Caldesmon is essential for cardiac morphogenesis and function: In vivo study using a zebrafish model

被引:11
作者
Zheng, Ping-Pin [1 ]
Severijnen, Lies-Anne [2 ]
Willemsen, Rob [2 ]
Kros, Johan M. [1 ]
机构
[1] Erasmus MC, Dept Pathol, NL-3000 DR Rotterdam, Netherlands
[2] Erasmus MC, Rotterdam, Netherlands
关键词
Cardiac development; Myogenesis; Contractility; Caldesmon; Zebrafish model; DIFFERENTIAL EXPRESSION; SMOOTH-MUSCLE; HEART TUBE; NEOVASCULARIZATION; GLIOMA; MARKER; CELLS;
D O I
10.1016/j.bbrc.2008.10.165
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The zebrafish homologue of caldesmon is similar to the mammalian low molecular weight caldesmon (l-CaD). In this study, we explored the effects of caldesmon knockdown on vertebrate heart development in vivo. In a zebrafish model caldesmon was knocked down resulting in defective cardiac morphogenesis, muscularization and function. The data provide the first functional assessment of the role of caldesmon in cardiac development in vivo, and indicate that caldesmon is essential for proper cardiac organogenesis and function. Because caldesmon expression remarkably influences cardiac muscularization, the findings are relevant for designing future therapeutic strategies in the regeneration of cardiac damage. (C) 2008 Elsevier Inc. All rights reserved
引用
收藏
页码:37 / 40
页数:4
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