3.8 Article

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

Journal

ACS BIOMATERIALS SCIENCE & ENGINEERING
Volume 7, Issue 6, Pages 2453-2465

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsbiomaterials.1c00065

Keywords

mechanobiology; biomaterials; hyaluronic acid; combinatorial matrix arrays

Funding

  1. National Institutes of Health [R01GM122375, R01CA227136, R01CA260443, R01NS074831, R01DK118940]
  2. National Science Foundation

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Biophysical cues in the extracellular matrix regulate cell behavior in a complex, nonlinear, and interdependent manner. A high-throughput HA platform has been developed for parallel culture and analysis of cells in various matrix conditions. This platform allows individual treatment and analysis of each matrix environment, providing valuable insights into mechanotransduction.
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.

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