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可注射的有机/无机微流控微球促进骨修复的免疫生物学与生物信息学分析。

Immunology and bioinformatics analysis of injectable organic/inorganic microfluidic microspheres for promoting bone repair.

机构信息

Department of Orthopedics, The First Affiliated Hospital of Soochow University, Orthopedic Institute, Soochow University, 188 Shizi Road, Suzhou, Jiangsu, 215006, PR China.

Department of Orthopaedics, Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases, Shanghai Institute of Traumatology and Orthopaedics, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin 2nd Road, Shanghai, 200025, PR China.

出版信息

Biomaterials. 2022 Sep;288:121685. doi: 10.1016/j.biomaterials.2022.121685. Epub 2022 Jul 18.

Abstract

Organic/inorganic composites have advantages in promoting bone repair; however, early changes in the local immune response after material implantation and the mechanisms that affect the late osteogenesis have not been revealed systematically. Herein, we prepared injectable composite poly (l-lactic acid)/nano hydroxyapatite (PLLA/nHA) porous microspheres (MS@SL@nHA) using a microfluidic technology to explore the changes in the osteo-immune microenvironment and potential mechanisms using immunology and bioinformatics. Immunological analysis revealed that macrophages (Mφ) phagocytosed the nHA released from the composite microspheres, increased the proportion of M2 Mφ, regulated the early inflammatory response, exerted strong paracrine effects, and improved the osteo-immune microenvironment. Bioinformatics analysis showed that the signal transduction and adhesion ability were enhanced after Mφ activation, the inflammatory signaling pathways were inhibited, regulating the polarization direction, and the expression of cell growth factors was up-regulated to promote late osteogenesis. In vivo studies demonstrated that the composite microspheres effectively regulated Mφ polarization, and the paracrine secreted growth factors created a microsphere-centered osteogenesis pattern at the defect site. In conclusion, we successfully prepared injectable composite PLLA/nHA porous microspheres and systematically explored the osteogenesis-related mechanisms using immunological and bioinformatics analysis to provide theoretical evidence for bone repair materials that contribute to bone differentiation.

摘要

有机/无机复合材料在促进骨修复方面具有优势;然而,材料植入后局部免疫反应的早期变化以及影响晚期成骨的机制尚未系统揭示。在此,我们使用微流控技术制备了可注射的复合聚(L-乳酸)/纳米羟基磷灰石(PLLA/nHA)多孔微球(MS@SL@nHA),通过免疫学和生物信息学探索骨免疫微环境的变化和潜在机制。免疫分析表明,巨噬细胞(Mφ)吞噬复合微球中释放的 nHA,增加 M2 Mφ的比例,调节早期炎症反应,发挥强大的旁分泌作用,改善骨免疫微环境。生物信息学分析表明,Mφ激活后信号转导和黏附能力增强,炎症信号通路被抑制,调节极化方向,细胞生长因子的表达上调,促进晚期成骨。体内研究表明,复合微球可有效调节 Mφ的极化,旁分泌的生长因子在缺陷部位形成以微球为中心的成骨模式。总之,我们成功制备了可注射的复合 PLLA/nHA 多孔微球,并通过免疫学和生物信息学分析系统地探讨了成骨相关机制,为促进骨分化的骨修复材料提供了理论依据。

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