Department of Physiology and Pathology, Araraquara School of Dentistry, University Estadual Paulista-UNESP, Araraquara, Brazil.
Immunol Invest. 2013;42(7):555-622. doi: 10.3109/08820139.2013.822766.
Chronic inflammatory processes close to bone often lead to loss of bone in diseases such as rheumatoid arthritis, periodontitis, loosened joint prosthesis and tooth implants. This is mainly due to local formation of bone resorbing osteoclasts which degrade bone without any subsequent coupling to new bone formation. Crucial for osteoclastogenesis is stimulation of mononuclear osteoclast progenitors by macrophage colony-stimulating factor (M-CSF) and receptor activator of nuclear factor-κB ligand (RANKL) which induces their differentiation along the osteoclastic lineage and the fusion to mature, multinucleated osteoclasts. M-CSF and RANKL are produced by osteoblasts/osteocytes and by synovial and periodontal fibroblasts and the expression is regulated by pro- and anti-inflammatory cytokines. These cytokines also regulate osteoclastic differentiation by direct effects on the progenitor cells. In the present overview, we introduce the basic concepts of osteoclast progenitor cell differentiation and summarize the current knowledge on cytokines stimulating and inhibiting osteoclastogenesis by direct and indirect mechanisms.
慢性炎症过程靠近骨骼往往导致骨丢失在疾病如类风湿关节炎、牙周炎、松动的关节假体和牙种植体。这主要是由于局部形成的骨吸收破骨细胞降解骨没有任何随后的耦合到新骨形成。关键的破骨细胞生成刺激单核细胞破骨细胞前体由巨噬细胞集落刺激因子(M-CSF)和核因子-κB 配体受体激活剂(RANKL)诱导它们沿着破骨细胞谱系分化和融合成熟,多核破骨细胞。M-CSF 和 RANKL 是由成骨细胞/成骨细胞和滑膜和牙周成纤维细胞产生的,其表达受前炎症和抗炎细胞因子调节。这些细胞因子也通过直接作用于祖细胞来调节破骨细胞分化。在本综述中,我们介绍了破骨细胞前体细胞分化的基本概念,并总结了目前关于通过直接和间接机制刺激和抑制破骨细胞生成的细胞因子的知识。