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本文引用的文献

1
Reciprocal analyses in zebrafish and medaka reveal that harnessing the immune response promotes cardiac regeneration.斑马鱼和青鳉的相互分析表明,利用免疫反应可促进心脏再生。
Elife. 2017 Jun 20;6:e25605. doi: 10.7554/eLife.25605.
2
Notch signalling restricts inflammation and expression in the dynamic endocardium of the regenerating zebrafish heart.Notch信号通路限制再生斑马鱼心脏动态心内膜中的炎症和表达。
Development. 2017 Apr 15;144(8):1425-1440. doi: 10.1242/dev.143362. Epub 2017 Feb 27.
3
Redirecting cardiac growth mechanisms for therapeutic regeneration.重定向心脏生长机制以实现治疗性再生。
J Clin Invest. 2017 Feb 1;127(2):427-436. doi: 10.1172/JCI89786.
4
Hypoxia induces heart regeneration in adult mice.缺氧诱导成年小鼠心脏再生。
Nature. 2017 Jan 12;541(7636):222-227. doi: 10.1038/nature20173. Epub 2016 Oct 31.
5
Fast revascularization of the injured area is essential to support zebrafish heart regeneration.受伤区域的快速血管再生对于支持斑马鱼心脏再生至关重要。
Proc Natl Acad Sci U S A. 2016 Oct 4;113(40):11237-11242. doi: 10.1073/pnas.1605431113. Epub 2016 Sep 19.
6
Coordinating cardiomyocyte interactions to direct ventricular chamber morphogenesis.协调心肌细胞相互作用以指导心室形态发生。
Nature. 2016 Jun 30;534(7609):700-4. doi: 10.1038/nature18310.
7
Modulation of tissue repair by regeneration enhancer elements.再生增强元件对组织修复的调节作用。
Nature. 2016 Apr 14;532(7598):201-6. doi: 10.1038/nature17644. Epub 2016 Apr 6.
8
Multicolor mapping of the cardiomyocyte proliferation dynamics that construct the atrium.构建心房的心肌细胞增殖动力学的多色映射。
Development. 2016 May 15;143(10):1688-96. doi: 10.1242/dev.136606. Epub 2016 Mar 17.
9
Angiocrine functions of organ-specific endothelial cells.器官特异性内皮细胞的血管分泌功能。
Nature. 2016 Jan 21;529(7586):316-25. doi: 10.1038/nature17040.
10
Sequential Notch activation regulates ventricular chamber development.Notch信号的顺序激活调节心室腔的发育。
Nat Cell Biol. 2016 Jan;18(1):7-20. doi: 10.1038/ncb3280. Epub 2015 Dec 7.

Vegfaa 指导成年斑马鱼心肌细胞增生。

Vegfaa instructs cardiac muscle hyperplasia in adult zebrafish.

机构信息

Department of Medicine, Duke University Medical Center, Durham, NC 27710;

Regeneration Next, Duke University, Durham, NC 27110.

出版信息

Proc Natl Acad Sci U S A. 2018 Aug 28;115(35):8805-8810. doi: 10.1073/pnas.1722594115. Epub 2018 Aug 13.

DOI:10.1073/pnas.1722594115
PMID:30104362
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6126768/
Abstract

During heart development and regeneration, coronary vascularization is tightly coupled with cardiac growth. Although inhibiting vascularization causes defects in the innate regenerative response of zebrafish to heart injury, angiogenic signals are not known to be sufficient for triggering regeneration events. Here, by using a transgenic reporter strain, we found that regulatory sequences of the angiogenic factor are active in epicardial cells of uninjured animals, as well as in epicardial and endocardial tissue adjacent to regenerating muscle upon injury. Additionally, we find that induced cardiac overexpression of in zebrafish results in overt hyperplastic thickening of the myocardial wall, accompanied by indicators of angiogenesis, epithelial-to-mesenchymal transition, and cardiomyocyte regeneration programs. Unexpectedly, overexpression in the context of cardiac injury enabled ectopic cardiomyogenesis but inhibited regeneration at the site of the injury. Our findings identify Vegfa as one of a select few known factors sufficient to activate adult cardiomyogenesis, while also illustrating how instructive factors for heart regeneration require spatiotemporal control for efficacy.

摘要

在心脏发育和再生过程中,冠状血管生成与心脏生长紧密耦合。尽管抑制血管生成会导致斑马鱼心脏损伤后的固有再生反应出现缺陷,但血管生成信号不足以引发再生事件。在这里,我们通过使用转基因报告品系发现,血管生成因子的调节序列在未受伤动物的心肌细胞中以及受伤后再生肌肉附近的心外膜和心内膜组织中均具有活性。此外,我们发现,在斑马鱼中诱导心脏过表达导致心肌壁明显的增生性增厚,伴随着血管生成、上皮-间充质转化和心肌细胞再生程序的指标。出乎意料的是,心脏损伤背景下的过表达能够诱导异位心肌发生,但抑制了损伤部位的再生。我们的发现表明,Vegfa 是少数已知足以激活成人心肌发生的因子之一,同时也说明了心脏再生的指令性因子需要时空控制才能发挥作用。