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通过巯基-烯点击化学将 PEG 微凝胶组装成多孔的细胞指导性 3D 支架。

Assembly of PEG Microgels into Porous Cell-Instructive 3D Scaffolds via Thiol-Ene Click Chemistry.

机构信息

Department of Biomedical Engineering, Texas A&M University, College Station, TX, 77843, USA.

Department of Materials Science and Engineering, Texas A&M University, College Station, TX, 77843, USA.

出版信息

Adv Healthc Mater. 2018 Jun;7(11):e1800160. doi: 10.1002/adhm.201800160. Epub 2018 Apr 16.

Abstract

The assembly of microgel building blocks into 3D scaffolds is an emerging strategy for tissue engineering. A key advantage is that the inherent microporosity of these scaffolds provides cells with a more permissive environment than conventional nanoporous hydrogels. Here, norbornene-bearing poly(ethylene glycol) (PEG) based microgels are assembled into 3D cell-instructive scaffolds using a PEG-dithiol linker and thiol-ene click photopolymerization. The bulk modulus of these materials depends primarily on the crosslink density of the microgel building blocks. However, the linker and initiator concentrations used during assembly have significant effects on cell spreading and proliferation when human mesenchymal stem cells (hMSCs) are incorporated in the scaffolds. The cell response is also affected by the properties of the modular microgel building blocks, as hMSCs growing in scaffolds assembled from stiff but not soft microgels activate Yes-associated protein signaling. These results indicate that PEG microgel scaffolds assembled via thiol-ene click chemistry can be engineered to provide a cell-instructive 3D milieu, making them a promising 3D platform for tissue engineering.

摘要

将微凝胶构建块组装成 3D 支架是组织工程的一种新兴策略。一个关键优势是,这些支架的固有微孔性为细胞提供了比传统纳米多孔水凝胶更宽松的环境。在这里,通过 PEG-二硫醇接头和硫醇-烯点击光聚合作用,将含有降冰片烯的聚乙二醇(PEG)基微凝胶组装成 3D 细胞指令性支架。这些材料的体积模量主要取决于微凝胶构建块的交联密度。然而,当人骨髓间充质干细胞(hMSCs)被掺入支架中时,组装过程中使用的接头和引发剂浓度对细胞扩散和增殖有显著影响。细胞反应也受到模块化微凝胶构建块性质的影响,因为在由刚性但不柔软的微凝胶组装的支架中生长的 hMSCs 激活了 Yes 相关蛋白信号。这些结果表明,通过硫醇-烯点击化学组装的 PEG 微凝胶支架可以进行工程设计,以提供细胞指令性的 3D 环境,使它们成为组织工程有前途的 3D 平台。

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