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卵清蛋白诱导的哮喘导致小鼠骨量流失并伴有Piezo通道抑制。

Ovalbumin-induced asthma leads to bone loss with Piezo channel suppression in mice.

作者信息

Gao Weiqi, Sawada Takeshi, Cao Ailin, Yoshimoto Reiko U, Yamaguchi Yu, Takahashi Yukie, Fukuda Takaichi, Ohsaki Yasuyoshi, Aijima Reona, Kadowaki Tomoko, Tsukuba Takayuki, Kido Mizuho A

机构信息

Division of Histology and Neuroanatomy, Department of Anatomy and Physiology, Faculty of Medicine, Saga University, Saga, Japan.

Department of Dental Pharmacology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.

出版信息

Commun Biol. 2025 Aug 29;8(1):1309. doi: 10.1038/s42003-025-08753-x.

Abstract

The impact of allergic diseases on bone loss remains unclear because it is considered to result from the use of corticosteroids to ameliorate allergic inflammation. To explore the effects of allergic diseases on bone metabolism, we investigated long bones in ovalbumin (OVA)-induced asthmatic mice. Compared with that of vehicle-treated controls, the bone mass of OVA-induced asthmatic mice was lower. We found fewer mature osteoblasts on the surfaces of the cortical and trabecular bones of allergen-sensitized mice than in those of vehicle-treated mice. Piezo1 and Piezo2 were located in mature osteoblasts, and their expression levels decrease during osteocytogenesis. Compared with that in non-asthmatic mice, the expression levels of both Piezo1 and Piezo2 were suppressed in asthmatic mice. The Piezo1 agonist reversed OVA-induced bone loss, with increased osteogenesis and type I collagen (Col1) expression. Furthermore, compared with control mice, Piezo2 heterozygous deletion mice with OVA presented a decreased bone volume. Our data suggest that asthma could induce osteopenia and that Piezo channel modulation could be a possible way to prevent bone loss induced by allergic asthma.

摘要

过敏性疾病对骨质流失的影响仍不明确,因为人们认为这是使用皮质类固醇来减轻过敏性炎症所致。为了探究过敏性疾病对骨代谢的影响,我们研究了卵清蛋白(OVA)诱导的哮喘小鼠的长骨。与接受载体处理的对照组相比,OVA诱导的哮喘小鼠的骨量较低。我们发现,致敏小鼠的皮质骨和小梁骨表面的成熟成骨细胞比接受载体处理的小鼠少。Piezo1和Piezo2位于成熟成骨细胞中,它们的表达水平在骨细胞生成过程中降低。与非哮喘小鼠相比,哮喘小鼠中Piezo1和Piezo2的表达水平均受到抑制。Piezo1激动剂可逆转OVA诱导的骨质流失,增加成骨作用和I型胶原蛋白(Col1)的表达。此外,与对照小鼠相比,患有OVA的Piezo2杂合缺失小鼠的骨体积减小。我们的数据表明,哮喘可诱发骨质减少,而调节Piezo通道可能是预防过敏性哮喘所致骨质流失的一种可行方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd9a/12397299/208ec436117e/42003_2025_8753_Fig1_HTML.jpg

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