1. Academic Validation
  2. Simple Workflow and Comparison of Media for hPSC-Cardiomyocyte Cryopreservation and Recovery

Simple Workflow and Comparison of Media for hPSC-Cardiomyocyte Cryopreservation and Recovery

  • Curr Protoc Stem Cell Biol. 2020 Dec;55(1):e125. doi: 10.1002/cpsc.125.
Duncan C Miller 1 2 Carolin Genehr 1 Narasimha S Telugu 1 Silke Kurths 1 Sebastian Diecke 1 2 3
Affiliations

Affiliations

  • 1 Core Facility Stem Cells, Max-Delbrück-Centrum, Berlin, Germany.
  • 2 DZHK (German Centre for Cardiovascular Research), partner site Berlin, Berlin, Germany.
  • 3 Berlin Institute of Health (BIH), Berlin, Germany.
Abstract

Great progress has been made with protocols for the differentiation and functional application of hPSC-cardiomyocytes (hPSC-CMs) in recent years; however, the cryopreservation and recovery of hPSC-CMs still presents challenges and few reports describe in detail the protocols and general workflow. In order to facilitate cryopreservation and recovery of hPSC-CMs for a wide range of applications, we provide detailed information and step-by-step protocols. The protocols are simple and use common reagents. They are comprised of a fast dissociation, cryopreservation using standard equipment, and gentle recovery following thawing. We discuss various features of the protocols, as well as their utilization in the context of common hPSC-CM differentiation and application workflows. Finally, we compare two proprietary and two common in-house formulations of cryopreservation media used for hPSC-CMs, and despite differences in their price and composition find broadly similar recovery rates and cellular function after thawing. © 2019 The Authors. Basic Protocol 1: Dissociation and cryopreservation of hPSC-CMs Basic Protocol 2: Thawing and recovery of cryogenically frozen hPSC-CMs.

Keywords

cardiomyocytes; cryopreservation; freezing media; functional recovery; human pluripotent stem cells.

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