4.8 Article

Mechanotransduction of human pluripotent stem cells cultivated on tunable cell-derived extracellular matrix

Journal

BIOMATERIALS
Volume 150, Issue -, Pages 100-111

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2017.10.016

Keywords

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Funding

  1. National Research Foundation of Korea (NRF) from Ministry of Science, ICT and Future Planning [2015R1A2A2A04004469, 2015-M3A9C7030091]
  2. Ministry of Agriculture, Food and Rural Affairs, Republic of Korea [715003071HD120]
  3. Institute of Planning & Evaluation for Technology in Food, Agriculture, Forestry & Fisheries (iPET), Republic of Korea [715003071HD120] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  4. National Research Foundation of Korea [2015R1A2A2A04004469, 21A20132200012] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Cell-derived matrices (CDM) are becoming an attractive alternative to conventional biological scaffolding platforms due to its unique ability to closely recapitulate a native extracellular matrix (ECM) de novo. Although cell-substrate interactions are recognized to be principal in regulating stem cell behavior, very few studies have documented the acclimation of human pluripotent stem cells (hPSCs) on pristine and altered cell-derived matrices. Here, we investigate crosslink-induced mechanotransduction of hPSCs cultivated on decellularized fibroblast-derived matrices (FDM) to explore cell, adhesion, growth, migration, and pluripotency in various biological landscapes. The results showed either substrate-mediated induction or inhibition of the Epithelial-Mesenchymal-Transition (EMT) program, strongly suggesting that FDM stiffness can be a dominant factor in mediating hPSC plasticity. We further propose an optimal FDM substratum intended for long-term hPSC cultivation in a feeder-free niche-like microenvironment. This study carries significant implications for hPSC cultivation and encourages more in-depth studies towards the fundamentals of hPSC-CDM interactions. (C) 2017 Elsevier Ltd. All rights reserved.

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