Metabolic modulation regulates cardiac wall morphogenesis in zebrafish

被引:21
作者
Fukuda, Ryuichi [1 ]
Aharonov, Alla [2 ]
Ong, Yu Ting [3 ]
Stone, Oliver A. [1 ,4 ]
El-Brolosy, Mohamed [1 ]
Maischein, Hans-Martin [1 ]
Potente, Michael [3 ]
Tzahor, Eldad [2 ]
Stainier, Didier Y. R. [1 ]
机构
[1] Max Planck Inst Heart & Lung Res, Dept Dev Genet, Ludwigstr, Bad Nauheim, Germany
[2] Weizmann Inst Sci, Dept Mol Cell Biol, Rehovot, Israel
[3] Max Planck Inst Heart & Lung Res, Angiogenesis & Metab Lab, Ludwigstr, Bad Nauheim, Germany
[4] Univ Oxford, Dept Physiol Anat & Genet, BHF Ctr Res Excellence, Oxford, England
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; PYRUVATE-DEHYDROGENASE; CARDIOMYOCYTE BEHAVIOR; CANCER; HEART; NEUREGULIN; EXPRESSION; GROWTH; ERBB2; PLASTICITY;
D O I
10.7554/eLife.50161
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
During cardiac development, cardiomyocytes form complex inner wall structures called trabeculae. Despite significant investigation into this process, the potential role of metabolism has not been addressed. Using single cell resolution imaging in zebrafish, we find that cardiomyocytes seeding the trabecular layer actively change their shape while compact layer cardiomyocytes remain static. We show that Erbb2 signaling, which is required for trabeculation, activates glycolysis to support changes in cardiomyocyte shape and behavior. Pharmacological inhibition of glycolysis impairs cardiac trabeculation, and cardiomyocyte-specific loss- and gain-of-function manipulations of glycolysis decrease and increase trabeculation, respectively. In addition, loss of the glycolytic enzyme pyruvate kinase M2 impairs trabeculation. Experiments with rat neonatal cardiomyocytes in culture further support these observations. Our findings reveal new roles for glycolysis in regulating cardiomyocyte behavior during cardiac wall morphogenesis.
引用
收藏
页数:14
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