diseases); Magnesium - metabolism; Medical sciences; Metabolic diseases; Mice; Organometallic Compounds - metabolism; Organometallic Compounds - pharmacology; Osteoblasts - cytology; Osteoblasts - drug effects; Osteoblasts - metabolism; Osteogenesis - drug effects; Osteogenesis - physiology; Strontium - metabolism; Thiophenes - metabolism; Thiophenes - pharmacology
• ISSN: 0026-0495; 1532-8600
• DOI: 10.1016/j.metabol.2003.10.022

There is growing evidence that strontium ranelate (SR; S12911-2, PROTELOS; Institut de Recherches Internationales Servier, Courbevoie, France), a compound containing 2 atoms of stable strontium (Sr), influences bone cells and bone metabolism in vitro and in vivo. We previously reported that SR increases bone mass in rats and mice by stimulating bone formation and inhibiting bone resorption. We also showed that short-term treatment with SR enhances osteoblastic cell recruitment and function in short-term rat calvaria cultures. Because Sr incorporates into the bone matrix, it was of interest to determine whether SR may affect matrix mineralization in long-term culture. To this goal, osteogenic mouse calvaria-derived MC3T3-E1 osteoblastic cells were cultured for up to 14 days in the presence of ascorbic acid and phosphate to induce matrix formation and mineralization. Matrix formation was determined by incorporation of tritiated proline during collagen synthesis. Matrix mineralization was quantified by measuring the number and surface of mineralized nodules using a digital image analyzer. In this model, 1,25(OH)2 vitamin D (1 nmol/L) used as internal control, increased alkaline phosphatase (ALP) activity, an early osteoblast marker, on days 4, 10, and 14 of culture. Treatment with SR (1 mmol/L Sr 2+) increased ALP activity at days 4 and 14 of culture. SR also increased collagen synthesis at days 4 and 10 of culture. In contrast, 1,25(OH)2 vitamin D (1 nmol/L) inhibited collagen synthesis at 4 to 14 days of culture. Long-term treatment with SR (0.1 to 1 mmol/L Sr 2+) dose dependently increased Sr concentration into the calcified nodules, but did not alter matrix mineralization in long-term culture, as shown by the ratio of the surface of mineralized nodules to the number of mineralized nodules on day 14 of culture. These results show that long-term treatment with SR increases collagenous matrix formation by MC3T3-E1 osteoblasts without inducing deleterious effect on matrix mineralization.