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Institut für Physiologie und Pathophysiologie

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Stem Cell-Derived Cardiomyocytes for Myocardial Repair


The regenerative potential of the adult heart is very limited and insufficient to replace damaged muscle mass in the diseased heart. Recent advances in cardiac cell therapy and tissue engineering fuel new hope for the development of novel therapeutic approaches with the aim to trigger myocardial regeneration after injury. Stem cell-derived cardiomyocytes represent ideal candidates for cardiac cell-based therapeutic strategies, and current research focuses on the development of cardiac constructs for implantation. Despite the cardiogenic properties of the newly generated cardiomyocytes, these cells present a heterogeneous and immature phenotype, which is more comparable with cardiomyocytes of early developmental stages. However, successful employment of these new cardiomyocytes for myocardial repair demands that the physiological profile of stem cell-derived cardiomyocytes matches with the functional complexity of mature cardiomyocytes. This is currently not the case. We are interested in gaining better insight into the mechanisms that drive cardiac maturation and follow different approaches to enhance the cardiac phenotype of stem cell-derived cardiomyocytes.

Shaping the Heart – Structural and Functional Characterization of Stem Cell-Derived Cardiomyocytes (SC-CMs)

 

The adult mammalian cardiomyocyte is a highly specialized and terminally differentiated cell with distinct structural features, such as a regular transverse (t)-tubular network (Figure 1A) and strict myofilament organization. This precise microarchitecture is a prerequisite for the sophisticated functional specialization of heart cells and provides the basis for local calcium signaling domains and protein interaction clusters for efficient excitation-contraction (EC-) coupling. Lack of this microarchitecture in premature SC-CMs (Figure 1B) strongly limits the efficiency of cell contraction and force production. These deficits may be overcome by triggering cellular maturation through optimized in vitro culture conditions, aiming at better mirroring the in vivo situation. In this project, we test the hypothesis that a specific cell geometry influences the subcellular microarchitecture of SC-CMs with the aim to trigger morphological and functional maturation in these cells and to approach a similar phenotype as mature myocytes.

 

Figure 1: Comparison of murine adult ventricular cardiomyocytes (A) and induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs, B). Membrane-specific stainings reveal clear differences in the structural organization of both cardiomyocytes. The membrane-specific indicator di-8-anepps was used to mark the sarcolemma. The rectangular shape and regularly spaced transverse (t)-tubular membrane invaginations (see insert) are characteristic for adult cardiomyocytes, while IPSC-CMs do not present any specific cell geometry or regular t-tubular network.

 

In a multi-disciplinary approach combining the expertise in material science and bio-engineering with cardiac cell physiology, we analyze the effects of material contact and specific predefined geometries on cell shape and function at the level of single cells (Figure 2).

 

Figure 2: Different geometries induce structural remodeling in SC-CMs (α-actinin stainings).

 

This project is part of the research bridge “Synthetic Biology” established by HEiKA and a collaboration with the lab of Prof. Dr. Martin Bastmeyer at the Karlsruhe Institute of Technology.

Intercellular Communication in Stem Cell-Derived Cardiomyocytes

 

In the light of novel treatment options for ischemic myopathies and arrhythmogenic diseases, the functional properties of newly developed cardiomyocytes derived from pluripotent stem cells are investigated and compared with primary cardiomyocytes at the cellular level and in multicellular preparations. One critical shortcoming of these cells is their limited potential to connect with native cardiomyocytes in order to establish a functional syncytium (Figure 3). We have recently shown that single SC-CMs present cardiogenic characteristics, however, in multicellular preparations cell-to-cell coupling is strongly compromised. Reduced coupling results in a strong reduction in electrical signal transmission and conduction velocity, which may increase the risk for the development of arrhythmias.

 

In this project, we are interested in the mechanisms that control intercellular communication with the aim to enhance signal transmission in SC-CMs and to improve heterocellular coupling with native cardiomyocytes (Figure 4).

 

Figure 3: Cardiomyocytes form intercellular gap junctions preferentially at the intercalated disks (ICDs), which are located at the end-to-end connections between cells. ICDs in SC-CMs are shown in the elelctron photomicrograph.


 

 

 

 

 

Figure 4: Illustration of the experimental setup to study intercellular coupling.

