Quantification of Contractility in Stem Cell-Derived Cardiomyocytes
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Murine embryonic stem cell derived cardiomyocytes (mESC-CMs) and murine induced pluripotent stem cell derived cardiomyocytes (miPS-CMs) were differentiated and co-cultured with irreversibly injured myocardial tissue slices. When beating clusters had integrated morphologically into the damaged tissue, isometric force measurements were performed. Effects of Ca(2+), nifedipine, and beta-adrenergic modulation were studied during loaded contractions and compared with the contractile behavior of native murine myocardial slices. Both CM variants conferred force to the myocardial tissue. Contraction increased with higher concentrations of Ca(2+) and Isoproterenol, and decreased with nifedipine in all slice variants. Differences between mESC-CMs and miPS-CMs were non-significant, however, significantly different (P < 0.05), when compared to native myocardial slices.
KeywordsStem cells iPS Force measurements Damaged myocardium
Therapy for heart failure is a challenge also in the setting of congenital heart disease. Up to now, there is no true solution of a repair of damaged myocytes. Stem cell-derived cardiomyocytes are believed to offer possible solutions in the future. The possibility to potentially replace failing myocardium with stem cell-derived cardiomyocytes will depend to a major part on the contractile properties of these cells.
In order to quantify the contractility of stem cell-derived cardiomyocytes, we present an in vitro model using slices of murine ventricles.
The aim of our work was to compare the contractile properties of (1) murine embryonic stem cell-derived cardiomyocytes (mESC-CMs), (2) murine induced pluripotent stem cell-derived cardiomyocytes (miPS-CMs) and (3) contractile properties of native murine ventricular myocardium at a comparable age of differentiation.
As assumed in a prior work, it is almost impossible to assign myocardial contractile properties of transplanted cells in vivo; we therefore developed a tissue culture model mimicking the situation in vivo .
55.2 Materials and Methods
Experiments were carried out according to the Principles of Laboratory Animal care.
We prepared avital tissue slices from neonatal murine ventricles, which were used as a non-contractile matrix as described elsewhere . In summary, neonatal murine ventricles were embedded in 4% low-melting agarose and cut into 300-μm-thick slices along the short axis with a microtome (Leica Microsystems, Wetzlar, Germany), kept in cold (4 °C) Ca2+-free Tyrode’s solution, continuously aerated with pure oxygen and supplemented with CaCl2 if needed. Finally, the ventricular tissue slices were exposed to irreversible myocardial injury by severe and long-standing deprivation of oxygen and glucose.
MESC-CMs and miPS-CMs were generated as described previously . Beating clusters of miPS-CMs and mESC-CMs were microdissected 11 days after initiation of in vitro differentiation and co-cultured for 5–7 days on top of the oxygen- and glucose-deprived ventricular slices, placing the non-vital slices into a funnel-shaped cavity and adding CM clusters in a very cautious way using a score to estimate attachment and “integration” under microscopic control. For the experiments of contractility measurements, those two types of co-culture preparations and native embryonic heart slices were mounted onto two steel needles connected to an isometric force transducer in a customized dish within Tyrode’s solution. All three types of slices were conditioned stepwise by extending their length until maximal force resulted during continuous pacing at 2–4 Hz. Signals from the force measurement transducer and electrical pacing were A/D converted, amplified and recorded on a digital medium using DASYLab software (National Instruments) with a sampling rate of 1 kHz, high and low pass filtered (0.05–15 Hz) and signal averaged. Isometric force was measured in Tyrode’s solution after 5 min of spontaneous beating at constant resting conditions. The amplitudes of 20 contractions before and after stimulation were normalized and analyzed.
Effects of Ca2+ were analyzed in Ca2+-free Tyrode’s solution by increasing concentrations of Ca2+ (0.5, 2.5, 4.5, 6.5 and 8.5 mM, 10 min for each concentration). In addition, the effects of the Ca2+-blocker nifedipine (0.01–10 M) and ß-adrenergic isoproterenol (10.9–10.6 M) were analyzed.
Means and standard deviations, and ranges were calculated. Paired and unpaired t tests or one-way analysis of variance (ANOVA) was performed. P < 0.05 was considered statistically significant.
The results demonstrate that our ventricular slice model for analysis and comparison of contractility of co-cultured preparations with mESC-CMs, miPS-CMs and native embryonic heart tissue works sufficiently. The primary finding from this study is that stem cell-derived cardiomyocytes, both mESC-CMs and miPS-CMs attached to avital myocardial slices, showed quantifiable force/contractility after co-culture under defined conditions. There were only minor differences between such mESC-CM and miPS-CM preparations. However, significant differences in contraction behavior were found when compared to native embryonic heart slices of comparable age. Calcium dependency was demonstrated in all three preparations in a relative similar fashion, however, in a much lesser amplitude level seen in the pluripotent stem cell-derived cardiomyocyte preparations. MESC-CM and miPS-CM slice preparations exhibited contractile behavior of possibly immature sarcoplasmic reticulum. The Ca2+-channel antagonist nifedipine induced a dose-dependent negative inotropy on the force of contraction of all three preparations underlining the importance of L-type calcium channels for contractility regulation. The stem cell-derived cardiomyocytes showed significantly diminished ß-adrenergic response compared to native embryonic heart slices.
So far there is no data that convincingly support the hypothesis that pluripotent stem cell-derived cardiomyocytes are capable of developing into a cardiomyocyte phenotype that is identical to mature ventricular cardiomyocytes in vitro . The potential development of mature sarcoplasmatic reticulum in stem cell-derived cardiomyocytes is still an issue, and the understanding of factors involved in differentiation toward a functional and a mature cardiac phenotype is still incomplete .
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