Dynamic Micropattern Geometry atop Shape Memory Polymers

K. A. Davis, J. H. Henderson
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引用次数: 1

Abstract

Substrates micropatterned with cell adhesion proteins have been used to investigate how protein density and geometry affect cell behaviors such as cell migration, growth, and differentiation. Existing technologies are limited in that they typically feature protein micropatterns that are static and unable to change while cells are attached. Here we micropatterned shape memory polymer (SMP) substrates that were capable of transitioning from a stretched state to a contracted state to control the width of patterned lines presented to attached cells. We found that micropattern geometry changed as the SMP substrate transitioned to its unstretched shape. Cells attached to dynamic patterns balled up and contracted their nuclei. The results suggest that micropatterned SMP cell culture substrates can be used to study the temporal aspects of cell mechanobiology.
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形状记忆聚合物上的动态微图案几何
细胞粘附蛋白微图纹底物已被用于研究蛋白质密度和几何形状如何影响细胞行为,如细胞迁移、生长和分化。现有技术的局限性在于,它们通常以蛋白质微模式为特征,这些模式是静态的,在细胞附着时无法改变。在这里,我们对形状记忆聚合物(SMP)衬底进行了微图纹处理,该衬底能够从拉伸状态过渡到收缩状态,以控制呈现给附着细胞的图纹线的宽度。我们发现,当SMP衬底过渡到未拉伸的形状时,微图案几何形状发生了变化。附着在动态模式上的细胞成团并收缩它们的细胞核。结果表明,微图案SMP细胞培养底物可用于研究细胞力学生物学的时间方面。
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