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基于磷酸盐的玻璃微球上的干细胞长期培养:化学配方和 3D 结构的协同作用。

Long-Term Culture of Stem Cells on Phosphate-Based Glass Microspheres: Synergistic Role of Chemical Formulation and 3D Architecture.

机构信息

Wolfson Centre for Stem Cells, Tissue Engineering and Modelling (STEM), School of Medicine, University of Nottingham, Nottingham NG7 2RD, U.K.

Advanced Materials Research Group, Faculty of Engineering, University of Nottingham, Nottingham NG7 2RD, U.K.

出版信息

ACS Appl Bio Mater. 2021 Aug 16;4(8):5987-6004. doi: 10.1021/acsabm.1c00120. Epub 2021 Jul 29.

Abstract

Phosphate-based glasses (PBGs) are biomaterials that degrade under physiological conditions and can be modified to release various ions depending on end applications. This study utilized slow-degrading (P45:45PO-16CaO-24MgO-11NaO-4FeO, mol %) and comparatively faster degrading (P40:40PO-16CaO-24MgO-20NaO, mol %) PBG microspheres with or without porosity, to evaluate the combined effect of chemical formulation and geometry on human mesenchymal stem cells (MSCs), a clinically relevant cell source for orthopedic applications. Scanning electron microscopy showed 2, 46, and 29% of P45 bulk (P45-B), P40 bulk (P40-B), and P40 porous (P40-P) microspheres, respectively, that had cracks or peeling off surfaces after 42 days of incubation in culture medium. Cytotoxicity assessment showed that glass debris released into the culture medium may interact with cells and affect their survival. Direct-contact cell experiments up to 42 days showed that P45-B microspheres did not sustain viable long-term cell cultures and did not facilitate extracellular matrix formation. On the other hand, P40-B microspheres enhanced alkaline phosphatase activity, calcium deposition, and collagen and osteocalcin production in MSCs. Introduction of porosity in P40 glass further enhanced these parameters and proliferation at later time points. The small pore windows (<5 μm wide) and interconnection (<10 μm wide) may have allowed limited cell penetration into the porous structures. P40-B and P40-P have potential for bone repair and reinforcement therapy based on their chemical formulation and porous geometry.

摘要

基于磷酸盐的玻璃(PBG)是在生理条件下降解的生物材料,可以根据最终应用进行修改以释放各种离子。本研究利用降解速度较慢(P45:45PO-16CaO-24MgO-11NaO-4FeO,摩尔%)和相对较快降解(P40:40PO-16CaO-24MgO-20NaO,摩尔%)的 PBG 微球,有无孔结构,评估化学配方和几何形状对人骨髓间充质干细胞(MSCs)的综合影响,MSCs 是骨科应用中临床相关的细胞来源。扫描电子显微镜显示,在培养 42 天后,P45 块状(P45-B)、P40 块状(P40-B)和 P40 多孔(P40-P)微球的分别有 2%、46%和 29%的微球出现裂缝或表面剥落。细胞毒性评估表明,释放到培养基中的玻璃碎片可能与细胞相互作用并影响其存活。直接接触细胞实验长达 42 天表明,P45-B 微球不能维持长期存活的细胞培养,也不能促进细胞外基质的形成。另一方面,P40-B 微球增强了碱性磷酸酶活性、钙沉积以及 MSC 中胶原蛋白和骨钙素的产生。在 P40 玻璃中引入多孔结构进一步增强了这些参数和后期的增殖。小孔窗(<5μm 宽)和连通性(<10μm 宽)可能允许细胞有限地渗透到多孔结构中。基于其化学配方和多孔几何形状,P40-B 和 P40-P 具有用于骨修复和增强治疗的潜力。

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