2026· American Journal of Student Research· pp. 867-875· 0 citations
TL;DR
This study evaluates the role of iPSCs and different biofabrication methods, such as bioprinting, used to create ventricular constructs and cardiac patches that support injured regions of the heart post-MI.
Abstract
Cardiovascular disease is the leading cause of death worldwide, often resulting in a myocardial
infarction (MI), which can lead to irreversible cell death and heart failure (HF). While advances in
bioengineering and regenerative medicine offer promising solutions for patients, traditional heart
transplantations are limited due to a shortage of organ donors. To address this issue, differentiating
induced pluripotent stem cells (iPSCs) into cardiomyocytes via signaling pathways can provide a patientspecific
source of functional cardiomyocytes, and as a long-term goal it may be capable of replacing
damaged myocardial tissue. This study evaluates the role of iPSCs and different biofabrication methods,
such as bioprinting, used to create ventricular constructs and cardiac patches that support injured regions
of the heart post-MI. However, for patients with HF, bioprinting a whole-heart construct is being explored
as a future objective and is necessary to restore cardiac function when cardiac patches or ventricular
constructs are not sufficient. Despite the progress made in the field, few studies have addressed the
need to improve bioprinting vascular networks, adopt appropriate bioinks, and reduce costs for iPSC
differentiation and bioprinting technologies. If successful, this work can eventually mitigate symptoms
post-MI or contribute to addressing HF solutions, offering patients a new quality of life.
Myocardial infarction (MI) remains a leading cause of death worldwide, and therapies that limit injury, promote repair, and restore cardiac function remain limited. Human induced pluripotent stem cells (hiPSCs) provide a renewable source of patient-specific cardiac cells and have enabled the development of increasingly...
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