Expression of the electrophysiological system during murine embryonic stem cell cardiac differentiation

Cell Physiol Biochem. 2003;13(5):263-70. doi: 10.1159/000074541.

Abstract

Background: Stem cell based replacement therapy is envisioned as a method to repair failing hearts suffering from cardiomyocyte loss. To prevent potentially lethal arrhythmias, the donor cellular electrophysiological make-up should match with the acceptor tissue. To engineer the desired electrophysiological phenotype, the underlying molecular regulation of ion channels and gap-junction proteins should be clarified first.

Methods: We established the expression of seven main cardiac ion channel a-subunits and four b-subunits using semiquantitive RT-PCR and two major cardiac gap-junction proteins by immunohistochemistry during the differentiation process of murine ES cells into cardiomyocytes.

Results: Ion channel mRNA expression profiles display sequential upregulation. Connexin-40 and -43 expression is low in early cardiomyocytes, increased expression rates were found in subsequent differentiation phases.

Conclusion: Cardiac differentiation of mouse embryonic stem cells is characterized by a sequential upregulation of the main cardiac ion channels and connexins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials
  • Animals
  • Base Sequence
  • Cell Differentiation
  • Connexin 43 / metabolism
  • Embryo, Mammalian / cytology*
  • Ion Channels / metabolism*
  • Mice
  • Molecular Sequence Data
  • Myocardium / metabolism
  • Myocytes, Cardiac / cytology
  • Myocytes, Cardiac / physiology*
  • Stem Cells / cytology*
  • Time Factors

Substances

  • Connexin 43
  • Ion Channels