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Pluripotent Stem Cell Derived Cardiac Cells for Myocardial Repair
Published on: February 3, 2017
Stem cells for clinical use in cardiovascular medicine: current limitations and future perspectives
1Hôpital Européen Georges Pompidou, Department of Cardiovascular Surgery, Paris, France. philippe.menasche@hop.egp.ap-hop-paris.fr
Insights
Cell transplantation shows promise for cardiac failure by replacing lost heart cells. Future research focuses on cell types that can integrate electromechanically for true myocardial regeneration.
Area of Science:
- Regenerative Medicine
- Cardiology
- Stem Cell Biology
Background:
- Cell transplantation is a promising strategy for treating cardiac failure by addressing cardiomyocyte loss.
- Autologous skeletal myoblasts and bone marrow stem cells are currently in clinical trials for heart repair.
Purpose of the Study:
- To review the current status and future directions of cell transplantation for cardiac repair.
- To identify key challenges and potential solutions for enhancing cardiac function through cell therapy.
Main Methods:
- Review of experimental studies and early-phase clinical trials on cell transplantation for cardiac repair.
- Analysis of the limitations of current adult stem cell therapies and the potential of novel cell types.
Main Results:
- While cell therapy shows potential, adult stem cells (myogenic or marrow-derived) often fail to electromechanically integrate.
- Cardiac stem cells and cardiac-precommitted embryonic stem cells show promise for true myocardial regeneration.
Conclusions:
- Further research is needed to optimize cell type, delivery, survival, and integration for effective cardiac repair.
- Next-generation cell therapies, particularly those with cardiomyogenic potential, are crucial for enhancing contractile function and regenerating damaged myocardium.
Abstract:
Cell transplantation is currently gaining a growing interest as a potential new means of improving the prognosis of patients with cardiac failure. The basic assumption is that left ventricular dysfunction is largely due to the loss of a critical number of cardiomyocytes and that it can be partly reversed by implantation of new contractile cells into the postinfarction scars. Primarily for practical reasons, autologous skeletal myoblasts have been the first to undergo clinical trials and now that the feasibility of the procedure is well established, efficacy data are expected from the ongoing randomized studies. Bone marrow stem cells are also generating a great deal of interest, particularly in patients with acute myocardial infarction, and are currently undergoing extensive clinical testing although recent data have raised a cautionary note about the transdifferentiation potential of these cells. While experimental studies and early-phase clinical trials tend to support the concept that cell therapy may enhance cardiac repair, several key issues still need to be addressed including (1) the optimal type of donor cells in relation to the clinical profile of the patients, (2) the mechanism by which cell engraftment improves cardiac function, (3) the optimization of cell survival, (4) the development of less invasive cell delivery techniques and (5) the potential benefits of cell transplantation in nonischemic heart failure. Current evidence suggests, however, that adult stem cells (myogenic or marrow-derived) fail to electromechanically integrate within the recipient heart, thereby mandating the search for second generation cell types able to achieve this goal which is the prerequisite for an effective enhancement of contractile function. Preliminary data suggest that cells that feature a true cardiomyogenic phenotype such as cardiac stem cells and cardiac-precommitted embryonic stem cells may fall in this category and carry the potential for ensuring a true regeneration of dead myocardium.
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