Department of Histology and Oral Histology, Institute of Health Biosciences, The University of Tokushima Graduate School, Tokushima, Japan.
PLoS One. 2013 Sep 11;8(9):e72033. doi: 10.1371/journal.pone.0072033. eCollection 2013.
Diseases of bone loss are a major public health problem. Here, we report the novel therapeutic action of simvastatin in osteoclastogenesis and osteoprotection, demonstrated by the ability of simvastatin to suppress osteoclast formation in vitro and in vivo. We found that in vitro, IRF4 expression is upregulated during osteoclast differentiation induced by RANKL (receptor activator of nuclear factor-κB ligand), while simvastatin blocks RANKL-induced osteoclastogenesis and decreases expression of NFATc1 (nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 1), IRF4 and osteoclast markers. We also show that IRF4 acts in cooperation with NFATc2 and NF-κB on the promoter region of NFATc1 to accelerate its initial transcription during the early stage of osteoclastogenesis. Moreover, our study using IRF4 siRNA knockdown directly demonstrates the requirement for IRF4 in NFATc1 mRNA transcription and its necessity in RANKL-induced osteoclast differentiation. Our results suggest that the reduction in osteoclastogenesis is partly due to the inhibition of IRF4 production in RANKL-induced osteoclast differentiation. To investigate the in vivo effects of simvastatin in RANKL-treated mice, we examined the bone mineral density (BMD) of a mouse model of bone loss, and found that simvastatin significantly reduced bone loss by suppressing osteoclast numbers in vivo, even in the presence of high concentrations of RANKL. These results suggest that the depletion of osteoclasts is not due to the reduction in RANKL produced by osteoblasts in vivo. The results are consistent with the hypothesis that simvastatin blocks RANKL-induced IRF4 expression in osteoclastogenesis. We propose that the expression of IRF4 by osteoclasts could be a promising new therapeutic target in bone-loss diseases.
骨骼疾病是一个主要的公共健康问题。在这里,我们报告了辛伐他汀在破骨细胞生成和骨保护方面的新的治疗作用,这是通过辛伐他汀在体外和体内抑制破骨细胞形成来证明的。我们发现,在体外,IRF4 的表达在核因子-κB 配体(receptor activator of nuclear factor-κB ligand,RANKL)诱导的破骨细胞分化过程中上调,而辛伐他汀阻断 RANKL 诱导的破骨细胞生成,并降低 NFATc1(核因子活化 T 细胞的细胞质,钙调神经磷酸酶依赖 1)、IRF4 和破骨细胞标志物的表达。我们还表明,IRF4 在 NFATc1 启动子区域与 NFATc2 和 NF-κB 协同作用,以在破骨细胞生成的早期加速其初始转录。此外,我们使用 IRF4 siRNA 敲低的研究直接证明了 IRF4 在 NFATc1 mRNA 转录中的必要性及其在 RANKL 诱导的破骨细胞分化中的必要性。我们的结果表明,破骨细胞生成减少部分是由于 RANKL 诱导的破骨细胞分化中 IRF4 产生的抑制。为了研究辛伐他汀在 RANKL 处理的小鼠体内的作用,我们检查了一种骨丢失小鼠模型的骨密度(bone mineral density,BMD),发现辛伐他汀通过抑制体内破骨细胞数量显著减少骨丢失,即使在存在高浓度 RANKL 的情况下也是如此。这些结果表明,破骨细胞的耗竭不是由于体内成骨细胞产生的 RANKL 减少所致。这些结果与辛伐他汀阻断破骨细胞生成中 RANKL 诱导的 IRF4 表达的假设一致。我们提出,破骨细胞中 IRF4 的表达可能是骨丢失疾病的一个有前途的新治疗靶点。