Translational profiling of cardiomyocytes identifies an early Jak1/Stat3 injury response required for zebrafish heart regeneration

被引:157
作者
Fang, Yi
Gupta, Vikas
Karra, Ravi
Holdway, Jennifer E.
Kikuchi, Kazu
Poss, Kenneth D. [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
基金
美国国家卫生研究院;
关键词
TRAP; cardiac regeneration; interleukin; inflammation; endocardium; MYOCARDIAL REGENERATION; CARDIAC FIBROBLASTS; SIGNAL TRANSDUCER; STAT3; PROLIFERATION; ACTIVATION; SURVIVAL; GROWTH; CELLS; INFLAMMATION;
D O I
10.1073/pnas.1309810110
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Certain lower vertebrates like zebrafish activate proliferation of spared cardiomyocytes after cardiac injury to regenerate lost heart muscle. Here, we used translating ribosome affinity purification to profile translating RNAs in zebrafish cardiomyocytes during heart regeneration. We identified dynamic induction of several Jak1/Stat3 pathway members following trauma, events accompanied by cytokine production. Transgenic Stat3 inhibition in cardiomyocytes restricted injury-induced proliferation and regeneration, but did not reduce cardiogenesis during animal growth. The secreted protein Rln3a was induced in a Stat3-dependent manner by injury, and exogenous Rln3 delivery during Stat3 inhibition stimulated cardiomyocyte proliferation. Our results identify an injury-specific cardiomyocyte program essential for heart regeneration.
引用
收藏
页码:13416 / 13421
页数:6
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