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冠状动脉的形成是由 R-spondin3 的局部表达所驱动的。

Coronary Artery Formation Is Driven by Localized Expression of R-spondin3.

机构信息

Université Côte d'Azur, Inserm, CNRS, iBV, Nice, 06108, France.

MRC Human Genetics Unit, Western General Hospital, Edinburgh EH42XU, UK.

出版信息

Cell Rep. 2017 Aug 22;20(8):1745-1754. doi: 10.1016/j.celrep.2017.08.004.

Abstract

Coronary arteries are essential to support the heart with oxygen, and coronary heart disease is one of the leading causes of death worldwide. The coronary arteries form at highly stereotyped locations and are derived from the primitive vascular plexus of the heart. How coronary arteries are remodeled and the signaling molecules that govern this process are poorly understood. Here, we have identified the Wnt-signaling modulator Rspo3 as a crucial regulator of coronary artery formation in the developing heart. Rspo3 is specifically expressed around the coronary stems at critical time points in their development. Temporal ablation of Rspo3 at E11.5 leads to decreased β-catenin signaling and a reduction in arterial-specific proliferation. As a result, the coronary stems are defective and the arterial tree does not form properly. These results identify a mechanism through which localized expression of RSPO3 induces proliferation of the coronary arteries at their stems and permits their formation.

摘要

冠状动脉是为心脏提供氧气的重要组成部分,而冠心病是全球范围内导致死亡的主要原因之一。冠状动脉在高度定型的位置形成,来源于心脏原始的血管丛。冠状动脉如何重塑,以及调控这一过程的信号分子还知之甚少。在这里,我们发现 Wnt 信号调节剂 Rspo3 是心脏发育过程中冠状动脉形成的关键调节因子。Rspo3 特异性地在冠状动脉干周围表达,在其发育的关键时间点。E11.5 时 Rspo3 的瞬时消融导致 β-catenin 信号降低和动脉特异性增殖减少。结果,冠状动脉干出现缺陷,动脉树无法正常形成。这些结果确定了一种机制,通过该机制,RSPO3 的局部表达诱导冠状动脉干的增殖,并允许它们形成。

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