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Extrinsic regulation of cardiomyocyte differentiation of embryonic stem cells.

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TLDR
This review will focus on extrinsic factors that play a role in regulating different stages of cardiomyocyte differentiation of ES cells in Pluripotent embryonic stem (ES) cells.
Abstract
Cardiovascular disease is one of leading causes of death throughout the U.S. and the world. The damage of cardiomyocytes resulting from ischemic injury is irreversible and leads to the development of progressive heart failure, which is characterized by the loss of functional cardiomyocytes. Because cardiomyocytes are unable to regenerate in the adult heart, cell-based therapy of transplantation provides a potential alternative approach to replace damaged myocardial tissue and restore cardiac function. A major roadblock toward this goal is the lack of donor cells; therefore, it is urgent to identify the cardiovascular cells that are necessary for achieving cardiac muscle regeneration. Pluripotent embryonic stem (ES) cells have enormous potential as a source of therapeutic tissues, including cardiovascular cells; however, the regulatory elements mediating ES cell differentiation to cardiomyocytes are largely unknown. In this review, we will focus on extrinsic factors that play a role in regulating different stages of cardiomyocyte differentiation of ES cells.

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Electrical stimulation of human embryonic stem cells: cardiac differentiation and the generation of reactive oxygen species.

TL;DR: Cardiac differentiation in these EBs was evidenced by spontaneous contractions, expression of troponin T and its sarcomeric organization, implying that electrical stimulation plays a role in cardiac differentiation of hESCs, through mechanisms associated with the intracellular generation of ROS.
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Present state and future perspectives of using pluripotent stem cells in toxicology research

TL;DR: Methods for differentiation and selection of cardiac and hepatic cells from hPSCs are summarized, requirements and implications with respect to the use of these cells in safety pharmacology and toxicology are presented, and future challenges and perspectives of using hPSC-based cell models are discussed.
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Enhanced differentiation of human embryonic stem cells to mesenchymal progenitors by inhibition of TGF‐β/activin/nodal signaling using SB‐431542

TL;DR: A simple and versatile protocol for directing the differentiation of hESCs into a myogenic lineage and then further into mesenchymal progenitors by blocking the TGF‐β signaling pathway is reported.
Journal ArticleDOI

Genome-wide discovery and analysis of microRNAs and other small RNAs from rice embryogenic callus

TL;DR: Using in vitro cultured embryogenic calli as a model, 53 microRNA or microRNA* sequences appear to vary in expression between differentiated and undifferentiated calli, suggesting a role in meristem development and a new class of plant small RNAs derived from 5’ or 3’ ends of mature tRNA analogous to the tRFs in human cancer cell.
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Hedgehog signaling plays a cell-autonomous role in maximizing cardiac developmental potential

TL;DR: Through fate-mapping, it is found that Hh signaling is required at early stages to ensure specification of the proper number of myocardial progenitors, making it an attractive target for manipulation of multipotent progenitor cells.
References
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Journal ArticleDOI

Notch Signaling: Cell Fate Control and Signal Integration in Development

TL;DR: Notch signaling defines an evolutionarily ancient cell interaction mechanism, which plays a fundamental role in metazoan development, providing a general developmental tool to influence organ formation and morphogenesis.
Journal ArticleDOI

The Oxytocin Receptor System: Structure, Function, and Regulation

TL;DR: The regulation by gonadal and adrenal steroids is one of the most remarkable features of the OT system and is, unfortunately, the least understood.
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Cardiomyocytes derived from human embryonic stem cells in pro-survival factors enhance function of infarcted rat hearts

TL;DR: This work generated highly purified human cardiomyocytes using a readily scalable system for directed differentiation that relies on activin A and BMP4, and identified a cocktail of pro-survival factors that limitsCardiomyocyte death after transplantation.
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Bone morphogenetic protein-4 is required for mesoderm formation and patterning in the mouse.

TL;DR: Results provide direct genetic evidence that BMP-4 is essential for several different processes in early mouse development, beginning with gastrulation and mesoderm formation.
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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.
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