Department of Orthopaedic Surgery and Cell Biology & Physiology, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Bone and Mineral Division, Department of Medicine, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Sci Rep. 2017 Oct 3;7(1):12600. doi: 10.1038/s41598-017-12707-7.
NF-κB signaling is essential for osteoclast differentiation and skeletal homeostasis. We have reported recently that NUMB-like (NUMBL) protein modulates osteoclastogenesis by down regulating NF-κB activation. Herein, we decipher the mechanism underlying this phenomenon. We found that whereas NUMBL mRNA expression decreases upon stimulation of wild type (WT) bone marrow macrophages (BMMs) with RANKL, TAK1 deficiency in these cells leads to increased NUMBL and decreased TRAF6 and NEMO expression. These changes were restored upon WT-TAK1 expression, but not with catalytically inactive TAK1-K63W, suggesting that TAK1 enzymatic activity is required for these events. Forced expression of NUMBL inhibits osteoclast differentiation and function as evident by reduction in all hallmarks of osteoclastogenesis. Conversely, NUMBL-null BMMs, show increased osteoclast differentiation and mRNA expression of osteoclast marker genes. Post-translationally, K48-linked poly-ubiquitination of NUMBL is diminished in TAK1-null BMMs compared to elevated K48-poly-ubiquitination in WT cells, indicating increased stability of NUMBL in TAK1-null conditions. Further, our studies show that NUMBL directly interacts with TRAF6 and NEMO, and induces their K48-poly-ubiquitination mediated proteasomal degradation. Collectively, our data suggest that NUMBL and TAK1 are reciprocally regulated and that NUMBL acts as an endogenous regulator of NF-κB signaling and osteoclastogenesis by targeting the TAK1-TRAF6-NEMO axis.
NF-κB 信号通路对于破骨细胞分化和骨骼稳态至关重要。我们最近报道 NUMB 样蛋白(NUMBL)通过下调 NF-κB 激活来调节破骨细胞分化。在此,我们解析了这一现象的机制。我们发现,在 RANKL 刺激野生型(WT)骨髓巨噬细胞(BMM)时,NUMBL mRNA 表达降低,而这些细胞中 TAK1 的缺失导致 NUMBL 增加,TRAF6 和 NEMO 表达减少。这些变化在 WT-TAK1 表达时得到恢复,但在催化活性缺失的 TAK1-K63W 时则没有,这表明 TAK1 的酶活性对于这些事件是必需的。NUMBL 的强制表达抑制破骨细胞分化和功能,这表现在破骨细胞分化的所有标志均减少。相反,NUMBL 缺失的 BMM 显示出破骨细胞分化增加和破骨细胞标志物基因的 mRNA 表达增加。在翻译后水平上,与 WT 细胞中升高的 K48-多聚泛素化相比,TAK1 缺失的 BMM 中 NUMBL 的 K48 连接的多聚泛素化减少,表明在 TAK1 缺失条件下 NUMBL 的稳定性增加。此外,我们的研究表明,NUMBL 直接与 TRAF6 和 NEMO 相互作用,并诱导它们的 K48-多聚泛素化介导的蛋白酶体降解。总之,我们的数据表明 NUMBL 和 TAK1 是相互调节的,NUMBL 通过靶向 TAK1-TRAF6-NEMO 轴作为 NF-κB 信号和破骨细胞分化的内源性调节剂。