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Cancer Cell death Cell cycle Cytoskeleton Exo/endocytosis Differentiation Division Organelles Signalling Stem cells Trafficking
Editor-in-Chief
DN Wheatley
(Aberdeen, U.K.)
Co-Editors
Susan R. McGlashan
(Auckland, New Zealand)
Sidney S. Yu
(Shatin, Hong Kong)
Regional Editors
H Carvalho
(Campinas, Brazil)
H Chang Chan
(Shatin, Hong Kong)
C Green
(Auckland, New Zealand)
S Kidson
(Cape Town, South Africa)
E Nadezhdina
(Moscow, Russia)
G Sluder
(Worcester, U.S.A.)
Managing Editor
AJ Panther
(Aberdeen, U.K.)
Cell Biology International (2009) Immediate Publication, doi:10.1042/CBI20090021
Controlling the in vitro differentiation of embryonic stem cells for myocardial tissue engineering applications
Dong-Bo Ou, Rui Chen, Xiong-Tao Liu, Jing-Jing Guo, Hong-Tao Wang and Qiang-Sun Zheng
Department of Cardiology and Arrhythmologic Centre, Tangdu Hospital, Xi’an, China. tdxnsys@fmmu.edu.cn


We studied the differentiation of embryonic stem cells (ESCs) and developed a novel protocol for generating functional cardiomyocytes (CMs) from ESCs by co-culturing these with live cardiac cells. We then evaluated the structural and functional properties of these ESC-derived CMs (ESCMs). An acellular matrix obtained from rabbit heart tissues was used as a scaffold. Then ESCMs were seeded onto the acellular matrix for preliminary tissue engineering applications. We found that by mimicking the cardiac microenvironment, the percentage of beating embryoid bodies (EBs) was much higher and the homogeneity of EBs were significantly improved over that seen in the control group (p<0.001). ESCMs in EBs acquired almost the same structural and functional properties as typical CMs. After implantation, the cells in the EBs rapidly grew and expanded in the extracellular matrix. These results indicate that the differentiation of ESCs can be controlled in a cardiac mimicking microenvironment and that ESCs can be used as an ideal cell source for large-scale tissue engineering applications for the procurement of cardiac muscle.
doi:10.1042/CBI20090021
Received 1 June 2009/20 August 2009; Accepted 15 September 2009
Published as Immediate Publication 15 September 2009

ISSN Print: 1065-6995
ISSN Electronic: 1095-8355
Published by Portland Press Limited on behalf of the International Federation for Cell Biology (IFCB)