Modeling Cardiovascular Diseases with Patient-Specific Human Pluripotent Stem Cell-Derived Cardiomyocytes

Methods Mol Biol. 2016:1353:119-30. doi: 10.1007/7651_2015_196.

Abstract

The generation of cardiomyocytes from human induced pluripotent stem cells (hiPSCs) provides a source of cells that accurately recapitulate the human cardiac pathophysiology. The application of these cells allows for modeling of cardiovascular diseases, providing a novel understanding of human disease mechanisms and assessment of therapies. Here, we describe a stepwise protocol developed in our laboratory for the generation of hiPSCs from patients with a specific disease phenotype, long-term hiPSC culture and cryopreservation, differentiation of hiPSCs to cardiomyocytes, and assessment of disease phenotypes. Our protocol combines a number of innovative tools that include a codon-optimized mini intronic plasmid (CoMiP), chemically defined culture conditions to achieve high efficiencies of reprogramming and differentiation, and calcium imaging for assessment of cardiomyocyte phenotypes. Thus, this protocol provides a complete guide to use a patient cohort on a testable cardiomyocyte platform for pharmacological drug assessment.

Keywords: Calcium imaging; Cardiomyocytes; Disease modeling; Human induced pluripotent stem cells.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Antigens, Surface / genetics
  • Antigens, Surface / metabolism
  • Biomarkers / metabolism
  • Calcium / metabolism
  • Cardiomyopathy, Dilated / genetics
  • Cardiomyopathy, Dilated / metabolism
  • Cardiomyopathy, Dilated / pathology*
  • Cell Differentiation
  • Cellular Reprogramming*
  • Cryopreservation
  • Dermis / cytology
  • Dermis / metabolism
  • Fibroblasts / cytology*
  • Fibroblasts / metabolism
  • Gene Expression
  • Humans
  • Induced Pluripotent Stem Cells / cytology*
  • Induced Pluripotent Stem Cells / drug effects
  • Induced Pluripotent Stem Cells / metabolism
  • Intercellular Signaling Peptides and Proteins / pharmacology
  • Models, Biological*
  • Molecular Imaging
  • Mutation
  • Myocytes, Cardiac / cytology*
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism
  • Plasmids / chemistry
  • Plasmids / metabolism
  • Primary Cell Culture
  • Proteoglycans / genetics
  • Proteoglycans / metabolism
  • SOXB1 Transcription Factors / genetics
  • SOXB1 Transcription Factors / metabolism
  • Serial Passage
  • Troponin T / genetics
  • Troponin T / metabolism

Substances

  • Antigens, Surface
  • Biomarkers
  • Intercellular Signaling Peptides and Proteins
  • Proteoglycans
  • SOX2 protein, human
  • SOXB1 Transcription Factors
  • TNNT2 protein, human
  • TRA-1-60 antigen, human
  • Troponin T
  • Calcium