Strontium zinc silicate simultaneously alleviates osteoporosis and sarcopenia in tail-suspended rats via Piezo1-mediated Ca2+ signaling

IF 5.9 1区 医学 Q1 ORTHOPEDICS Journal of Orthopaedic Translation Pub Date : 2024-08-13 DOI:10.1016/j.jot.2024.07.014
Lingwei Huang , Yiren Jiao , Hangbin Xia , Huili Li , Jing Yu , Yumei Que , Zhen Zeng , Chen Fan , Chen Wang , Chen Yang , Jiang Chang
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Abstract

Background

Long-term physical inactivity probably leads to a co-existence of osteoporosis and sarcopenia which result in a high risk of falls, fractures, disability and even mortality. However, universally applicable and feasible approaches are lacking in the concurrent treatment of osteoporosis and sarcopenia. In this study, we evaluated the effect of strontium zinc silicate bioceramic (SZS) extract on osteoporosis and sarcopenia and explored its underlying mechanisms.

Methods

Hindlimb osteoporosis and sarcopenia were established in a tail-suspended rat model. The bones were conducted μCT scanning, histological examination, and gene expression analysis, and the muscles were conducted histological examination and gene expression analysis. In vitro, the effect of SZS extract on osteoblasts was determined by alizarin red S staining, immunofluorescence and qPCR. Similarly, the effect of SZS extract on myoblasts was determined by immunofluorescence and qPCR.. At last, the role of Piezo1 and the change of intracellular calcium ion (Ca2+) were explored through blockading the Piezo1 by GsMTx4 in MC3T3-E1 and C2C12 cells, respectively.

Results

We found that SZS extract could concurrently and efficiently prevent bone structure deterioration, muscle atrophy and fibrosis in hind limbs of the tail-suspended rats. The in vivo study also showed that SZS extract could upregulate the mRNA expression of Piezo1, thereby maintaining the homeostasis of bones and muscles. In vitro study demonstrated that SZS extract could promote the proliferation and differentiation of MC3T3-E1 and C2C12 cells by increasing the intracellular Ca2+ in a Piezo1-dependent manner.

Conclusion

This study demonstrated that SZS extract could increase Piezo1-mediated intracellular Ca2+, and facilitate osteogenic differentiation of osteoblast and myogenic differentiation of myoblasts, contributing to alleviation of osteoporosis and sarcopenia in a tail-suspended rat model.

The translational potential of this article

The current study might provide a universally applicable and efficient strategy to treat musculoskeletal disorders based on bioactive ceramics. The verification of the role of Piezo1-modulated intracellular Ca2+ during osteogenesis and myogenesis provided a possible therapeutic target against mechanical related diseases.

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硅酸锶锌通过 Piezo1 介导的 Ca2+ 信号同时缓解尾悬大鼠的骨质疏松症和肌肉疏松症
背景长期缺乏运动可能会导致骨质疏松症和肌肉疏松症并存,从而导致跌倒、骨折、残疾甚至死亡的高风险。然而,在同时治疗骨质疏松症和肌肉疏松症方面缺乏普遍适用且可行的方法。本研究评估了硅酸锶锌生物陶瓷(SZS)提取物对骨质疏松症和肌肉疏松症的影响,并探讨了其潜在机制。对大鼠的骨骼进行了μCT扫描、组织学检查和基因表达分析,对肌肉进行了组织学检查和基因表达分析。在体外,通过茜素红 S 染色、免疫荧光和 qPCR 检测 SZS 提取物对成骨细胞的影响。同样,SZS 提取物对成肌细胞的影响也是通过免疫荧光和 qPCR 来确定的。结果我们发现,SZS 提取物能同时有效地防止尾悬大鼠后肢的骨结构退化、肌肉萎缩和纤维化。体内研究还表明,SZS 提取物能上调 Piezo1 的 mRNA 表达,从而维持骨骼和肌肉的平衡。体外研究表明,SZS 提取物能以 Piezo1 依赖性方式通过增加细胞内 Ca2+ 促进 MC3T3-E1 和 C2C12 细胞的增殖和分化。结论本研究表明,SZS 提取物能增加 Piezo1 介导的细胞内 Ca2+,促进成骨细胞的成骨分化和成肌细胞的成肌分化,有助于缓解尾悬大鼠模型的骨质疏松症和肌肉疏松症。Piezo1调控细胞内Ca2+在成骨和成肌过程中的作用得到了验证,为治疗机械相关疾病提供了可能的靶点。
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来源期刊
Journal of Orthopaedic Translation
Journal of Orthopaedic Translation Medicine-Orthopedics and Sports Medicine
CiteScore
11.80
自引率
13.60%
发文量
91
审稿时长
29 days
期刊介绍: The Journal of Orthopaedic Translation (JOT) is the official peer-reviewed, open access journal of the Chinese Speaking Orthopaedic Society (CSOS) and the International Chinese Musculoskeletal Research Society (ICMRS). It is published quarterly, in January, April, July and October, by Elsevier.
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