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Hydrogel scaffolds to study cell biology in four dimensions

机译:水凝胶支架体外研究细胞生物学四个维度

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摘要

Poly(ethylene glycol) (PEG) hydrogels represent a versatile material scaffold for culturing cells in two or three dimensions with the advantages of limited protein fouling and cytocompatible polymerization to enable cell encapsulation. By using light-based chemistries for gelation and for incorporating biomolecules into the network, dynamic niches can be created that facilitate the study of how cells respond to user-dictated or cell-dictated changes in environmental signals. Specifically, we demonstrate integration of a photo-cleavable molecule into network cross-links and into pendant functional groups to construct gels with biophysical and biochemical properties that are spatiotemporally tunable with light. Complementary to this approach, an enzymatically cleavable peptide sequence can be introduced within hydrogel networks, in this case through photoinitiated addition reactions between thiol-containing biomacromolecules and ene-containing synthetic polymers, to enable cellular remodeling of their surrounding hydrogel microenvironment. With such tunable material platforms, researchers can employ a systematic approach for 3D cell culture experiments, spatially and temporally modulating physical properties (e.g., stiffness) as well as biological signals (e.g., adhesive ligands) to study cell behavior in response to environmental stimuli. Collectively, these material systems suggest routes for new experimentation to study and manipulate cellular functions in four dimensions.
机译:聚(乙二醇)(PEG)水凝胶代表了一种通用的材料支架,可用于二维或三维培养细胞,其优点是蛋白质结垢和细胞相容性聚合作用有限,可实现细胞封装。通过使用基于光的化学方法进行凝胶化并将生物分子整合到网络中,可以创建动态壁ches,从而有利于研究细胞如何响应用户指示或细胞指示的环境信号变化。具体来说,我们展示了将光可裂解分子整合到网络交联和侧链官能团中,以构建具有光时空可调的生物物理和生化特性的凝胶。作为该方法的补充,可以在水凝胶网络内引入酶促可裂解的肽序列,在这种情况下,是通过含硫醇的生物大分子与含烯的合成聚合物之间的光引发加成反应,从而使其周围的水凝胶微环境发生细胞重塑。借助这样的可调材料平台,研究人员可以采用系统的方法进行3D细胞培养实验,在空间和时间上调节物理特性(例如刚度)和生物信号(例如粘性配体),以研究响应环境刺激的细胞行为。总的来说,这些物质系统为新的实验提供了途径,以研究和操纵四个维度的细胞功能。

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  • 年(卷),期 -1(38),3
  • 年度 -1
  • 页码 260–268
  • 总页数 20
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