β1- and β2-adrenoceptor responses in cardiomyocytes derived from human embryonic stem cells: comparison with failing and non-failing adult human heart
Article first published online: 29 JAN 2009
2008 British Pharmacological Society
British Journal of Pharmacology
Volume 153, Issue 4, pages 751–759, February 2008
How to Cite
Brito-Martins, M., Harding, S. E. and Ali, N. N. (2008), β1- and β2-adrenoceptor responses in cardiomyocytes derived from human embryonic stem cells: comparison with failing and non-failing adult human heart. British Journal of Pharmacology, 153: 751–759. doi: 10.1038/sj.bjp.0707619
- Issue published online: 29 JAN 2009
- Article first published online: 29 JAN 2009
- (Received July 20, 2007, Revised September 11, 2007, Accepted October 12, 2007)
- embryonic stem cell;
- beating rate
Background and purpose:
Characterization of human embryonic stem cell-derived cardiomyocytes (hESC-CM) in relation to adult myocytes is essential for their future use in transplantation or as a model system. The β-adrenoceptor pathways, which are known to be effective early in hESC-CM development, are of major importance because of their control of rate and force of beating, arrhythmia generation and apoptosis/necrosis. We have therefore performed detailed pharmacological analysis of the β-adrenoceptor responses in developing hESC-CM.
hESC-CMs were differentiated from H7 ESCs and studied up to 79 days of differentiation. Rate of beating and time course of contraction and relaxation were measured in superfused preparations.
Responses to the mixed β1- and β2-adrenoceptor agonist isoprenaline were evident from day 10 to day 79. Stability of the responses during an application, for repeated applications on the same experimental day and over the time of development, was determined. Concentrations for half-maximal response (12.9 nM) were similar to those from adult human heart, but closer to those obtained from failing rather than normal ventricle. Acceleration of both contraction and relaxation was quantitatively similar to that in adult ventricular myocytes, as was sensitivity to muscarinic inhibition. Use of specific antagonists showed that both β1- and β2-adrenoceptors contributed to contractile responses, as seen with adult myocytes.
Conclusions and implications:
These data show the compatibility of hESC-CM with adult human myocardium in terms of β-adrenoceptor response. The experiments described here also confirm the utility of the hESC-CM preparation for detailed pharmacological analysis.
British Journal of Pharmacology (2008) 153, 751–759; doi:10.1038/sj.bjp.0707619; published online 14 January 2008