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三维胶原蛋白凝胶中的微结构材料与机械信号

Micro-structured materials and mechanical cues in 3D collagen gels.

作者信息

Phillips James B, Brown Robert

机构信息

Department of Life Sciences, The Open University, Milton Keynes, UK.

出版信息

Methods Mol Biol. 2011;695:183-96. doi: 10.1007/978-1-60761-984-0_12.

Abstract

Collagen gels provide a versatile and widely used substrate for three-dimensional (3D) cell culture. Here we describe how cell-seeded Type-I collagen gels can be adapted to provide powerful 3D models to support a wide range of research applications where cell/substrate alignment, density, stiffness/compliance, and strain are critical factors. In their fully hydrated form, rectangular collagen gels can be tethered such that endogenous forces generated as resident cells attach to and remodel the fibrillar collagen network can align the substrate in a controllable, predictable, and quantifiable manner. By removing water from collagen gels (plastic compression), their density increases towards that of body tissues, facilitating the engineering of a range of biomimetic constructs with controllable mechanical properties. This dense collagen can be used in combination with other components to achieve a range of functional properties from controlled perfusion, or tensile/compressive strength to new micro-structures. Detailed methodology is provided for the assembly of a range of 3D collagen materials including tethered aligned hydrogels and plastic compressed constructs. A range of techniques for analysing cell behaviour within these models, including microscopy and molecular analyses are described. These systems therefore provide a highly controllable mechanical and chemical micro-environment for investigating a wide range of cellular responses.

摘要

胶原蛋白凝胶为三维(3D)细胞培养提供了一种通用且广泛使用的基质。在此,我们描述了如何对接种细胞的I型胶原蛋白凝胶进行改造,以提供强大的3D模型,来支持一系列研究应用,其中细胞/基质排列、密度、硬度/顺应性和应变是关键因素。在完全水合状态下,矩形胶原蛋白凝胶可以被束缚,使得驻留细胞附着并重塑纤维状胶原蛋白网络时产生的内力能够以可控、可预测和可量化的方式使基质排列。通过从胶原蛋白凝胶中去除水分(塑性压缩),其密度向身体组织的密度增加,有助于构建一系列具有可控机械性能的仿生构建体。这种致密的胶原蛋白可与其他成分结合使用,以实现从可控灌注、拉伸/压缩强度到新的微观结构等一系列功能特性。本文提供了一系列3D胶原蛋白材料组装的详细方法,包括束缚排列的水凝胶和塑性压缩构建体。还描述了一系列用于分析这些模型内细胞行为的技术,包括显微镜检查和分子分析。因此,这些系统为研究广泛的细胞反应提供了高度可控的机械和化学微环境。

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