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A review of protocols for human iPSC culture, cardiac differentiation, subtype-specification, maturation, and direct reprogramming

Journal

STAR PROTOCOLS
Volume 3, Issue 3, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.xpro.2022.101560

Keywords

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Funding

  1. NIH [CA220002, CA261898, R01 HL153220]
  2. American Heart Association Postdoctoral Fellowship [874276]
  3. German Federal Ministry of Education and Research (BMBF)/German Center for Cardiovascular Research (DZHK)
  4. German Research Foundation (DFG) [EXC 2067/1-390729940, CY 90/1-1, SFB1002 S01]
  5. Else-Kroner-Fersenius Foundation [2019_A75]

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This article discusses the evolution of culture and cardiomyocyte differentiation methods for human embryonic stem cells and human induced pluripotent stem cells (hiPSC), as well as the importance of using these cells in human disease modeling and drug discovery.
The methods for the culture and cardiomyocyte differentiation of human embryonic stem cells, and later human induced pluripotent stem cells (hiPSC), have moved from a complex and uncontrolled systems to simplified and relatively robust protocols, using the knowledge and cues gathered at each step. HiPSCderived cardiomyocytes have proven to be a useful tool in human disease modelling, drug discovery, developmental biology, and regenerative medicine. In this protocol review, we will highlight the evolution of protocols associated with hPSC culture, cardiomyocyte differentiation, sub-type specification, and cardiomyocyte maturation. We also discuss protocols for somatic cell direct reprogramming to cardiomyocyte-like cells.

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