New Molecular Targets for the Treatment of Cardiac Diseases and Cellular Remodeling

 

In this project we are interested in the molecular determinants that underlie cardiomyocyte remodeling in hypertrophy and arrhythmogenic diseases. Chronic stress affects intracellular signaling cascades that are under control of adrenergic receptors, resulting in maladaptive functional changes and significant alterations of the Ca2+ handling machinery of the cardiomyocyte. We investigate the impact of stress-induced transcriptional changes on cardiac function at the level of sarcolemmal Ca2+-handling proteins and Ca2+ channels of the sarcoplasmic reticulum. Novel pharmacological compounds are tested for their capability of reversing pathological remodeling at the cellular level (Figure 5).

 

Figure 5: Cardiac excitation-contraction coupling and Ca2+ current properties. Left: Ca2+-induced Ca2+ release in adult ventricular cardiomyocytes. L-type Ca2+ currents are elicited by depolarization to different membrane potentials. In parallel, cytosolic Ca2+ levels are monitored in the line-scan mode using a Ca2+-sensitive fluorescent indicator. Right: activation and inactivation curves of the L-type Ca2+ channel under control conditions (black) and in the presence of two compounds with different effects on the channel kinetics (red, blue).

Methods

 

Cell culture

 

  • Heart isolations using Langendorff apparatus (Figure 6)
  • Cardiac cell culture
  • Tissue engineering

Functional studies

 

  • Electrophysiology: patch clamp technique (voltage clamp and current clamp), electrical field stimulation
  • Confocal live cell imaging in parallel with electrophysiological measurements (Figure 7)
  • Contraction studies using edge detection, combined with cytosolic Ca2+ measurements
  • Pharmacological tests

Structural studies

 

  • Immunocytochemistry and confocal imaging
  • Electron microscopy (TEM, Figure 3)

Figure 6: Cardiac cell isolation by enzymatic dissociation.


Figure 7: Simultaneous recordings of membrane currents using voltage clamp and Ca2+ transients by confocal imaging of fluo-3 in the linescan mode. Ca2+ transients are elicited by depolarization (left panels) or caffeine application (right panels).


Neue Publikationen

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Hypertension-evoked RhoA activity in vascular smooth muscle cells requires RGS5. FASEB J. 2017 Dec 5. pii: fj.201700384RR. doi: 10.1096/fj.201700384RR. [Epub ahead of print]

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Modulation of glutathione peroxidase activity by age-dependent carbonylation in glomeruli of diabetic mice. J Diabetes Complications. 2017 Nov 22. pii: S1056-8727(17)31094-2. doi: 10.1016/j.jdiacomp.2017.11.007. [Epub ahead of print]

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Sensitive mass spectrometric assay for determination of 15-deoxy-Δ12,14-prostaglandin J2 and its application in human plasma samples of patients with diabetes. Anal Bioanal Chem. 2017 Nov 16. doi: 10.1007/s00216-017-0748-1. [Epub ahead of print]

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Role of protein carbonylation in diabetes. J Inherit Metab Dis. 2017 Nov 6. doi: 10.1007/s10545-017-0104-9. [Epub ahead of print]

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AP-1 Oligodeoxynucleotides Reduce Aortic Elastolysis in a Murine Model of Marfan Syndrome. Mol Ther Nucleic Acids. 2017 Dec 15; 9: 69–79. Epub 2017 Sep 20. doi: 10.1016/j.omtn.2017.08.014

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Allosteric inhibition of carnosinase (CN1) by inducing a conformational shift. J Enzyme Inhib Med Chem. 2017 Dec;32(1):1102-1110. doi: 10.1080/14756366.2017.1355793.

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Transcription factor decoy technology: a therapeutic update. Biochem Pharmacol. 2017 Nov 15;144:29-34. doi: 10.1016/j.bcp.2017.06.122. Epub 2017 Jun 19. Review.

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Local oxygen homeostasis during various neuronal network activity states in the mouse hippocampus. J Cereb Blood Flow Metab. 2017 Nov 3; 271678X17740091. doi: 10.1177/0271678X17740091

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Subtype-specific differentiation of cardiac pacemaker cell clusters from human induced pluripotent stem cells. Stem Cell Res Ther. 2017 Oct 16;8(1):229. doi: 10.1186/s13287-017-0681-4.

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Heteromeric channels formed by TRPC1, TRPC4 and TRPC5 define hippocampal synaptic transmission and working memory. EMBO J. 2017 Sep 15;36(18):2770-2789. doi: 10.15252/embj.201696369. Epub 2017 Aug 8


Institut für
Physiologie und Pathophysiologie

Universität Heidelberg

Im Neuenheimer Feld 326

69120 Heidelberg

Telefon:+49 6221 54-4056
Telefax:+49 6221 54-6364
E-Mail:susanne.bechtel@
physiologie.uni-heidelberg.de