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A platform for assessing chemotactic migration within a spatiotemporally defined 3D microenvironment

机译:评估时空定义的3D微环境中趋化迁移的平台

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摘要

While the quantification of cell movement within defined biochemical gradients is now possible with microfluidic approaches, translating this capability to biologically relevant three-dimensional microenvironments remains a challenge. We introduce an accessible platform, requiring only standard tools (e.g. pipettes), that provides robust soluble factor control within a three-dimensional biological matrix. We demonstrate long-lasting linear and non-linear concentration profiles that were maintained for up to ten days using 34.5 μL solute volume. We also demonstrate the ability to superimpose local soluble factor pulses onto existing gradients via defined dosing windows. The combination of long-term and transient gradient characteristics within a three-dimensional environment opens the door for signaling studies that investigate the migratory behavior of cells within a biologically representative matrix. To this end, we apply temporally evolving and long-lasting gradients to study the chemotactic responses of human neutrophils and the invasion of metastatic rat mammary adenocarcinoma cells (MtLN3) within three-dimensional collagen matrices.
机译:虽然现在可以通过微流控方法对确定的生化梯度内的细胞运动进行定量,但将这种能力转化为生物学相关的三维微环境仍然是一个挑战。我们引入了一个可访问的平台,该平台仅需要标准工具(例如移液器),即可在三维生物矩阵中提供强大的可溶性因子控制。我们证明了使用34.5μL溶质体积可以维持长达十天的线性和非线性浓度曲线。我们还展示了通过定义的剂量窗口将局部可溶因子脉冲叠加到现有梯度上的能力。三维环境中长期和瞬态梯度特征的组合为研究生物学上具有代表性的基质中细胞的迁移行为的信号研究打开了大门。为此,我们应用时间演变和持久的梯度来研究人类中性粒细胞的趋化反应以及三维胶原蛋白基质中转移性大鼠乳腺腺癌细胞(MtLN3)的侵袭。

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