Department of Biomedical Engineering, Columbia University, New York, NY, USA.
J Bone Miner Res. 2022 May;37(5):972-982. doi: 10.1002/jbmr.4536. Epub 2022 Mar 23.
Bone cells actively respond to mechanical stimuli to direct bone formation, yet there is no current treatment strategy for conditions of low bone mass and osteoporosis designed to target the inherent mechanosensitivity of bone. Our group has previously identified the primary cilium as a critical mechanosensor within bone, and that pharmacologically targeting the primary cilium with fenoldopam can enhance osteocyte mechanosensitivity. Here, we demonstrate that potentiating osteocyte mechanosensing with fenoldopam in vitro promotes pro-osteogenic paracrine signaling to osteoblasts. Conversely, impairing primary cilia formation and the function of key ciliary mechanotransduction proteins attenuates this intercellular signaling cascade. We then utilize an in vivo model of load-induced bone formation to demonstrate that fenoldopam treatment sensitizes bones of both healthy and osteoporotic mice to mechanical stimulation. Furthermore, we show minimal adverse effects of this treatment and demonstrate that prolonged treatment biases trabecular bone adaptation. This work is the first to examine the efficacy of targeting primary cilia-mediated mechanosensing to enhance bone formation in osteoporotic animals. © 2022 American Society for Bone and Mineral Research (ASBMR).
骨细胞对机械刺激做出积极响应,从而指导骨形成,但目前还没有针对低骨量和骨质疏松症的治疗策略,旨在针对骨的固有机械敏感性。我们的研究小组先前已经确定初级纤毛是骨内的关键机械感受器,并且用非诺多泮药理学靶向初级纤毛可以增强成骨细胞的机械敏感性。在这里,我们证明体外用非诺多泮增强成骨细胞的机械敏感性可促进成骨细胞的旁分泌信号传递至成骨细胞。相反,破坏初级纤毛的形成和关键纤毛机械转导蛋白的功能会削弱这种细胞间信号级联。然后,我们利用负载诱导骨形成的体内模型证明,非诺多泮治疗可使健康和骨质疏松小鼠的骨骼对机械刺激敏感。此外,我们还表明这种治疗的副作用很小,并证明了长期治疗会使小梁骨适应产生偏差。这项工作首次检查了靶向初级纤毛介导的机械敏感性以增强骨质疏松动物骨形成的功效。 © 2022 美国骨矿研究协会(ASBMR)。