Non-Invasive Acoustical sensing of Drug-Induced Effects on the Contractile Machinery of Human Cardiomyocyte Clusters

PLoS One. 2015 May 11;10(5):e0125540. doi: 10.1371/journal.pone.0125540. eCollection 2015.

Abstract

There is an urgent need for improved models for cardiotoxicity testing. Here we propose acoustic sensing applied to beating human cardiomyocyte clusters for non-invasive, surrogate measuring of the QT interval and other characteristics of the contractile machinery. In experiments with the acoustic method quartz crystal microbalance with dissipation monitoring (QCM-D), the shape of the recorded signals was very similar to the extracellular field potential detected in electrochemical experiments, and the expected changes of the QT interval in response to addition of conventional drugs (E-4031 or nifedipine) were observed. Additionally, changes in the dissipation signal upon addition of cytochalasin D were in good agreement with the known, corresponding shortening of the contraction-relaxation time. These findings suggest that QCM-D has great potential as a tool for cardiotoxicological screening, where effects of compounds on the cardiomyocyte contractile machinery can be detected independently of whether the extracellular field potential is altered or not.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biosensing Techniques / methods
  • Cell Line
  • Cytochalasin D / pharmacology
  • Humans
  • Isoproterenol / pharmacology
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism*
  • Nifedipine
  • Piperidines / pharmacology
  • Pyridines / pharmacology
  • Quartz Crystal Microbalance Techniques

Substances

  • Piperidines
  • Pyridines
  • E 4031
  • Cytochalasin D
  • Nifedipine
  • Isoproterenol

Grants and funding

Support was provided to the following authors: SS: Kristina Stenborgs stiftelse; Swedish Research Council (VR) through the Linneaus program SUPRA [2007-125] and grant no 2012-4217; PS: the Systems Biology Research Centre (University of Skövde, Sweden) under grants from the Knowledge Foundation [2011/0295 and 2013/89]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Co-authors Daniella Steel, Kerstin Dahlenborg and Peter Sartipy were employed by Cellectis AB. Cellectis AB provided support in the form of salaries for authors DS, KD and PS, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘author contributions’ section. Co-author Sofia Svedhem was part time employed by Biolin Scientific/Q-Sense. Biolin Scientific/Q-Sense provided application support, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.