Dependence of Cardiac Trabeculation on Neuregulin Signaling and Blood Flow in Zebrafish

被引:108
作者
Peshkovsky, Courtney [2 ,3 ]
Totong, Ronald [2 ,3 ]
Yelon, Deborah [1 ,2 ,3 ]
机构
[1] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
[2] NYU, Sch Med, Dev Genet Program, Kimmel Ctr Biol & Med,Skirball Inst Biomol Med, New York, NY USA
[3] NYU, Sch Med, Dept Cell Biol, Kimmel Ctr Biol & Med,Skirball Inst Biomol Med, New York, NY 10016 USA
关键词
zebrafish; cardiac morphogenesis; ventricular trabeculation; myocardium; endocardium; cloche; AG1478; weak atrium; DEVELOPING HEART; MORPHOGENESIS; MYOCARDIUM; RECEPTOR; ERBB2; GENE; CARDIOGENESIS; SPECIFICATION; INHIBITION; CLOCHE;
D O I
10.1002/dvdy.22526
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Maturation of the developing heart requires the structural elaboration of the embryonic ventricle through the process of trabeculation. Trabeculae form as the ventricular myocardium protrudes into the lumen of the chamber, thereby increasing muscle mass and altering functional output. Little is understood about the cellular basis for trabeculation and its genetic regulation. Here, we establish the utility of the zebrafish embryo for the analysis of the mechanisms driving trabeculation. In zebrafish, we can follow trabeculation in four dimensions and define morphologically discrete stages for the initiation, propagation, and network elaboration that form the ventricular trabeculae. We find that Neuregulin/ErbB signaling is required for the initial protrusion of the myocardium into the ventricular lumen. Additionally, we demonstrate that optimal blood flow through the ventricle is important for the advancement of trabeculation. Thus, our results indicate that the zebrafish provides a valuable model for investigating possible causes of congenital defects in trabeculation. Developmental Dynamics 240:446-456, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:446 / 456
页数:11
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