Fabrication of Lithium/Strontium-Releasing Smart Bioactive Glasses with Anti-Inflammatory and Osteogenic Effects Tailored to Pathological Stages.

IF 4.1 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hirohiko Sakai, Jun-Ichi Sasaki, Haruaki Kitagawa, Gabriela L Abe, Tomoki Kohno, Naoya Funayama, Satoshi Imazato
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引用次数: 0

Abstract

Bioactive glasses (BGs) are highly biocompatible with affinity for hard tissues and exhibit high bioactivity through ion release. Smart BGs that allow controlled ion release are required because uncontrolled release can lead to unexpected adverse effects on tissue regeneration. Strontium promotes osteoblast differentiation of mesenchymal stem cells (MSCs) and inhibits osteoclast activity. In this study, the release profile of strontium is regulated by the incorporation of aluminum into a phosphate-based BG. Furthermore, composites of strontium-releasing BG and lithium-releasing BG (Li/Sr-BG) show stepwise ion release, with rapid lithium release followed by sustained strontium release. Li/Sr-BG increases the expression of osteogenic markers and mineral deposition in MSCs, but suppresses osteoclast maturation, including multinucleation and osteoclast marker expression. Additionally, application of Li/Sr-BG to inflammatory macrophages decreases phagocytic activity and inflammatory gene expression, while increasing the expression of anti-inflammatory markers. Analysis of signaling proteins reveals that osteogenic and anti-inflammatory effects of Li/Sr-BG are attributed to the release of strontium and lithium, respectively. This study demonstrates that Li/Sr-BGs can be used for the development of novel smart bioactive materials that effectively suppress inflammation and promote bone formation in a manner that follows the process of bone regeneration.

具有抗炎和成骨作用的锂/锶释放智能生物活性眼镜的制备
生物活性玻璃(BGs)具有高度的生物相容性和对硬组织的亲和力,并通过离子释放表现出很高的生物活性。由于不受控制的离子释放会对组织再生产生意想不到的不利影响,因此需要能够控制离子释放的智能bg。锶促进间充质干细胞(MSCs)的成骨细胞分化并抑制破骨细胞活性。在这项研究中,锶的释放轮廓是通过铝掺入磷酸盐基BG来调节的。此外,锶释放BG和锂释放BG复合材料(Li/Sr-BG)的离子释放呈阶梯状,锂快速释放,锶持续释放。Li/Sr-BG增加MSCs中成骨标志物的表达和矿物质沉积,但抑制破骨细胞成熟,包括多核和破骨细胞标志物的表达。此外,Li/Sr-BG对炎性巨噬细胞的作用降低了吞噬活性和炎症基因表达,同时增加了抗炎标志物的表达。信号蛋白分析显示Li/Sr-BG的成骨和抗炎作用分别归因于锶和锂的释放。该研究表明,Li/Sr-BGs可用于开发新型智能生物活性材料,有效抑制炎症并促进骨形成,遵循骨再生过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Macromolecular bioscience
Macromolecular bioscience 生物-材料科学:生物材料
CiteScore
7.90
自引率
2.20%
发文量
211
审稿时长
1.5 months
期刊介绍: Macromolecular Bioscience is a leading journal at the intersection of polymer and materials sciences with life science and medicine. With an Impact Factor of 2.895 (2018 Journal Impact Factor, Journal Citation Reports (Clarivate Analytics, 2019)), it is currently ranked among the top biomaterials and polymer journals. Macromolecular Bioscience offers an attractive mixture of high-quality Reviews, Feature Articles, Communications, and Full Papers. With average reviewing times below 30 days, publication times of 2.5 months and listing in all major indices, including Medline, Macromolecular Bioscience is the journal of choice for your best contributions at the intersection of polymer and life sciences.
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