Hao Xiaoxia, Wang Dan, Yan Zedong, Ding Yuanjun, Zhang Juan, Liu Juan, Shao Xi, Liu Xiyu, Wang Lu, Luo Erping, Cai Jing, Jing Da
School of Life Science, Northwest University, Xi'an, China.
Department of Biomedical Engineering, Fourth Military Medical University, Xi'an, China.
J Bone Miner Res. 2023 Apr;38(4):597-614. doi: 10.1002/jbmr.4772. Epub 2023 Feb 13.
Chronic high-altitude hypoxia induces irreversible abnormalities in various organisms. Emerging evidence indicates that hypobaric hypoxia markedly suppresses bone mass and bone strength. However, few effective means have been identified to prevent such bone deficits. Here, we assessed the potential of pulsed electromagnetic fields (PEMFs) to noninvasively resist bone deterioration induced by hypobaric hypoxia. We observed that exogenous PEMF treatment at 15 Hz and 20 Gauss (Gs) improved the cancellous and cortical bone mass, bone microstructure, and skeletal mechano-properties in rats subjected to chronic exposure of hypobaric hypoxia simulating an altitude of 4500 m for 6 weeks by primarily modulating osteoblasts and osteoblast-mediated bone-forming activity. Moreover, our results showed that whereas PEMF stimulated the functional activity of primary osteoblasts in hypoxic culture in vitro, it had negligible effects on osteoclasts and osteocytes exposed to hypoxia. Mechanistically, the primary cilium was found to function as the major electromagnetic sensor in osteoblasts exposed to hypoxia. The polycystins PC-1/PC-2 complex was identified as the primary calcium channel in the primary cilium of hypoxia-exposed osteoblastic cells responsible for the detection of external PEMF signals, and thereby translated these biophysical signals into intracellular biochemical events involving significant increase in the intracellular soluble adenylyl cyclase (sAC) expression and subsequent elevation of cyclic adenosine monophosphate (cAMP) concentration. The second messenger cAMP inhibited the transcription of oxygen homeostasis-related hypoxia-inducible factor 1-alpha (HIF-1α), and thus enhanced osteoblast differentiation and improved bone phenotype. Overall, the present study not only advances our understanding of bone physiology at high altitudes, but more importantly, proposes effective means to ameliorate high altitude-induced bone loss in a noninvasive and cost-effective manner. © 2023 American Society for Bone and Mineral Research (ASBMR).
慢性高原缺氧会在各种生物体中引发不可逆的异常。新出现的证据表明,低压缺氧会显著抑制骨量和骨强度。然而,几乎没有发现有效的方法来预防这种骨质缺陷。在此,我们评估了脉冲电磁场(PEMFs)无创抵抗低压缺氧诱导的骨质恶化的潜力。我们观察到,以15赫兹和20高斯(Gs)进行外源性PEMF治疗,通过主要调节成骨细胞和成骨细胞介导的骨形成活性,改善了模拟海拔4500米慢性暴露于低压缺氧6周的大鼠的松质骨和皮质骨量、骨微结构以及骨骼力学性能。此外,我们的结果表明,虽然PEMF在体外缺氧培养中刺激了原代成骨细胞的功能活性,但对暴露于缺氧环境的破骨细胞和骨细胞影响可忽略不计。从机制上讲,初级纤毛被发现是暴露于缺氧环境的成骨细胞中的主要电磁传感器。多囊蛋白PC - 1/PC - 2复合物被确定为暴露于缺氧环境的成骨细胞初级纤毛中的主要钙通道,负责检测外部PEMF信号,从而将这些生物物理信号转化为细胞内生化事件,包括细胞内可溶性腺苷酸环化酶(sAC)表达显著增加以及随后环磷酸腺苷(cAMP)浓度升高。第二信使cAMP抑制氧稳态相关的缺氧诱导因子1 - α(HIF - 1α)的转录,从而增强成骨细胞分化并改善骨表型。总体而言,本研究不仅增进了我们对高原骨生理学的理解,更重要的是,提出了以无创且经济有效的方式改善高原诱导性骨质流失的有效方法。© 2023美国骨与矿物质研究学会(ASBMR)