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一种用于自组装软生物材料原位单轴测试的新方法。

A novel technique for in situ uniaxial tests of self-assembled soft biomaterials.

机构信息

University of Illinois at Urbana-Champaign, 1206 W. Green St, Urbana, IL 61801, USA.

出版信息

Lab Chip. 2019 Mar 27;19(7):1153-1161. doi: 10.1039/c8lc01273c.

Abstract

We introduce a novel method to form 3D biomimetic tissues from a droplet of a cell-extracellular matrix (ECM) mixture on a sensor stage and to quantify tissue force and stiffness as a function of time under optical microscopes. This method exploits advances in micro-nano fabrication and capillarity for self-assembly and self-alignment of tissues on the stage. It allows simultaneous investigation of the microstructure of the tissue in situ while its mechanical response is quantified, thus linking tissue biophysics with physiology and revealing structural-functional properties of 3D tissues. We demonstrate the functionality of the stage by studying the mechanical behavior of different cell-collagen mixtures under mechanical, chemical and electrical stimulation. This includes force evolution in cell-free collagen during curing, myotubes differentiated from muscle cell-collagen/Matrigel ECM subjected to electrical stimulation, and fibroblast-collagen tissue subjected to cancer cell conditioned media (CM) and a Rho-kinase inhibitor, Y27632. Muscle contraction decreases with increasing frequency of electrical stimulation, and fibroblasts respond to CM by increasing contractility for a short time and completely relax in the presence of Y27632 but restore force with Y27632 washout.

摘要

我们介绍了一种新方法,可将细胞-细胞外基质(ECM)混合物的液滴在传感器平台上形成 3D 仿生组织,并在光学显微镜下定量研究组织力和刚度随时间的变化。该方法利用微纳制造和毛细作用的进展,实现了组织在平台上的自组装和自对准。它允许在原位研究组织的微观结构的同时对其机械响应进行定量分析,从而将组织生物物理学与生理学联系起来,并揭示 3D 组织的结构功能特性。我们通过研究不同细胞-胶原蛋白混合物在机械、化学和电刺激下的力学行为来验证该平台的功能。这包括在胶原蛋白固化过程中细胞游离胶原蛋白的力演化、受电刺激的肌细胞-胶原蛋白/基质胶 ECM 分化的肌管,以及受癌细胞条件培养基(CM)和 Rho 激酶抑制剂 Y27632 影响的成纤维细胞-胶原蛋白组织。肌肉收缩随电刺激频率的增加而减少,而成纤维细胞对 CM 的反应是在短时间内增加收缩力,在 Y27632 存在下完全松弛,但在 Y27632 冲洗后恢复力。

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