Inhibitory effects of mevastatin and a geranylgeranyl transferase I inhibitor (GGTI-2166) on mononuclear osteoclast formation induced by receptor activator of NF脙脙脙脙B ligand (RANKL) or tumor necro

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• 作者：Woo ; Je-Tae ; Nakagawa ; Hiroshi ; Krecic ; Annette M. ; Nagai ; Kazuo ; Hamilton ; Andrew D. ; Sebti ; Said M. ; et. al.
• 关键词：pOC ; preosteoclast ; RANKL ; receptor activator of NF脙脙脙脙B ligand ; M-CSF ; macrophage colony-stimulating factor ; GGTI ; geranylgeranyl transferase inhibitor ; GGOH ; geranylgeraniol ; FTI ; farnesyl transferase inhibitor ; TRAP ; tartrate-resistant acid phospha
• 刊名：Biochemical Pharmacology
• 出版年：2005
• 期刊代码：2_00062952
• 类别：pha
• 出版时间：January 1, 2005
• 卷：69
• 期：1
• 页码：87-95
• 文件大小：472 K

摘要

We have previously reported that the statin mevastatin (compactin) reversibly inhibits the fusion of TRAP-positive mononuclear preosteoclasts (pOCs) into multinucleated osteoclasts and disrupts the actin ring in mature osteoclasts through the inhibition of protein prenylation. Protein geranylgeranylation, specifically, is known to be required for pOC fusion and for the function and survival of mature osteoclasts. However, it has not been determined whether protein geranylgeranylation is involved in early differentiation of osteoclasts (pOC formation). The current study shows that statins and the geranylgeranyl transferase I inhibitor GGTI-2166 inhibit the pOC formation induced by RANKL or TNF-α in cultures of both mouse marrow-derived macrophage-colony-stimulating factor (M-CSF) dependent monocytes (MD cells) and the mouse monocyte cell line RAW 264.7 (RAW cells). Mevastatin, 0.1–0.6 μM, inhibited the formation of pOCs induced by receptor activator of nuclear factor-κB ligand (RANKL) or tumor necrosis factor (TNF-α) in both cell cultures. The inhibitory effects of mevastatin were overcome by the addition of mevalonate, farnesyl pyrophosphate or geranylgeranyl pyrophosphate. GGTI-2166 inhibited TRAP activity induced by RANKL or TNF-α in both cell cultures and prevented the incorporation of [³H]all-trans geranylgeraniol into prenylated proteins in RAW cells. However, the farnesyl transferase inhibitor FTI-2153 did not inhibit TRAP activity although FTI prevented the incorporation of [¹⁴C]mevalonate into farnesylated proteins in RAW cells. Clostridium difficile cytotoxin B (toxin B) inhibited pOC formation induced by RANKL or TNF-α in both cell cultures. The inhibitory effects of statins and GGTI-2166 on pOC formation may result from the inhibition of the geranylgeranylation of G-proteins, such as Rho or Rac, suggesting that the geranylgeranylation of these proteins is involved in the early differentiation of progenitor cells into pOCs.