Clinical Research Platform for Interdiscipline of Stomatology, The First Affiliated Hospital of Jinan University & Department of Stomatology, College of stomatology, Jinan University, Guangzhou, China.
Beijing Advanced Innovation Center for Big Data-Based Precision Medicine, School of Engineering Medicine, Beihang University, Beijing, China.
Nat Commun. 2021 Jun 3;12(1):3319. doi: 10.1038/s41467-021-23642-7.
Long noncoding RNAs are widely implicated in diverse disease processes. Nonetheless, their regulatory roles in bone resorption are undefined. Here, we identify lncRNA Nron as a critical suppressor of bone resorption. We demonstrate that osteoclastic Nron knockout mice exhibit an osteopenia phenotype with elevated bone resorption activity. Conversely, osteoclastic Nron transgenic mice exhibit lower bone resorption and higher bone mass. Furthermore, the pharmacological overexpression of Nron inhibits bone resorption, while caused apparent side effects in mice. To minimize the side effects, we further identify a functional motif of Nron. The delivery of Nron functional motif to osteoclasts effectively reverses bone loss without obvious side effects. Mechanistically, the functional motif of Nron interacts with E3 ubiquitin ligase CUL4B to regulate ERα stability. These results indicate that Nron is a key bone resorption suppressor, and the lncRNA functional motif could potentially be utilized to treat diseases with less risk of side effects.
长链非编码 RNA 广泛参与多种疾病过程。然而,它们在骨吸收中的调节作用尚未明确。在这里,我们鉴定出 lncRNA Nron 是骨吸收的关键抑制因子。我们证明破骨细胞 Nron 敲除小鼠表现出骨质疏松表型,骨吸收活性升高。相反,破骨细胞 Nron 转基因小鼠表现出较低的骨吸收和更高的骨量。此外,Nron 的药理学过表达抑制骨吸收,而在小鼠中引起明显的副作用。为了最小化副作用,我们进一步鉴定了 Nron 的功能基序。将 Nron 功能基序递送至破骨细胞可有效逆转骨丢失,而无明显副作用。在机制上,Nron 的功能基序与 E3 泛素连接酶 CUL4B 相互作用,以调节 ERα 的稳定性。这些结果表明,Nron 是一种关键的骨吸收抑制因子,lncRNA 功能基序可能可用于治疗疾病,副作用风险较低。