Literature DB >> 20830688

Signaling pathways in early cardiac development.

Wenrui Liu1, Ann C Foley.   

Abstract

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.
Copyright © 2010 John Wiley & Sons, Inc.

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Mesh:

Year:  2011        PMID: 20830688     DOI: 10.1002/wsbm.112

Source DB:  PubMed          Journal:  Wiley Interdiscip Rev Syst Biol Med        ISSN: 1939-005X


  6 in total

1.  Chemical suppression of specific C-C chemokine signaling pathways enhances cardiac reprogramming.

Authors:  Yijing Guo; Ienglam Lei; Shuo Tian; Wenbin Gao; Karatas Hacer; Yangbing Li; Shaomeng Wang; Liu Liu; Zhong Wang
Journal:  J Biol Chem       Date:  2019-04-25       Impact factor: 5.157

2.  Tmem88a mediates GATA-dependent specification of cardiomyocyte progenitors by restricting WNT signaling.

Authors:  Natasha Novikov; Todd Evans
Journal:  Development       Date:  2013-07-31       Impact factor: 6.868

3.  Irx4 Marks a Multipotent, Ventricular-Specific Progenitor Cell.

Authors:  Daryl O Nelson; Pratik A Lalit; Mitch Biermann; Yogananda S Markandeya; Deborah L Capes; Luke Addesso; Gina Patel; Tianxiao Han; Manorama C John; Patricia A Powers; Karen M Downs; Timothy J Kamp; Gary E Lyons
Journal:  Stem Cells       Date:  2016-09-13       Impact factor: 6.277

4.  Ah Receptor Activation by Dioxin Disrupts Activin, BMP, and WNT Signals During the Early Differentiation of Mouse Embryonic Stem Cells and Inhibits Cardiomyocyte Functions.

Authors:  Qin Wang; Hisaka Kurita; Vinicius Carreira; Chia-I Ko; Yunxia Fan; Xiang Zhang; Jacek Biesiada; Mario Medvedovic; Alvaro Puga
Journal:  Toxicol Sci       Date:  2015-11-15       Impact factor: 4.849

Review 5.  Cardiomyogenesis Modeling Using Pluripotent Stem Cells: The Role of Microenvironmental Signaling.

Authors:  Amanda Leitolis; Anny W Robert; Isabela T Pereira; Alejandro Correa; Marco A Stimamiglio
Journal:  Front Cell Dev Biol       Date:  2019-08-09

6.  DMH1, a novel BMP small molecule inhibitor, increases cardiomyocyte progenitors and promotes cardiac differentiation in mouse embryonic stem cells.

Authors:  Ada Ao; Jijun Hao; Corey R Hopkins; Charles C Hong
Journal:  PLoS One       Date:  2012-07-27       Impact factor: 3.240

  6 in total

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