TY - JOUR
T1 - Comparison of contractile behavior of native murine ventricular tissue and cardiomyocytes derived from embryonic or induced pluripotent stem cells
AU - Xi, Jiaoya
AU - Khalil, Markus
AU - Shishechian, Nava
AU - Hannes, Tobias
AU - Pfannkuche, Kurt
AU - Liang, Huamin
AU - Fatima, Azra
AU - Haustein, Moritz
AU - Suhr, Frank
AU - Bloch, Wilhelm
AU - Reppel, Michael
AU - Sarić, Tomo
AU - Wernig, Marius
AU - Jänisch, Rudolf
AU - Brockmeier, Konrad
AU - Hescheler, Jürgen
AU - Pillekamp, Frank
PY - 2010/8/1
Y1 - 2010/8/1
N2 - Cardiomyocytes generated from embryonic stem cells (ESCs) and induced pluripotent stem (iPS) cells are suggested for repopulation of destroyed myocardium. Because contractile properties are crucial for functional regeneration, we compared cardiomyocytes differentiated from ES cells (ESC-CMs) and iPS cells (iPS-CMs). Native myocardium served as control. Murine ESCs or iPS cells were differentiated 11 d in vitro and cocultured 5-7 d with irreversibly injured myocardial tissue slices. Vital embryonic ventricular tissue slices of similar age served for comparison. Force-frequency relationship (FFR), effects of Ca(2+), Ni(2+), nifedipine, ryanodine, beta-adrenergic, and muscarinic modulation were studied during loaded contractions. FFR was negative for ESC-CMs and iPS-CMs. FFR was positive for embryonic tissue and turned negative after treatment with ryanodine. In all groups, force of contraction and relaxation time increased with the concentration of Ca(2+) and decreased with nifedipine. Force was reduced by Ni(2+). Isoproterenol (1 microM) increased the force most pronounced in embryonic tissue (207+/-31%, n=7; ESC-CMs: 123+/-5%, n=4; iPS-CMs: 120+/-4%, n=8). EC(50) values were similar. Contractile properties of iPS-CMs and ESC-CMs were similar, but they were significantly different from ventricular tissue of comparable age. The results indicate immaturity of the sarcoplasmic reticulum and the beta-adrenergic response of iPS-CMs and ESC-CMs.
AB - Cardiomyocytes generated from embryonic stem cells (ESCs) and induced pluripotent stem (iPS) cells are suggested for repopulation of destroyed myocardium. Because contractile properties are crucial for functional regeneration, we compared cardiomyocytes differentiated from ES cells (ESC-CMs) and iPS cells (iPS-CMs). Native myocardium served as control. Murine ESCs or iPS cells were differentiated 11 d in vitro and cocultured 5-7 d with irreversibly injured myocardial tissue slices. Vital embryonic ventricular tissue slices of similar age served for comparison. Force-frequency relationship (FFR), effects of Ca(2+), Ni(2+), nifedipine, ryanodine, beta-adrenergic, and muscarinic modulation were studied during loaded contractions. FFR was negative for ESC-CMs and iPS-CMs. FFR was positive for embryonic tissue and turned negative after treatment with ryanodine. In all groups, force of contraction and relaxation time increased with the concentration of Ca(2+) and decreased with nifedipine. Force was reduced by Ni(2+). Isoproterenol (1 microM) increased the force most pronounced in embryonic tissue (207+/-31%, n=7; ESC-CMs: 123+/-5%, n=4; iPS-CMs: 120+/-4%, n=8). EC(50) values were similar. Contractile properties of iPS-CMs and ESC-CMs were similar, but they were significantly different from ventricular tissue of comparable age. The results indicate immaturity of the sarcoplasmic reticulum and the beta-adrenergic response of iPS-CMs and ESC-CMs.
KW - Adrenergic beta-Agonists
KW - Animals
KW - Biomechanical Phenomena
KW - Calcium
KW - Calcium Channel Blockers
KW - Cell Culture Techniques
KW - Cell Differentiation
KW - Coculture Techniques
KW - Embryonic Stem Cells
KW - Heart Ventricles
KW - Induced Pluripotent Stem Cells
KW - Mice
KW - Myocardial Contraction
KW - Myocytes, Cardiac
KW - Nifedipine
KW - Sarcoplasmic Reticulum
U2 - 10.1096/fj.09-145177
DO - 10.1096/fj.09-145177
M3 - Journal articles
C2 - 20371616
SN - 1530-6860
SN - 0892-6638
VL - 24
SP - 2739
EP - 2751
JO - FASEB journal : official publication of the Federation of American Societies for Experimental Biology
JF - FASEB journal : official publication of the Federation of American Societies for Experimental Biology
IS - 8
ER -