Micro-arrayed human embryonic stem cells-derived cardiomyocytes for in vitro functional assay

PLoS One. 2012;7(11):e48483. doi: 10.1371/journal.pone.0048483. Epub 2012 Nov 12.

Abstract

Introduction: The heart is one of the least regenerative organs in the body and any major insult can result in a significant loss of heart cells. The development of an in vitro-based cardiac tissue could be of paramount importance for many aspects of the cardiology research. In this context, we developed an in vitro assay based on human cardiomyocytes (hCMs) and ad hoc micro-technologies, suitable for several applications: from pharmacological analysis to physio-phatological studies on transplantable hCMs. We focused on the development of an assay able to analyze not only hCMs viability, but also their functionality.

Methods: hCMs were cultured onto a poly-acrylamide hydrogel with tunable tissue-like mechanical properties and organized through micropatterning in a 20×20 array. Arrayed hCMs were characterized by immunofluorescence, GAP-FRAP analyses and live and dead assay. Their functionality was evaluated monitoring the excitation-contraction coupling.

Results: Micropatterned hCMs maintained the expression of the major cardiac markers (cTnT, cTnI, Cx43, Nkx2.5, α-actinin) and functional properties. The spontaneous contraction frequency was (0.83±0.2) Hz, while exogenous electrical stimulation lead to an increase up to 2 Hz. As proof of concept that our device can be used for screening the effects of pathological conditions, hCMs were exposed to increasing levels of H(2)O(2). Remarkably, hCMs viability was not compromised with exposure to 0.1 mM H(2)O(2), but hCMs contractility was dramatically suppressed. As proof of concept, we also developed a microfluidic platform to selectively treat areas of the cell array, in the perspective of performing multi-parametric assay.

Conclusions: Such system could be a useful tool for testing the effects of multiple conditions on an in vitro cell model representative of human heart physiology, thus potentially helping the processes of therapy and drug development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Culture Techniques
  • Cell Differentiation
  • Cell Line
  • Embryonic Stem Cells / cytology*
  • Gene Expression Profiling*
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Myocardial Contraction / drug effects
  • Myocytes, Cardiac / cytology*
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism*
  • Oligonucleotide Array Sequence Analysis*
  • Oxidative Stress / genetics

Substances

  • Hydrogen Peroxide

Grants and funding

This work was supported by Progetti Di Eccellenza Ca.Ri.Pa.Ro, Fondo Sociale Europeo (grant code 2105/1/10/1268/2008) and the Università degli Studi di Padova. ES and EC were supported by “Fondo Sociale Europeo”, ES and TZ by the Progetto Giovani Studiosi 2010, University of Padova. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.