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Open AccessJournal ArticleDOI

Biowire: a platform for maturation of human pluripotent stem cell-derived cardiomyocytes

TLDR
It is demonstrated that the engineered platform allows for the generation of three-dimensional, aligned cardiac tissues (biowires) with frequent striations and that the responses of immature human myocardium to electrical stimulation and pacing are in agreement with cardiomyocyte maturation.
Abstract
Directed differentiation protocols enable derivation of cardiomyocytes from human pluripotent stem cells (hPSCs) and permit engineering of human myocardium in vitro However, hPSC-derived cardiomyocytes are reflective of very early human development, limiting their utility in the generation of in vitro models of mature myocardium Here we describe a platform that combines three-dimensional cell cultivation with electrical stimulation to mature hPSC-derived cardiac tissues We used quantitative structural, molecular and electrophysiological analyses to explain the responses of immature human myocardium to electrical stimulation and pacing We demonstrated that the engineered platform allows for the generation of three-dimensional, aligned cardiac tissues (biowires) with frequent striations Biowires submitted to electrical stimulation had markedly increased myofibril ultrastructural organization, elevated conduction velocity and improved both electrophysiological and Ca(2+) handling properties compared to nonstimulated controls These changes were in agreement with cardiomyocyte maturation and were dependent on the stimulation rate

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Journal ArticleDOI

Advanced maturation of human cardiac tissue grown from pluripotent stem cells

TL;DR: Tissue maturity was necessary for achieving physiological responses to isoproterenol and recapitulating pathological hypertrophy, supporting the utility of this tissue model for studies of cardiac development and disease.
Journal ArticleDOI

Engineering Adolescence Maturation of Human Pluripotent Stem Cell–Derived Cardiomyocytes

TL;DR: Progress in promoting the maturation of the hPSC cardiomyocytes is discussed, in the context of the current knowledge of developmental cardiac maturation and in relation to in vitro model systems such as rodent ventricular myocytes.
Journal ArticleDOI

Advances in organ-on-a-chip engineering

TL;DR: This Review examines how tissue barrier properties, parenchymal tissue function and multi-organ interactions can be recreated in organ-on-a-chip systems and applied for drug screening.
References
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Journal ArticleDOI

Human embryonic stem cells can differentiate into myocytes with structural and functional properties of cardiomyocytes.

TL;DR: The human ES cell--derived cardiomyocytes displayed structural and functional properties of early-stage cardiomers, which may have significant impact on the study of early human cardiac differentiation, functional genomics, pharmacological testing, cell therapy, and tissue engineering.
Journal ArticleDOI

Cardiac Hypertrophy: The Good, the Bad, and the Ugly

TL;DR: Recent insights into hypertrophic signaling are summarized, several novel antihypertrophic strategies are considered and modulation of myocardial growth without adversely affecting contractile function is increasingly recognized as a potentially auspicious approach in the prevention and treatment of heart failure.
Journal ArticleDOI

Human cardiovascular progenitor cells develop from a KDR + embryonic-stem-cell-derived population

TL;DR: Analysis of the development of the cardiovascular lineages in human embryonic stem cell differentiation cultures identifies a human cardiovascular progenitor that defines one of the earliest stages of human cardiac development.
Journal ArticleDOI

Functional Cardiomyocytes Derived From Human Induced Pluripotent Stem Cells

TL;DR: It is concluded that human iPS cells are a viable option as an autologous cell source for cardiac repair and a powerful tool for cardiovascular research.
PatentDOI

Differentiation of human embryonic stem cells to cardiomyocytes

TL;DR: This is the first demonstration of induction ofcardiomyocyte differentiation in hES cells that do not undergo spontaneous cardiogenesis and provides a model for the study of human cardiomyocytes in culture and could be a step forward in the development of cardiomeocyte transplantation therapies.
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