Mesoangioblasts from ventricular vessels can differentiate in vitro into cardiac myocytes with sinoatrial-like properties

J Mol Cell Cardiol. 2010 Feb;48(2):415-23. doi: 10.1016/j.yjmcc.2009.10.006. Epub 2009 Oct 22.

Abstract

Cardiac mesoangioblasts (MABs) are a class of vessel-associated clonogenic, self-renewing progenitor cells, recently identified in the post-natal murine heart and committed to cardiac differentiation. Cardiomyocytes generated during cardiogenesis from progenitor cells acquire several distinct phenotypes, corresponding to different functional properties in diverse structures of the adult heart. Given the special functional relevance to rhythm generation and rate control of sinoatrial cells, and in view of their prospective use in therapeutical applications, we sought to determine if, and to what extent, cardiac mesoangioblasts could also differentiate into myocytes with properties typical of mature pacemaker myocytes. We report here that a subpopulation of cardiac mesoangioblasts, induced to differentiate in vitro into cardiomyocytes, do acquire a phenotype with specific mature pacemaker myocytes properties. These include expression of the HCN4 isoform of pacemaker ("funny", f-) channels and connexin 45 (Cx45), as well as reduced expression of inwardly-rectifying potassium channels. Furthermore, MAB-derived myocytes form agglomerates of pacing cells displaying stable rhythmic activity, and as in native cardiac pacemaker cells, f-channel modulation by autonomic transmitters contributes to control of spontaneous rate in differentiated mesoangioblasts. These data represent the first evidence for in vitro generation of pacemaker-like myocytes from proliferating non-embryonic stem/progenitor cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Blood Vessels / cytology*
  • Cell Differentiation*
  • Clone Cells
  • Cyclic Nucleotide-Gated Cation Channels / metabolism
  • GATA6 Transcription Factor / metabolism
  • Heart Ventricles / cytology*
  • Humans
  • Ion Channel Gating
  • Mice
  • Mice, Inbred C57BL
  • Myocytes, Cardiac / cytology*
  • Myocytes, Cardiac / metabolism
  • Protein Isoforms / metabolism
  • Receptors, Adrenergic, beta / metabolism
  • Receptors, Cholinergic / metabolism
  • Sinoatrial Node / cytology*
  • Stem Cells / cytology*
  • Stem Cells / metabolism

Substances

  • Biomarkers
  • Cyclic Nucleotide-Gated Cation Channels
  • GATA6 Transcription Factor
  • Protein Isoforms
  • Receptors, Adrenergic, beta
  • Receptors, Cholinergic