Wu Meng-Huang, Hsu Wei-Bin, Chen Mei-Hsin, Shi Chung-Sheng
Department of Orthopaedics, School of Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan.
Department of Orthopedics, Taipei Medical University Hospital, Taipei 11031, Taiwan.
Biomedicines. 2022 Sep 21;10(10):2355. doi: 10.3390/biomedicines10102355.
Neddylation, or the covalent addition of NEDD8 to specific lysine residue of proteins, is a reversible posttranslational modification, which regulates numerous biological functions; however, its involvement and therapeutic significance in osteoporosis remains unknown. Our results revealed that during the soluble receptor activator of nuclear factor-κB ligand (sRANKL)-stimulated osteoclast differentiation, the neddylation and expression of UBA3, the NEDD8-activating enzyme (NAE) catalytic subunit, were dose- and time-dependently upregulated in RAW 264.7 macrophages. UBA3 knockdown for diminishing NAE activity or administering low doses of the NAE inhibitor MLN4924 significantly suppressed sRANKL-stimulated osteoclast differentiation and bone-resorbing activity in the macrophages by inhibiting sRANKL-stimulated neddylation and tumor necrosis factor receptor-associated factor 6 (TRAF6)-activated transforming growth factor-β-activated kinase 1 (TAK1) downstream signaling for diminishing nuclear factor-activated T cells c1 (NFATc1) expression. sRANKL enhanced the interaction of TRAF6 with the neddylated proteins and the polyubiquitination of TRAF6's lysine 63, which activated TAK1 downstream signaling; however, this process was inhibited by MLN4924. MLN4924 significantly reduced osteoporosis in an ovariectomy- and sRANKL-induced osteoporosis mouse model in vivo. Our novel finding was that NAE-mediated neddylation participates in RANKL-activated TRAF6-TAK1-NFATc1 signaling during osteoclast differentiation and osteoporosis, suggesting that neddylation may be a new target for treating osteoporosis.
NEDD8化,即NEDD8共价连接到蛋白质特定赖氨酸残基上,是一种可逆的翻译后修饰,可调节多种生物学功能;然而,其在骨质疏松症中的作用及治疗意义尚不清楚。我们的结果显示,在核因子κB受体活化因子配体(sRANKL)刺激破骨细胞分化过程中,RAW 264.7巨噬细胞中NEDD8活化酶(NAE)催化亚基UBA3的NEDD8化及表达呈剂量和时间依赖性上调。敲低UBA3以降低NAE活性或给予低剂量的NAE抑制剂MLN4924,可通过抑制sRANKL刺激的NEDD8化以及肿瘤坏死因子受体相关因子6(TRAF6)激活的转化生长因子-β激活激酶1(TAK1)下游信号传导,减少核因子活化T细胞c1(NFATc1)表达,从而显著抑制sRANKL刺激的巨噬细胞破骨细胞分化和骨吸收活性。sRANKL增强了TRAF6与NEDD8化蛋白的相互作用以及TRAF6赖氨酸63的多聚泛素化,激活了TAK1下游信号传导;然而,该过程被MLN4924抑制。在去卵巢和sRANKL诱导的骨质疏松症小鼠体内模型中,MLN4924显著减轻了骨质疏松症。我们的新发现是,NAE介导的NEDD8化在破骨细胞分化和骨质疏松症过程中参与RANKL激活的TRAF6-TAK1-NFATc1信号传导,提示NEDD8化可能是治疗骨质疏松症的新靶点。