Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 101, Issue 14, Pages 5140-5145Publisher
NATL ACAD SCIENCES
DOI: 10.1073/pnas.0306141101
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We investigated the direct effects of changes in free ionized extracellular calcium concentrations ([Ca2+](o)) on osteoblast function and the involvement of the calcium-sensing receptor (CaR) in mediating these responses. CaR mRNA and protein were detected in osteoblast models, freshly isolated fetal rat calvarial cells and murine clonal osteoblastic 2T3 cells, and in freshly frozen, undecalcified preparations of human mandible and rat femur. In fetal rat calvarial cells, elevating [Ca2+](o) and treatment with gadolinium, a nonpermeant CaR agonist, resulted in phosphorylation of the extracellular signal-regulated kinases 1 and 2, Akt, and glycogen-synthase kinase 3beta, consistent with signals of cell survival and proliferation. In agreement, cell number was increased under these conditions. Expression of the osteoblast differentiation markers core binding factor all, osteocalcin, osteopontin, and collagen 1 mRNAs was increased by high [Ca2+](o), as was mineralized nodule formation. Alkaline phosphatase activity was maximal for [Ca2+](o) between 1.2 and 1.8 mM. inhibition of CaR by NIPS 89636 blocked responses to the CaR agonists. In conclusion, we show that small deviations of [Ca2+](o) from physiological values have a profound impact on bone cell fate, by means of the CaR and independently of systemic calciotropic peptides.
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