Differentiation of pluripotent embryonic stem cells into cardiomyocytes

被引:556
作者
Boheler, KR
Czyz, J
Tweedie, D
Yang, HT
Anisimov, SV
Wobus, AM
机构
[1] NIA, Cardiovasc Sci Lab, Ctr Gerontol Res, NIH, Baltimore, MD 21224 USA
[2] Inst Plant Genet, Gatersleben, Germany
关键词
embryonic stem; embryonic carcinoma; embryonic germ; in vitro differentiation; cardiornyocytes;
D O I
10.1161/01.RES.0000027865.61704.32
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:189 / 201
页数:13
相关论文
共 95 条
[1]   Discovering altered genomic expression patterns in heart: transcriptome determination by serial analysis of gene expression [J].
Anisimov, SV ;
Lakatta, EG ;
Boheler, KR .
EUROPEAN JOURNAL OF HEART FAILURE, 2001, 3 (03) :271-281
[2]  
ANISIMOV SV, IN PRESS MECH DEV
[3]   Leukemia inhibitory factor modulates cardiogenesis in embryoid bodies in opposite fashions [J].
Bader, A ;
Al-Dubai, H ;
Weitzer, G .
CIRCULATION RESEARCH, 2000, 86 (07) :787-794
[4]   Paracrine promotion of cardiomyogenesis in embryoid bodies by LIF modulated endoderm [J].
Bader, A ;
Gruss, A ;
Höllrigl, A ;
Al-Dubai, H ;
Capetanaki, Y ;
Weitzer, G .
DIFFERENTIATION, 2001, 68 (01) :31-43
[5]   In vitro preselection of gene-trapped embryonic stem cell clones for characterizing novel developmentally regulated genes in the mouse [J].
Baker, RK ;
Haendel, MA ;
Swanson, BJ ;
Shambaugh, JC ;
Micales, BK ;
Lyons, GE .
DEVELOPMENTAL BIOLOGY, 1997, 185 (02) :201-214
[6]   The evolving concept of a stem cell: Entity or function? [J].
Blau, HM ;
Brazelton, TR ;
Weimann, JM .
CELL, 2001, 105 (07) :829-841
[7]   Sinoatrial nodal cell ryanodine receptor and Na+-Ca2+ exchanger -: Molecular partners in pacemaker regulation [J].
Bogdanov, KY ;
Vinogradova, TM ;
Lakatta, EG .
CIRCULATION RESEARCH, 2001, 88 (12) :1254-1258
[8]   Can exogenous stem cells be used in transplantation? [J].
Boheler, KR ;
Fiszman, MY .
CELLS TISSUES ORGANS, 1999, 165 (3-4) :237-245
[9]  
BOHELER KR, 2002, ADV CELL AGING GERON, V9, P141
[10]   Efficient gene trap screening for novel developmental genes using IRESβgeo vector and in vitro preselection [J].
Bonaldo, P ;
Chowdhury, K ;
Stoykova, A ;
Torres, M ;
Gruss, P .
EXPERIMENTAL CELL RESEARCH, 1998, 244 (01) :125-136