Signaling pathways in early cardiac development

被引:12
作者
Liu, Wenrui [1 ]
Foley, Ann C. [1 ]
机构
[1] Cornell Univ, Greenberg Div Cardiol, Dept Med, Weill Med Coll, New York, NY 10021 USA
关键词
EMBRYONIC STEM-CELLS; CARDIOVASCULAR PROGENITOR CELLS; BONE MORPHOGENETIC PROTEINS; AVIAN PREGASTRULA EPIBLAST; CHEMOKINE RECEPTOR CXCR4; NODAL-RELATED SIGNALS; BETA-CATENIN; HEART FORMATION; XENOPUS-LAEVIS; DEFINITIVE ENDODERM;
D O I
10.1002/wsbm.112
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cardiomyocyte differentiation is a complex multistep process requiring the proper temporal and spatial integration of multiple signaling pathways. Previous embryological and genetic studies have identified a number of signaling pathways that are critical to mediate the initial formation of the mesoderm and its allocation to the cardiomyocyte lineage. It has become clear that some of these signaling networks work autonomously, in differentiating myocardial cells whereas others work non-autonomously, in neighboring tissues, to regulate cardiac differentiation indirectly. Here, we provide an overview of three signaling networks that mediate cardiomyocyte specification and review recent insights into their specific roles in heart development. In addition, we demonstrate how systems level, 'omic approaches' and other high-throughput techniques such as small molecules screens are beginning to impact our understanding of cardiomyocyte specification and, to identify novel signaling pathways involved in this process. In particular, it now seems clear that at least one chemokine receptor CXCR4 is an important marker for cardiomyocyte progenitors and may play a functional role in their differentiation. Finally, we discuss some gaps in our current understanding of early lineage selection that could be addressed by various types of omic analysis. (C) 2010 John Wiley & Sons, Inc. WIREs Syst Biol Med 2011 3 191-205 DOI: 10.1002/wsbm.112
引用
收藏
页码:191 / 205
页数:15
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