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Hand2 elevates cardiomyocyte production during zebrafish heart development and regeneration

机译:Hand2在斑马鱼心脏发育和再生过程中提高心肌细胞的产生

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摘要

Embryonic heart formation requires the production of an appropriate number of cardiomyocytes; likewise, cardiac regeneration following injury relies upon the recovery of lost cardiomyocytes. The basic helix-loop-helix (bHLH) transcription factor Hand2 has been implicated in promoting cardiomyocyte formation. It is unclear, however, whether Hand2 plays an instructive or permissive role during this process. Here, we find that overexpression of hand2 in the early zebrafish embryo is able to enhance cardiomyocyte production, resulting in an enlarged heart with a striking increase in the size of the outflow tract. Our evidence indicates that these increases are dependent on the interactions of Hand2 in multimeric complexes and are independent of direct DNA binding by Hand2. Proliferation assays reveal that hand2 can impact cardiomyocyte production by promoting division of late-differentiating cardiac progenitors within the second heart field. Additionally, our data suggest that hand2 can influence cardiomyocyte production by altering the patterning of the anterior lateral plate mesoderm, potentially favoring formation of the first heart field at the expense of hematopoietic and vascular lineages. The potency of hand2 during embryonic cardiogenesis suggested that hand2 could also impact cardiac regeneration in adult zebrafish; indeed, we find that overexpression of hand2 can augment the regenerative proliferation of cardiomyocytes in response to injury. Together, our studies demonstrate that hand2 can drive cardiomyocyte production in multiple contexts and through multiple mechanisms. These results contribute to our understanding of the potential origins of congenital heart disease and inform future strategies in regenerative medicine.
机译:胚胎心脏的形成需要产生适当数量的心肌细胞。同样,损伤后的心脏再生依赖于丢失的心肌细胞的恢复。基本的螺旋-环-螺旋(bHLH)转录因子Hand2与促进心肌细胞形成有关。但是,尚不清楚Hand2在此过程中起指导作用还是让步。在这里,我们发现在斑马鱼早期胚胎中过表达hand2能够增强心肌细胞的产生,从而导致心脏扩大,流出道的大小显着增加。我们的证据表明,这些增加取决于Hand2在多聚体复合物中的相互作用,并且独立于Hand2的直接DNA结合。增殖试验表明,hand2可以通过促进第二心脏区域内晚期分化的心脏祖细胞的分裂来影响心肌细胞的产生。此外,我们的数据表明,hand2可以通过改变前外侧板中胚层的模式来影响心肌细胞的产生,可能以造血和血管谱系为代价,有利于形成第一个心脏区域。 hand2在胚胎心脏发生过程中的效力表明,hand2也可能影响成年斑马鱼的心脏再生。确实,我们发现hand2的过表达可以增强心肌细胞对损伤的再生增殖。总之,我们的研究表明hand2可以在多种情况下通过多种机制驱动心肌细胞的产生。这些结果有助于我们了解先天性心脏病的潜在起源,并为再生医学的未来策略提供参考。

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