ScholarWorks@숙명여자대학교

초록

We investigated the effects of phosphodiesterase 3 (PDE3) and PDE4 inhibitors, which are cAMP degrading enzymes, on prostaglandin E-2 (PGE(2))-induced osteoclast formation. A PDE4 inhibitor decreased PGE(2)-induced osteoclast formation, whereas a PDE3 inhibitor did not, possibly due to the lack of PDE3 expression in RAW 264.7 cells. Cell cycle analysis revealed that the PDE4 inhibitor stimulated PGE(2)-induced p27(KIP1) expression, which leads to increased growth arrest at G(0)/G(1) phase. The PDE4 inhibitor increased cyclooxygenase 2 (COX-2) expression in the presence of PGE(2). COX-2 overexpression was associated with growth suppression via p27(KIP1) expression in RAW 264.7 cells. Taken together, our data demonstrate that the PDE4 inhibitor enhances PGE(2)-induced growth arrest of osteoclast precursors via COX-2-mediated p27(KIP1) expression, which in turn negatively regulates osteoclast formation.

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