Division of Bio-Imaging, Proteo-Science Center (PROS), Ehime University, Ehime, 791-0295, Japan.
Tokyo Metropolitan Police Hospital, 164-8541, Tokyo, Japan.
Nat Commun. 2017 Dec 20;8(1):2226. doi: 10.1038/s41467-017-02368-5.
C-C chemokine receptor 5 (CCR5) is a co-receptor of HIV. Epidemiological findings suggest that the functional loss of CCR5 is correlated with a lower incidence of bone-destructive diseases as well as of HIV transmission. However, it is not clear whether CCR5 is involved in regulation of the function of bone cells, in addition to that of immune cells. Here we show that blockade of CCR5 using specific antibodies impairs human osteoclast function in vitro. Ccr5-deficient (Ccr5 ) mice presented with dysfunctional osteoclasts and were resistant to osteoporosis induced by receptor activator of nuclear factor kappa-B ligand (RANKL), which triggers osteoporosis independently of inflammatory and immunomodulatory pathways. Furthermore, Ccr5 deficiency impairs the cellular locomotion and bone-resorption activity of osteoclasts, which is associated with the disarrangement of podosomes and adhesion complex molecules including Pyk2. Overall, the data provides evidence that CCR5 has an essential role in bone-destructive conditions through the functional regulation of osteoclasts.
C-C 趋化因子受体 5(CCR5)是 HIV 的共受体。流行病学研究结果表明,CCR5 的功能丧失与较低的破骨疾病发生率以及 HIV 传播率相关。然而,目前尚不清楚 CCR5 是否除了参与免疫细胞的功能调节外,还参与骨细胞的功能调节。在这里,我们发现使用特异性抗体阻断 CCR5 会损害体外人类破骨细胞的功能。缺乏 Ccr5(Ccr5 )的小鼠表现出破骨细胞功能障碍,并且对核因子 kappa-B 配体(RANKL)诱导的骨质疏松症具有抗性,RANKL 独立于炎症和免疫调节途径引发骨质疏松症。此外,Ccr5 缺乏会损害破骨细胞的细胞迁移和骨吸收活性,这与破骨细胞的足突和粘附复合物分子(包括 Pyk2)的排列紊乱有关。总体而言,这些数据表明 CCR5 通过对破骨细胞的功能调节在破骨疾病中发挥重要作用。