4.6 Article

Maturation of Pluripotent Stem Cell-Derived Cardiomyocytes Enables Modeling of Human Hypertrophic Cardiomyopathy

Journal

STEM CELL REPORTS
Volume 16, Issue 3, Pages 519-533

Publisher

CELL PRESS
DOI: 10.1016/j.stemcr.2021.01.018

Keywords

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Funding

  1. University of Colorado Consortium for Fibrosis Research Translation
  2. NIH Cardiology training grant [T32HL007822]
  3. American Heart Association postdoctoral fellowship [19POST34380250]
  4. NIH/CCTSI CO-Pilot Mentored Faculty Award
  5. Boettcher Foundation
  6. American Heart Association
  7. University of Colorado Department of Medicine Outstanding Early Career Scholar Program
  8. Gates Frontiers Fund
  9. NIH [HL133230, HL150225, HL127240, DK119594, HL116848]
  10. American Heart Association [16POST30960017, 16SFRN31400013]

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Researchers developed a method to drive cultured hiPSC-CMs towards maturity, resulting in cells with characteristics of adult human cardiomyocytes. These mature hiPSC-CMs could serve as a useful in vitro platform for studying and characterizing cardiovascular diseases.
Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) are a powerful platform for biomedical research. However, they are immature, which is a barrier to modeling adult-onset cardiovascular disease. Here, we sought to develop a simple method that could drive cultured hiPSC-CMs toward maturity across a number of phenotypes, with the aim of utilizing mature hiPSC-CMs to model human cardiovascular disease. hiPSC-CMs were cultured in fatty acid-based medium and plated on micropatterned surfaces. These cells display many characteristics of adult human cardiomyocytes, including elongated cell morphology, sarcomeric maturity, and increased myofibril contractile force. In addition, mature hiPSC-CMs develop pathological hypertrophy, with associated myofibril relaxation defects, in response to either a pro-hypertrophic agent or genetic mutations. The more mature hiPSC-CMs produced by these methods could serve as a useful in vitro platform for characterizing cardiovascular disease.

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