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Cell Adhesion on Micro-Structured Fibronectin Gradients Fabricated by Multiphoton Excited Photochemistry

机译:Multiboton兴奋光化学制造的微结构化纤维凝集素梯度上的细胞粘附

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摘要

Concentration gradients of ECM proteins play active roles in many areas of cell biology including wound healing and metastasis. They may also form the basis of tissue engineering scaffolds, as these can direct cell adhesion and migration and promote new matrix synthesis. To better understand cell–matrix interactions on attractive gradients, we have used multiphoton excited (MPE) photochemistry to fabricate covalently linked micro-structured gradients from fibronectin (FN). The gradient design is comprised of a parallel series of individual linear gradients with overall dimensions of approximately 800 × 800 μm, where a linear dynamic range of nearly 10-fold in concentration was achieved. The adhesion dynamics of 3T3 fibroblasts were investigated, where the cell morphology and actin cytoskeleton became increasingly elongated and aligned with the direction of the gradient at increasing protein concentration. Moreover, the cell morphologies are distinct when adhered to regions of differing FN concentration but with similar topography. These results show that the fabrication approach allows investigating the roles of contact guidance and ECM cues on the cell–matrix interactions. We suggest this design overcomes some of the limitations with other fabrication methods, especially in terms of 3D patterning capabilities, and will serve as a new tool to study cell–matrix interactions.
机译:ECM蛋白的浓度梯度在细胞生物学的许多领域都发挥着积极作用,包括伤口愈合和转移。它们也可能构成组织工程支架的基础,因为它们可以指导细胞粘附和迁移并促进新的基质合成。为了更好地理解有吸引力的梯度上的细胞-基质相互作用,我们使用了多光子激发(MPE)光化学从纤连蛋白(FN)制备共价连接的微结构梯度。梯度设计由一系列平行的单个线性梯度组成,总尺寸约为800×800μm,其中线性动态范围的浓度达到了近10倍。研究了3T3成纤维细胞的黏附动力学,其中细胞形态和肌动蛋白细胞骨架逐渐伸长,并在蛋白质浓度增加时与梯度方向一致。此外,当细胞粘附在不同FN浓度但具有相似形貌的区域时,细胞的形态是不同的。这些结果表明,这种制造方法可以研究接触指导和ECM提示在细胞-基质相互作用中的作用。我们建议这种设计克服了其他制造方法的某些局限性,特别是在3D图案化能力方面,并将成为研究细胞-基质相互作用的新工具。

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