» Articles » PMID: 12169644

Differentiation of Pluripotent Embryonic Stem Cells into Cardiomyocytes

Overview
Journal Circ Res
Date 2002 Aug 10
PMID 12169644
Citations 233
Authors
Affiliations
Soon will be listed here.
Abstract

Embryonic stem (ES) cells have been established as permanent lines of undifferentiated pluripotent cells from early mouse embryos. ES cells provide a unique system for the genetic manipulation and the creation of knockout strains of mice through gene targeting. By cultivation in vitro as 3D aggregates called embryoid bodies, ES cells can differentiate into derivatives of all 3 primary germ layers, including cardiomyocytes. Protocols for the in vitro differentiation of ES cells into cardiomyocytes representing all specialized cell types of the heart, such as atrial-like, ventricular-like, sinus nodal-like, and Purkinje-like cells, have been established. During differentiation, cardiac-specific genes as well as proteins, receptors, and ion channels are expressed in a developmental continuum, which closely recapitulates the developmental pattern of early cardiogenesis. Exploitation of ES cell-derived cardiomyocytes has facilitated the analysis of early cardiac development and has permitted in vitro "gain-of-function" or "loss-of-function" genetic studies. Recently, human ES cell lines have been established that can be used to investigate cardiac development and the function of human heart cells and to determine the basic strategies of regenerative cell therapy. This review summarizes the current state of ES cell-derived cardiogenesis and provides an overview of how genomic strategies coupled with this in vitro differentiation system can be applied to cardiac research.

Citing Articles

ProteotoxomiRs: Diagnostic and pathologic miRNA signatures for reductive stress induced proteotoxic heart disease.

Karthikeyan S, Nallasamy P, Cleveland J, Arulmani A, Raveendran A, Karimi M Redox Biol. 2025; 81:103525.

PMID: 39986116 PMC: 11893311. DOI: 10.1016/j.redox.2025.103525.


Optimization of H9c2 differentiation leads to calcium-active and striated cardiac cells without addition of retinoic acid.

Brock J, Horning M Front Cell Dev Biol. 2024; 12:1501540.

PMID: 39650723 PMC: 11621855. DOI: 10.3389/fcell.2024.1501540.


Current technology and industrialization status of cell-cultivated meat.

Lee S, Lee D, Yun S, Lee J, Mariano Jr E, Park J J Anim Sci Technol. 2024; 66(1):1-30.

PMID: 38618028 PMC: 11007461. DOI: 10.5187/jast.2023.e107.


Influence of acidic metabolic environment on differentiation of stem cell-derived cardiomyocytes.

Jiahao M, Fan Z, Junsheng M Front Cardiovasc Med. 2024; 11:1288710.

PMID: 38572303 PMC: 10987843. DOI: 10.3389/fcvm.2024.1288710.


Pluripotent stem cells for target organ developmental toxicity testing.

Wu X, Chen Y, Kreutz A, Silver B, Tokar E Toxicol Sci. 2024; 199(2):163-171.

PMID: 38547390 PMC: 11131012. DOI: 10.1093/toxsci/kfae037.