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Mechanically- Biologically-Tunable Polyethylene Glycol Hydrogels for Quantitative Neutrophil Migration Assays

机译:机械可调和生物可调的聚乙二醇水凝胶用于中性粒细胞迁移定量分析

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Porated PEG gels can be used for modular, biomimetic. immunoassays to replicate the complexity and diversity of human ECM in vitro. Urea salt leached PEG gels serve as mechanistic models to explore chemotaxis in 3D ECM, such as interstitial tissue. Using these gels, we demonstrate that within a physiological range of soft tissues (<5 kPa), less stiff (lower Young's moduli), more locally elastic gels (higher PEG MW) are more supportive of PMN migration. Similarly, small pores and high pore densities further promote PMN chemotaxis in response to IL-8. We confirmed prior results showing that a dearth or an excess of cell binding sites reduces chemotaxis. We next presented thinner, porated gels that replicate specialized ECM, such as vascular BM. These gels offer mechanical and biological advantages to current models, i.e. TWs, while maintaining their thin structure. Overall, PEG gels improve in vitro ECM models and provide more relevant results of immune cell migration in mechanically and biologically complex settings.
机译:多孔PEG凝胶可用于模块化仿生。免疫测定法可在体外复制人类ECM的复杂性和多样性。尿素盐浸出的PEG凝胶用作探索3D ECM(例如间质组织)趋化性的机制模型。使用这些凝胶,我们证明了在软组织的生理范围内(<5 kPa),硬度较小(杨氏模量较低),局部弹性较大的凝胶(较高PEG MW)更能支持PMN迁移。同样,小孔和高孔密度进一步促进PMN对IL-8的趋化性。我们证实了先前的结果,表明缺乏或过量的细胞结合位点会降低趋化性。接下来,我们介绍了可以复制专门的ECM(例如血管BM)的更薄,多孔的凝胶。这些凝胶在保持其薄型结构的同时,为目前的型号,即TWs提供了机械和生物学优势。总体而言,PEG凝胶改善了体外ECM模型,并在机械和生物复杂的环境中提供了免疫细胞迁移的更多相关结果。

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