Department of Orthopaedics, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Key Laboratory of Musculoskeletal System Degeneration and Regeneration Translational Research of Zhejiang Province, Hangzhou, China.
J Bone Miner Res. 2019 May;34(5):911-922. doi: 10.1002/jbmr.3655. Epub 2019 Jan 7.
Pamapimod (PAM) is a novel selective p38 mitogen-activated protein (MAP) kinase inhibitor proved to be effective in rheumatoid arthritis in phase 2 clinical trial. However, its effect on osteoclast-associated osteoporosis and the underlying mechanisms remain unclear. In this study, we showed that PAM suppressed receptor activator of nuclear factor-κB ligand (RANKL)-induced osteoclast formation via inhibition of p38 phosphorylation and subsequent c-Fos and nuclear factor of activated T cells c1 (NFATc1) expression. In addition, the downregulated NFATc1 leads to reduced expression of its targeting gene disintegrin and metalloproteinase domain-containing protein 12 (ADAM12), which was further proven to be critical for osteoclastic bone resorption. Therefore, we treated ovariectomized (OVX) mice with PAM and revealed a protective effect of PAM on osteoporosis in vivo. In conclusion, our results demonstrated PAM can prevent OVX-induced bone loss through suppression of p38/NFATc1-induced osteoclast formation and NFATc1/ADAM12-associated bone resorption. © 2018 American Society for Bone and Mineral Research.
帕玛度胺(PAM)是一种新型的选择性 p38 丝裂原活化蛋白(MAP)激酶抑制剂,在 2 期临床试验中已被证明对类风湿关节炎有效。然而,其对破骨细胞相关骨质疏松症的影响及其潜在机制仍不清楚。在这项研究中,我们表明 PAM 通过抑制 p38 磷酸化以及随后的 c-Fos 和活化 T 细胞核因子 c1(NFATc1)表达,抑制核因子κB 受体激活剂配体(RANKL)诱导的破骨细胞形成。此外,下调的 NFATc1 导致其靶向基因解整合素和金属蛋白酶域蛋白 12(ADAM12)的表达减少,这被进一步证明对破骨细胞的骨吸收至关重要。因此,我们用 PAM 治疗去卵巢(OVX)小鼠,并在体内揭示了 PAM 对骨质疏松症的保护作用。总之,我们的结果表明,PAM 可以通过抑制 p38/NFATc1 诱导的破骨细胞形成和 NFATc1/ADAM12 相关的骨吸收来预防 OVX 诱导的骨丢失。