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用于高通量分析细胞-细胞外基质相互作用的多孔组合水凝胶阵列。

Multiwell Combinatorial Hydrogel Array for High-Throughput Analysis of Cell-ECM Interactions.

机构信息

Department of Chemistry, Latimer Hall, University of California, Berkeley, Berkeley, California 94720, United States.

Department of Bioengineering, Stanley Hall, University of California, Berkeley, Berkeley, California 94720, United States.

出版信息

ACS Biomater Sci Eng. 2021 Jun 14;7(6):2453-2465. doi: 10.1021/acsbiomaterials.1c00065. Epub 2021 May 24.

Abstract

Biophysical cues in the extracellular matrix (ECM) regulate cell behavior in a complex, nonlinear, and interdependent manner. To quantify these important regulatory relationships and gain a comprehensive understanding of mechanotransduction, there is a need for high-throughput matrix platforms that enable parallel culture and analysis of cells in various matrix conditions. Here we describe a multiwell hyaluronic acid (HA) platform in which cells are cultured on combinatorial arrays of hydrogels spanning a range of elasticities and adhesivities. Our strategy utilizes orthogonal photopatterning of stiffness and adhesivity gradients, with the stiffness gradient implemented by a programmable light illumination system. The resulting platform allows individual treatment and analysis of each matrix environment while eliminating contributions of haptotaxis and durotaxis. In human mesenchymal stem cells, our platform recapitulates expected relationships between matrix stiffness, adhesivity, and cell mechanosensing. We further applied the platform to show that as integrin ligand density falls, cell adhesion and migration depend more strongly on CD44-mediated interactions with the HA backbone. We anticipate that our system could bear great value for mechanistic discovery and screening where matrix mechanics and adhesivity are expected to influence phenotype.

摘要

细胞外基质(ECM)中的生物物理线索以复杂、非线性和相互依存的方式调节细胞行为。为了量化这些重要的调节关系并全面了解机械转导,需要有高通量的基质平台,能够平行培养和分析各种基质条件下的细胞。在这里,我们描述了一种多孔透明质酸(HA)平台,其中细胞在跨越一系列弹性和粘附性的水凝胶组合阵列上培养。我们的策略利用刚度和粘附性梯度的正交光图案化,通过可编程的光照系统实现刚度梯度。该平台允许单独处理和分析每个基质环境,同时消除趋触性和趋硬性的影响。在人骨髓间充质干细胞中,我们的平台再现了基质刚度、粘附性和细胞机械感知之间的预期关系。我们进一步应用该平台表明,随着整合素配体密度的降低,细胞黏附和迁移越来越依赖于与 HA 主链的 CD44 介导的相互作用。我们预计,我们的系统在需要考虑基质力学和粘附性可能影响表型的机械发现和筛选中具有很大的价值。

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