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Pluripotent Stem Cell Derived Cardiac Cells for Myocardial Repair
Published on: February 3, 2017
Toward Cardiac Regeneration: Combination of Pluripotent Stem Cell-Based Therapies and Bioengineering Strategies
Marta Mazzola1, Elisa Di Pasquale1,2
1Stem Cell Unit, Humanitas Clinical and Research Center - IRCCS, Rozzano, Italy.
Insights
Induced pluripotent stem cells (iPSCs) and tissue engineering offer new hope for cardiac regeneration. These approaches aim to improve heart repair after injury, overcoming limitations of current therapies for cardiovascular diseases.
Area of Science:
- Regenerative Medicine
- Cardiovascular Research
- Biotechnology
Background:
- Cardiovascular diseases are a leading cause of death globally, with limited cardiac tissue regeneration hindering recovery from ischemic injury.
- Current treatments for heart conditions face challenges in clinical translation due to the heart's poor ability to repair itself, leading to fibrosis and heart failure.
- The discovery of induced pluripotent stem cells (iPSCs) offers a patient-specific, ethically viable alternative to embryonic stem cells for cardiac regeneration.
Purpose of the Study:
- To review advancements in using pluripotent stem cells and tissue engineering for cardiac regenerative therapies.
- To highlight the potential of iPSC-derived cardiomyocytes (CMs) and bioengineered constructs for treating heart disease.
- To discuss the outcomes, limitations, and future clinical translation prospects of these regenerative strategies.
Main Methods:
- Review of current literature on induced pluripotent stem cells (iPSCs) and their differentiation into cardiomyocytes (CMs).
- Exploration of tissue-engineering strategies, including 3D structures and organoids, to enhance iPSC-derived CM survival and function.
- Investigation of direct fibroblast-to-cardiomyocyte conversion as a novel approach for in situ cardiac regeneration.
Main Results:
- iPSCs can be differentiated into cardiomyocytes, offering regenerative potential for damaged heart tissue.
- Bioengineering approaches are improving the survival and functionality of iPSC-derived CMs through 3D constructs and organoids.
- Direct conversion of fibroblasts to CMs shows promise for in situ cardiac repair.
Conclusions:
- Pluripotent stem cells and tissue engineering represent a significant advancement in cardiac regenerative medicine.
- Overcoming challenges like poor cell grafting and potential adverse effects is crucial for clinical application.
- Further research and development are needed to translate these promising regenerative approaches into effective clinical treatments for heart failure.
Abstract:
Cardiovascular diseases represent the major cause of morbidity and mortality worldwide. Multiple studies have been conducted so far in order to develop treatments able to prevent the progression of these pathologies. Despite progress made in the last decade, current therapies are still hampered by poor translation into actual clinical applications. The major drawback of such strategies is represented by the limited regenerative capacity of the cardiac tissue. Indeed, after an ischaemic insult, the formation of fibrotic scar takes place, interfering with mechanical and electrical functions of the heart. Hence, the ability of the heart to recover after ischaemic injury depends on several molecular and cellular pathways, and the imbalance between them results into adverse remodeling, culminating in heart failure. In this complex scenario, a new chapter of regenerative medicine has been opened over the past 20 years with the discovery of induced pluripotent stem cells (iPSCs). These cells share the same characteristic of embryonic stem cells (ESCs), but are generated from patient-specific somatic cells, overcoming the ethical limitations related to ESC use and providing an autologous source of human cells. Similarly to ESCs, iPSCs are able to efficiently differentiate into cardiomyocytes (CMs), and thus hold a real regenerative potential for future clinical applications. However, cell-based therapies are subjected to poor grafting and may cause adverse effects in the failing heart. Thus, over the last years, bioengineering technologies focused their attention on the improvement of both survival and functionality of iPSC-derived CMs. The combination of these two fields of study has burst the development of cell-based three-dimensional (3D) structures and organoids which mimic, more realistically, the in vivo cell behavior. Toward the same path, the possibility to directly induce conversion of fibroblasts into CMs has recently emerged as a promising area for in situ cardiac regeneration. In this review we provide an up-to-date overview of the latest advancements in the application of pluripotent stem cells and tissue-engineering for therapeutically relevant cardiac regenerative approaches, aiming to highlight outcomes, limitations and future perspectives for their clinical translation.
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