HIF-1α介导破骨细胞诱导的小鼠股骨废用性骨质疏松症。

Bone Pub Date : 2022-12-01 DOI:10.2139/ssrn.4263596
M. Bie, Yi Tang, Yuxing Xia, Q. Zhang, Yuanye Tian, Chun Cheng, Xinzhao Li, Xin Qi, F. Kang
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引用次数: 1

摘要

由于卧床休息或航空航天等原因而导致的闲置性骨质疏松症已成为最常见的骨骼疾病之一。然而,废用性骨质疏松症的机制仍不清楚。我们在小鼠身上验证了悬尾模型,并证明在股骨小梁和皮质骨中存在骨质流失。重要的是,我们发现破骨细胞中缺氧诱导因子-1α (HIF-1α)的基因缺失改善了小梁骨中的破骨细胞骨吸收,而用HIF-1α抑制剂进行药物治疗可以保护后肢卸车小鼠免受小梁骨和皮质骨中废用性骨质疏松症的影响。HIF-1α敲除RAW264.7细胞和rna测序证明HIF-1α对破骨细胞发生和骨吸收至关重要,因为它通过细胞髓细胞瘤病(c-Myc)癌基因调节肌苷单磷酸脱氢酶(IMPDH)和胞苷三磷酸合成酶(CTPS)的水平。IMPDH和CTPS是重要的核苷酸代谢酶,在细胞代谢中起着重要的功能作用,它们可以在细胞内组装成线状或环状结构,以应对细胞应激。有趣的是,在体外和体内,破骨细胞中均发现了IMPDH和CTPS嗜细胞,HIF-1α水平与破骨细胞发生和骨吸收活性相关。我们的数据显示,在废用性骨质疏松症中,破骨细胞介导细胞代谢可能需要HIF-1α/c-Myc/嗜细胞瘤信号。总之,我们的研究结果揭示了HIF-1α/c-Myc/嗜细胞因子在支持破骨细胞发生和骨吸收中的新作用,并为其在废用性骨质疏松症发病机制中的作用提供了证据,这可能为治疗提供有希望的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HIF-1α mediates osteoclast-induced disuse osteoporosis via cytoophidia in the femur of mice.
Osteoporosis induced by disuse because of bed rest or the aerospace industry has become one of the most common skeletal disorders. However, mechanisms underlying the disuse osteoporosis remain largely unknown. We validated the tail-suspended model in mice and demonstrated that there is bone loss in the trabecular and cortical bones of the femur. Importantly, we showed that genetical deletion of hypoxia-inducible factor-1α (HIF-1α) in osteoclasts ameliorated osteoclastic bone resorption in the trabecular bone whereas pharmacological treatment with HIF-1α inhibitor protected the hindlimb-unloaded mice from disuse-induced osteoporosis in the trabecular and cortical bones. The HIF-1α knockout RAW264.7 cells and RNA-sequencing proved that HIF-1α is vital for osteoclastogenesis and bone resorption because it regulated the level of inosine monophosphate dehydrogenase (IMPDH) and cytidine triphosphate synthetase (CTPS) via cellular myelocytomatosis (c-Myc) oncogene. The IMPDH and CTPS are vital nucleotide metabolic enzymes which have an important functional role in cell metabolism, and they can assemble into intracellular linear or ring-shaped structures to cope with cell stress. Interestingly, both in vitro and in vivo, the IMPDH and CTPS cytoophidia were found in osteoclasts, and the level of HIF-1α correlated with osteoclastogenesis and bone-resorbing activity. Our data revealed that HIF-1α/c-Myc/cytoophidia signalling might be required for osteoclasts to mediate cell metabolism in disuse-induced osteoporosis. Overall, our results revealed a new role of HIF-1α/c-Myc/cytoophidia in supporting osteoclastogenesis and bone resorption and exposed evidence for its role in the pathogenesis of disuse osteoporosis, which might provide promising therapeutic targets.
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