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首页> 外文期刊>Acta biomaterialia >Cellular responses to thermoresponsive stiffness memory elastomer nanohybrid scaffolds by 3D-TIPS
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Cellular responses to thermoresponsive stiffness memory elastomer nanohybrid scaffolds by 3D-TIPS

机译:通过3D尖端对热敏刚度记忆弹性体纳米混合物支架的细胞响应

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摘要

Increasing evidence suggests the contribution of the dynamic mechanical properties of the extracellular matrix (ECM) to regulate tissue remodeling and regeneration. Following our recent study on a family of thermoresponsive 'stiffness memory' elastomeric nanohybrid scaffolds manufactured via an indirect 3D printing guided thermally-induced phase separation process (3D-TIPS), this work reports in vitro and in vivo cellular responses towards these scaffolds with different initial stiffness and hierarchically interconnected porous structure. The viability of mouse embryonic dermal fibroblasts in vitro and the tissue responses during the stiffness softening of the scaffolds subcutaneously implanted in rats for three months were evaluated by immunohistochemistry and histology. Scaffolds with a higher initial stiffness and a hierarchical porous structure outperformed softer ones, providing initial mechanical support to cells and surrounding tissues before promoting cell and tissue growth during stiffness softening. Vascularization was guided throughout the digitally printed interconnected networks. All scaffolds exhibited polarization of the macrophage response from a macrophage phenotype type I (M1) towards a macrophage phenotype type II (M2) and down-regulation of the T-cell proliferative response with increasing implantation time; however, scaffolds with a more pronounced thermo-responsive stiffness memory mechanism exerted higher inflammo-informed effects. These results pave the way for personalized and biologically responsive soft tissue implants and implantable device with better mechanical matches, angiogenesis and tissue integration.
机译:越来越多的证据表明细胞外基质(ECM)的动态力学性能促进组织重塑和再生的贡献。在我们最近关于通过间接3D印刷引导的热诱导的相分离过程(3D-TIP)制造的热响应性“刚度记忆”弹性体纳米羊底的弹性纳米混合物进行研究,这项工作在体外报告并以不同的方式对这些支架进行体外响应初始刚度和分层互连的多孔结构。通过免疫组织化学和组织学评估小鼠胚胎皮肤体体外体外的活力和组织反应期间的刚性植入大鼠三个月的支架中的刚性软化。具有较高初始刚度和分层多孔结构的支架优于更柔软的刚度,在促进细胞和刚度软化期间的组织生长之前,为细胞和周围组织提供初始机械支撑。在整个数字印刷的互联网络中引导血管化。所有支架从巨噬细胞表型I(M1)朝向巨噬细胞表型II(M2)的偏振表现出巨噬细胞反应的偏振,以及随着植入时间的增加,T细胞增殖反应的下调;然而,具有更明显的热响应刚度记忆机制的支架施加了更高的炎症知识效果。这些结果为个性化和生物响应性软组织植入物和可植入装置铺平了道路,具有更好的机械匹配,血管生成和组织整合。

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