Arthritis and Tissue Degeneration Program, The David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, 10021, NY, USA.
Department of Medicine, Weill Cornell Medical College, New York, 10065, NY, USA.
Nat Commun. 2018 Oct 5;9(1):4108. doi: 10.1038/s41467-018-06446-0.
Targeting microRNAs recently shows significant therapeutic promise; however, such progress is underdeveloped in treatment of skeletal diseases with osteolysis, such as osteoporosis and rheumatoid arthritis (RA). Here, we identified miR-182 as a key osteoclastogenic regulator in bone homeostasis and diseases. Myeloid-specific deletion of miR-182 protects mice against excessive osteoclastogenesis and bone resorption in disease models of ovariectomy-induced osteoporosis and inflammatory arthritis. Pharmacological treatment of these diseases with miR-182 inhibitors completely suppresses pathologic bone erosion. Mechanistically, we identify protein kinase double-stranded RNA-dependent (PKR) as a new and essential miR-182 target that is a novel inhibitor of osteoclastogenesis via regulation of the endogenous interferon (IFN)-β-mediated autocrine feedback loop. The expression levels of miR-182, PKR, and IFN-β are altered in RA and are significantly correlated with the osteoclastogenic capacity of RA monocytes. Our findings reveal a previously unrecognized regulatory network mediated by miR-182-PKR-IFN-β axis in osteoclastogenesis, and highlight the therapeutic implications of miR-182 inhibition in osteoprotection.
靶向 microRNAs 最近显示出显著的治疗潜力;然而,在治疗溶骨性骨骼疾病(如骨质疏松症和类风湿关节炎 (RA))方面,这种进展还不够发达。在这里,我们确定 miR-182 是骨稳态和疾病中关键的破骨细胞生成调节剂。髓系特异性敲除 miR-182 可保护小鼠免受卵巢切除诱导的骨质疏松症和炎症性关节炎疾病模型中过度的破骨细胞生成和骨吸收。用 miR-182 抑制剂对这些疾病进行药物治疗可完全抑制病理性骨侵蚀。从机制上讲,我们确定蛋白激酶双链 RNA 依赖性 (PKR) 是一个新的和必需的 miR-182 靶点,通过调节内源性干扰素 (IFN)-β 介导的自分泌反馈环,是破骨细胞生成的新型抑制剂。miR-182、PKR 和 IFN-β 的表达水平在 RA 中发生改变,并且与 RA 单核细胞的破骨细胞生成能力显著相关。我们的发现揭示了破骨细胞生成中由 miR-182-PKR-IFN-β 轴介导的先前未被认识的调节网络,并强调了抑制 miR-182 在骨保护中的治疗意义。