Gemberling Matthew, Karra Ravi, Dickson Amy L, Poss Kenneth D
Department of Cell Biology, Howard Hughes Medical Institute, Duke University Medical Center, Durham, United States.
Elife. 2015 Apr 1;4:e05871. doi: 10.7554/eLife.05871.
Heart regeneration is limited in adult mammals but occurs naturally in adult zebrafish through the activation of cardiomyocyte division. Several components of the cardiac injury microenvironment have been identified, yet no factor on its own is known to stimulate overt myocardial hyperplasia in a mature, uninjured animal. In this study, we find evidence that Neuregulin1 (Nrg1), previously shown to have mitogenic effects on mammalian cardiomyocytes, is sharply induced in perivascular cells after injury to the adult zebrafish heart. Inhibition of Erbb2, an Nrg1 co-receptor, disrupts cardiomyocyte proliferation in response to injury, whereas myocardial Nrg1 overexpression enhances this proliferation. In uninjured zebrafish, the reactivation of Nrg1 expression induces cardiomyocyte dedifferentiation, overt muscle hyperplasia, epicardial activation, increased vascularization, and causes cardiomegaly through persistent addition of wall myocardium. Our findings identify Nrg1 as a potent, induced mitogen for the endogenous adult heart regeneration program.
心脏再生在成年哺乳动物中是有限的,但在成年斑马鱼中可通过心肌细胞分裂的激活自然发生。心脏损伤微环境的几个组成部分已被确定,但目前已知没有任何一个因素能在成熟、未受伤的动物中刺激明显的心肌增生。在本研究中,我们发现有证据表明,之前显示对哺乳动物心肌细胞有促有丝分裂作用的神经调节蛋白1(Nrg1),在成年斑马鱼心脏受伤后,在血管周围细胞中被急剧诱导。抑制Nrg1的共同受体Erbb2会破坏心肌细胞对损伤的增殖反应,而心肌中Nrg1的过表达则会增强这种增殖。在未受伤的斑马鱼中,Nrg1表达的重新激活会诱导心肌细胞去分化、明显的肌肉增生、心外膜激活、血管生成增加,并通过持续添加心肌壁导致心脏肥大。我们的研究结果表明,Nrg1是内源性成年心脏再生程序的一种强效诱导有丝分裂原。