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Hippo Signaling Mediators Yap and Taz Are Required in the Epicardium for Coronary Vasculature Development.在冠状动脉血管发育过程中,心外膜需要Hippo信号通路的介质Yap和Taz。
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2
Hippo Signaling Plays an Essential Role in Cell State Transitions during Cardiac Fibroblast Development.Hippo 信号通路在心脏成纤维细胞发育过程中的细胞状态转变中发挥着重要作用。
Dev Cell. 2018 Apr 23;45(2):153-169.e6. doi: 10.1016/j.devcel.2018.03.019.
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YAP and TAZ Negatively Regulate Prox1 During Developmental and Pathologic Lymphangiogenesis.YAP 和 TAZ 在发育和病理性淋巴管生成过程中负调控 Prox1。
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Epicardial CCM2 Promotes Cardiac Development and Repair Via its Regulation on Cytoskeletal Reorganization.心外膜CCM2通过对细胞骨架重组的调控促进心脏发育和修复。
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本文引用的文献

1
Reprogramming of Sertoli cells to fetal-like Leydig cells by Wt1 ablation.通过Wt1基因敲除将支持细胞重编程为胎儿样睾丸间质细胞。
Proc Natl Acad Sci U S A. 2015 Mar 31;112(13):4003-8. doi: 10.1073/pnas.1422371112. Epub 2015 Mar 16.
2
Dual role of YAP and TAZ in renewal of the intestinal epithelium.YAP 和 TAZ 在肠道上皮更新中的双重作用。
Nat Cell Biol. 2015 Jan;17(1):7-19. doi: 10.1038/ncb3084. Epub 2014 Dec 22.
3
The Wilms' tumour suppressor Wt1 is a major regulator of tumour angiogenesis and progression.Wilms 瘤抑制因子 WT1 是肿瘤血管生成和进展的主要调节因子。
Nat Commun. 2014 Dec 16;5:5852. doi: 10.1038/ncomms6852.
4
The sinus venosus contributes to coronary vasculature through VEGFC-stimulated angiogenesis.静脉窦通过VEGFC刺激的血管生成对冠状动脉系统有贡献。
Development. 2014 Dec;141(23):4500-12. doi: 10.1242/dev.113639. Epub 2014 Nov 5.
5
Wt1 dictates the fate of fetal and adult Leydig cells during development in the mouse testis.Wt1 在小鼠睾丸发育过程中决定胎儿和成体莱迪希细胞的命运。
Am J Physiol Endocrinol Metab. 2014 Dec 15;307(12):E1131-43. doi: 10.1152/ajpendo.00425.2014. Epub 2014 Oct 21.
6
Tbx5 is required for avian and Mammalian epicardial formation and coronary vasculogenesis.Tbx5对于鸟类和哺乳动物的心外膜形成及冠状动脉血管生成是必需的。
Circ Res. 2014 Oct 24;115(10):834-44. doi: 10.1161/CIRCRESAHA.115.304379. Epub 2014 Sep 22.
7
Hippo pathway activity influences liver cell fate.河马通路活性影响肝细胞命运。
Cell. 2014 Jun 5;157(6):1324-1338. doi: 10.1016/j.cell.2014.03.060.
8
Yap1 is required for endothelial to mesenchymal transition of the atrioventricular cushion.Yap1是房室垫内皮向间充质转化所必需的。
J Biol Chem. 2014 Jul 4;289(27):18681-92. doi: 10.1074/jbc.M114.554584. Epub 2014 May 15.
9
The transcriptional regulators TAZ and YAP direct transforming growth factor β-induced tumorigenic phenotypes in breast cancer cells.转录调节因子 TAZ 和 YAP 指导转化生长因子 β 诱导的乳腺癌细胞中的肿瘤发生表型。
J Biol Chem. 2014 May 9;289(19):13461-74. doi: 10.1074/jbc.M113.529115. Epub 2014 Mar 19.
10
Tbx18 regulates development of the epicardium and coronary vessels.Tbx18 调节心外膜和冠状血管的发育。
Dev Biol. 2013 Nov 15;383(2):307-20. doi: 10.1016/j.ydbio.2013.08.019. Epub 2013 Sep 7.

在冠状动脉血管发育过程中,心外膜需要Hippo信号通路的介质Yap和Taz。

Hippo Signaling Mediators Yap and Taz Are Required in the Epicardium for Coronary Vasculature Development.

作者信息

Singh Anamika, Ramesh Sindhu, Cibi Dasan Mary, Yun Lim Sze, Li Jun, Li Li, Manderfield Lauren J, Olson Eric N, Epstein Jonathan A, Singh Manvendra K

机构信息

Program in Cardiovascular and Metabolic Disorders, Duke-NUS Medical School Singapore, Singapore 169857, Singapore.

National Heart Research Institute Singapore, National Heart Center Singapore, Singapore 169609, Singapore.

出版信息

Cell Rep. 2016 May 17;15(7):1384-1393. doi: 10.1016/j.celrep.2016.04.027. Epub 2016 May 5.

DOI:10.1016/j.celrep.2016.04.027
PMID:27160901
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4871746/
Abstract

Formation of the coronary vasculature is a complex and precisely coordinated morphogenetic process that begins with the formation of epicardium. The epicardium gives rise to many components of the coronary vasculature, including fibroblasts, smooth muscle cells, and endothelium. Hippo signaling components have been implicated in cardiac development and regeneration. However, a role of Hippo signaling in the epicardium has not been explored. Employing a combination of genetic and pharmacological approaches, we demonstrate that inhibition of Hippo signaling mediators Yap and Taz leads to impaired epicardial epithelial-to-mesenchymal transition (EMT) and a reduction in epicardial cell proliferation and differentiation into coronary endothelial cells. We provide evidence that Yap and Taz control epicardial cell behavior, in part by regulating Tbx18 and Wt1 expression. Our findings show a role for Hippo signaling in epicardial cell proliferation, EMT, and cell fate specification during cardiac organogenesis.

摘要

冠状动脉血管系统的形成是一个复杂且精确协调的形态发生过程,始于心外膜的形成。心外膜产生冠状动脉血管系统的许多组成部分,包括成纤维细胞、平滑肌细胞和内皮细胞。Hippo信号通路的组成部分与心脏发育和再生有关。然而,Hippo信号在心外膜中的作用尚未得到探索。通过结合遗传和药理学方法,我们证明抑制Hippo信号介质Yap和Taz会导致心外膜上皮-间充质转化(EMT)受损,心外膜细胞增殖减少以及向冠状动脉内皮细胞的分化减少。我们提供的证据表明,Yap和Taz部分通过调节Tbx18和Wt1的表达来控制心外膜细胞行为。我们的研究结果表明,Hippo信号在心脏器官发生过程中的心外膜细胞增殖、EMT和细胞命运决定中发挥作用。