Abstract
We have shown that extracellular calcium [Ca+2]e induces cyclooxygenase-2 (COX-2) expression and prostaglandin E2 (PGE2) production via an ERK signaling pathway in osteoblasts. In this study, we examined the roles of protein kinase C (PKC) and A (PKA) signaling pathways in the [Ca+2]e induction of COX-2 in primary calvarial osteoblasts from mice transgenic for −371bp of the COX-2 promoter fused to a luciferase reporter. Neither PKC specific inhibitors nor downregulation of the PKC pathway by phorbol myristate acetate (PMA) affected the [Ca+2]e stimulation of COX-2 mRNA or promoter activity. In contrast, PKA inhibitors, used at doses that inhibited forskolin-stimulated luciferase activity by 90%, reduced [Ca+2]e-stimulated COX-2 mRNA expression and promoter activity by 80–90%. [Ca+2]e also stimulated a 2- to 3-fold increase in cAMP production. Hence, the [Ca+2]e induction of COX-2 mRNA expression and promoter activity was independent of the PKC pathway and dependent on the PKA signaling pathway.
Published Version
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