Suppr超能文献

原位酶反应生成具有优异生物活性的镁基矿化微球,增强骨再生。

In Situ Enzymatic Reaction Generates Magnesium-Based Mineralized Microspheres with Superior Bioactivity for Enhanced Bone Regeneration.

机构信息

Department of Orthopedics, Second Affiliated Hospital, Naval Medical University, Shanghai, 200003, P. R. China.

Center for Orthopedic Science and Translational Medicine, Department of Orthopedics, Shanghai Tenth People's Hospital, School of Medicine, Tongji University, Shanghai, 200072, P. R. China.

出版信息

Adv Healthc Mater. 2023 Sep;12(24):e2300727. doi: 10.1002/adhm.202300727. Epub 2023 Jun 20.

Abstract

Bone is a naturally mineralized tissue with a remarkable hierarchical structure, and the treatment of bone defects remains challenging. Microspheres with facile features of controllable size, diverse morphologies, and specific functions display amazing potentials for bone regeneration. Herein, inspired by natural biomineralization, a novel enzyme-catalyzed reaction is reported to prepare magnesium-based mineralized microspheres. First, silk fibroin methacryloyl (SilMA) microspheres are prepared using a combination of microfluidics and photo-crosslinking. Then, the alkaline phosphatase (ALP)-catalyzed hydrolysis of adenosine triphosphate (ATP) is successfully used to induce the formation of spherical magnesium phosphate (MgP) in the SilMA microspheres. These SilMA@MgP microspheres display uniform size, rough surface structure, good degradability, and sustained Mg release properties. Moreover, the in vitro studies demonstrate the high bioactivities of SilMA@MgP microspehres in promoting the proliferation, migration, and osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs). Transcriptomic analysis shows that the osteoinductivity of SilMA@MgP microspheres may be related to the activation of the PI3K/Akt signaling pathway. Finally, the bone regeneration enhancement units (BREUs) are designed and constructed by inoculating BMSCs onto SilMA@MgP microspheres. In summary, this study demonstrates a new biomineralization strategy for designing biomimetic bone repair materials with defined structures and combination functions.

摘要

骨是一种具有显著层次结构的天然矿化组织,骨缺损的治疗仍然具有挑战性。具有易于控制尺寸、多样形貌和特定功能的微球显示出在骨再生方面的巨大潜力。受天然生物矿化的启发,本研究报道了一种新型酶催化反应,用于制备基于镁的矿化微球。首先,采用微流控和光交联的方法制备丝素蛋白甲基丙烯酰(SilMA)微球。然后,成功地利用碱性磷酸酶(ALP)催化三磷酸腺苷(ATP)的水解,在 SilMA 微球中诱导形成球形磷酸镁(MgP)。这些 SilMA@MgP 微球具有均匀的尺寸、粗糙的表面结构、良好的降解性和持续的 Mg 释放性能。此外,体外研究表明 SilMA@MgP 微球具有促进骨髓间充质干细胞(BMSCs)增殖、迁移和成骨分化的高生物活性。转录组分析表明,SilMA@MgP 微球的成骨活性可能与 PI3K/Akt 信号通路的激活有关。最后,通过将 BMSCs 接种到 SilMA@MgP 微球上,设计并构建了骨再生增强单元(BREUs)。总之,本研究展示了一种新的生物矿化策略,用于设计具有定义结构和组合功能的仿生骨修复材料。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验