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

机译:心肌细胞的翻译谱确定斑马鱼心脏再生所需的早期Jak1 / Stat3损伤反应

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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.
机译:某些低等脊椎动物(例如斑马鱼)在心脏受伤后会激活多余的心肌细胞增殖,以再生失去的心肌。在这里,我们使用翻译核糖体亲和纯化来分析斑马鱼心肌细胞在心脏再生过程中翻译的RNA。我们确定了创伤,事件伴随细胞因子产生事件后几个Jak1 / Stat3途径成员的动态诱导。心肌细胞中的转基因Stat3抑制作用限制了损伤诱导的增殖和再生,但并未降低动物生长过程中的心脏发生。损伤引起的分泌蛋白Rln3a以Stat3依赖性方式被诱导,Stat3抑制过程中外源性Rln3的传递刺激了心肌细胞的增殖。我们的结果确定了心脏再生必不可少的损伤特异性心肌细胞程序。

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