Literature DB >> 34582849

Droplet-based vitrification of adherent human induced pluripotent stem cells on alginate microcarrier influenced by adhesion time and matrix elasticity.

Ina Meiser1, Julia Majer2, Alisa Katsen-Globa2, André Schulz2, Katharina Schmidt2, Frank Stracke2, Eirini Koutsouraki3, Gesa Witt4, Oliver Keminer4, Ole Pless4, John Gardner3, Carsten Claussen4, Philip Gribbon4, Julia C Neubauer5, Heiko Zimmermann6.   

Abstract

The gold standard in cryopreservation is still conventional slow freezing of single cells or small aggregates in suspension, although major cell loss and limitation to non-specialised cell types in stem cell technology are known drawbacks. The requirement for rapidly available therapeutic and diagnostic cell types is increasing constantly. In the case of human induced pluripotent stem cells (hiPSCs) or their derivates, more sophisticated cryopreservation protocols are needed to address this demand. These should allow a preservation in their physiological, adherent state, an efficient re-cultivation and upscaling upon thawing towards high-throughput applications in cell therapies or disease modelling in drug discovery. Here, we present a novel vitrification-based method for adherent hiPSCs, designed for automated handling by microfluidic approaches and with ready-to-use potential e.g. in suspension-based bioreactors after thawing. Modifiable alginate microcarriers serve as a growth surface for adherent hiPSCs that were cultured in a suspension-based bioreactor and subsequently cryopreserved via droplet-based vitrification in comparison to conventional slow freezing. Soft (0.35%) versus stiff (0.65%) alginate microcarriers in concert with adhesion time variation have been examined. Findings revealed specific optimal conditions leading to an adhesion time and growth surface (matrix) elasticity dependent hypothesis on cryo-induced damaging regimes for adherent cell types. Deviations from the found optimum parameters give rise to membrane ruptures assessed via SEM and major cell loss after adherent vitrification. Applying the optimal conditions, droplet-based vitrification was superior to conventional slow freezing. A decreased microcarrier stiffness was found to outperform stiffer material regarding cell recovery, whereas the stemness characteristics of rewarmed hiPSCs were preserved.
Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

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Keywords:  Adherent cryopreservation; Human induced pluripotent stem cells; Microcarrier; Vitrification

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Year:  2021        PMID: 34582849     DOI: 10.1016/j.cryobiol.2021.09.010

Source DB:  PubMed          Journal:  Cryobiology        ISSN: 0011-2240            Impact factor:   2.487


  1 in total

1.  Standardization of Cell Culture Conditions and Routine Genomic Screening under a Quality Management System Leads to Reduced Genomic Instability in hPSCs.

Authors:  Francisco J Molina-Ruiz; Clelia Introna; Georgina Bombau; Mireia Galofre; Josep M Canals
Journal:  Cells       Date:  2022-06-21       Impact factor: 7.666

  1 in total

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