Electrophysiological integration and action potential properties of transplanted cardiomyocytes derived from induced pluripotent stem cells

Cardiovasc Res. 2013 Dec 1;100(3):432-40. doi: 10.1093/cvr/cvt213. Epub 2013 Sep 16.

Abstract

Aims: Induced pluripotent stem cell-derived cardiomyocytes (iPSCM) are regarded as promising cell type for cardiac cell replacement therapy. We investigated long-term electrophysiological integration and maturation of transplanted iPSCM, which are essential for therapeutic benefit.

Methods and results: Murine iPSCM expressing enhanced green fluorescent protein and a puromycin resistance under control of the α-myosin heavy chain promoter were purified by antibiotic selection and injected into adult mouse hearts. After 6-12 days, 3-6 weeks, or 6-8 months, viable slices of recipient hearts were prepared. Slices were focally stimulated by a unipolar electrode placed in host tissue, and intracellular action potentials (APs) were recorded with glass microelectrodes in transplanted cells and neighbouring host tissue within the slices. Persistence and electrical integration of transplanted iPSCM into recipient hearts could be demonstrated at all time points. Quality of coupling improved, as indicated by a maximal stimulation frequency without conduction blocks of 5.77 ± 0.54 Hz at 6-12 days, 8.98 ± 0.38 Hz at 3-6 weeks and 10.82 ± 1.07 Hz at 6-8 months after transplantation. AP properties of iPSCM became more mature from 6-12 days to 6-8 months after transplantation, but still differed significantly from those of host APs.

Conclusion: Transplanted iPSCM can persist in the long term and integrate electrically into host tissue, supporting their potential for cell replacement therapy. Quality of electrical integration improves between 6-12 days and 6-8 months after transplantation, and there are signs of an electrophysiological maturation. However, even after 6-8 months, AP properties of transplanted iPSCM differ from those of recipient cardiomyocytes.

Keywords: Conduction; Electrophysiology; Transplantation; iPSCM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials
  • Animals
  • Cell Differentiation*
  • Cell Line
  • Cell Survival
  • Green Fluorescent Proteins / biosynthesis
  • Green Fluorescent Proteins / genetics
  • Induced Pluripotent Stem Cells / metabolism
  • Induced Pluripotent Stem Cells / transplantation*
  • Male
  • Mice
  • Mice, 129 Strain
  • Mice, Inbred C57BL
  • Myocytes, Cardiac / metabolism
  • Myocytes, Cardiac / transplantation*
  • Myosin Heavy Chains / genetics
  • Promoter Regions, Genetic
  • Time Factors
  • Transfection
  • Ventricular Myosins / genetics

Substances

  • enhanced green fluorescent protein
  • Green Fluorescent Proteins
  • Ventricular Myosins
  • Myosin Heavy Chains