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基于材料的纤连蛋白在纳米形貌上的组装增强了间充质干细胞的黏附性,保护细胞免受细菌毒力因子的侵害,并防止生物膜的形成。

Materials-driven fibronectin assembly on nanoscale topography enhances mesenchymal stem cell adhesion, protecting cells from bacterial virulence factors and preventing biofilm formation.

机构信息

Department of Biology, Collage of Science, University of Jeddah, Jeddah, 23890, Saudi Arabia; Centre for the Cellular Microenvironment, Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, G12 8QQ, UK.

Centre for the Cellular Microenvironment, Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, G12 8QQ, UK.

出版信息

Biomaterials. 2022 Jan;280:121263. doi: 10.1016/j.biomaterials.2021.121263. Epub 2021 Nov 17.

Abstract

Post-operative infection is a major complication in patients recovering from orthopaedic surgery. As such, there is a clinical need to develop biomaterials for use in regenerative surgery that can promote mesenchymal stem cell (MSC) osteospecific differentiation and that can prevent infection caused by biofilm-forming pathogens. Nanotopographical approaches to pathogen control are being identified, including in orthopaedic materials such as titanium and its alloys. These topographies use high aspect ratio nanospikes or nanowires to prevent bacterial adhesion but these features also significantly reduce MSC adhesion and activity. Here, we use a poly (ethyl acrylate) (PEA) polymer coating on titanium nanowires to spontaneously organise fibronectin (FN) and to deliver bone morphogenetic protein 2 (BMP2) to enhance MSC adhesion and osteospecific signalling. Using a novel MSC-Pseudomonas aeruginosa co-culture, we show that the coated nanotopographies protect MSCs from cytotoxic quorum sensing and signalling molecules, enhance MSC adhesion and osteoblast differentiation and reduce biofilm formation. We conclude that the PEA polymer-coated nanotopography can both support MSCs and prevent pathogens from adhering to a biomaterial surface, thus protecting from biofilm formation and bacterial infection, and supporting osteogenic repair.

摘要

术后感染是骨科手术后患者的主要并发症。因此,临床上需要开发可用于再生手术的生物材料,这些材料既能促进间充质干细胞(MSC)成骨特异性分化,又能预防生物膜形成病原体引起的感染。目前正在确定用于病原体控制的纳米拓扑方法,包括钛及其合金等骨科材料。这些拓扑结构使用高纵横比纳米尖峰或纳米线来防止细菌附着,但这些特征也会显著降低 MSC 的附着和活性。在这里,我们使用聚(丙烯酸乙酯)(PEA)聚合物在钛纳米线上进行涂层,以自发组织纤连蛋白(FN)并递送骨形态发生蛋白 2(BMP2),以增强 MSC 的附着和成骨特异性信号传导。使用新型 MSC-铜绿假单胞菌共培养物,我们表明涂层的纳米形貌可保护 MSC 免受细胞毒性群体感应和信号分子的侵害,增强 MSC 附着和成骨细胞分化,并减少生物膜形成。我们得出结论,PEA 聚合物涂层的纳米形貌既能支持 MSC,又能防止病原体附着在生物材料表面,从而防止生物膜形成和细菌感染,并支持成骨修复。

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