4.7 Review

Subtype-specific cardiomyocytes for precision medicine: Where are we now?

Journal

STEM CELLS
Volume 38, Issue 7, Pages 822-833

Publisher

OXFORD UNIV PRESS
DOI: 10.1002/stem.3178

Keywords

atrial cardiomyocytes; human pluripotent stem cells; nodal cardiomyocytes; subtype-specific cardiomyocytes; ventricular cardiomyocytes

Funding

  1. American Heart Association (AHA) Career Development Awards [18CDA34110293, 18CDA34110352]
  2. National Institute of Health (NIH) [R01 HL121797, R01 HL144009, R01HL132801]
  3. Abigail Wexner Research Institute at Nationwide Children's Hospital

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Patient-derived pluripotent stem cells (PSCs) have greatly transformed the current understanding of human heart development and cardiovascular disease. Cardiomyocytes derived from personalized PSCs are powerful tools for modeling heart disease and performing patient-based cardiac toxicity testing. However, these PSC-derived cardiomyocytes (PSC-CMs) are a mixed population of atrial-, ventricular-, and pacemaker-like cells in the dish, hindering the future of precision cardiovascular medicine. Recent insights gleaned from the developing heart have paved new avenues to refine subtype-specific cardiomyocytes from patients with known pathogenic genetic variants and clinical phenotypes. Here, we discuss the recent progress on generating subtype-specific (atrial, ventricular, and nodal) cardiomyocytes from the perspectives of embryonic heart development, and how they will expand our current knowledge on molecular mechanisms of cardiovascular disease and the future of precision medicine.

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