EGFL7与miRNA-126:血管生成联盟

Iva Nikolic, Karl-Heinz Plate, Mirko H H Schmidt
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引用次数: 111

摘要

血管通过严格调控的血管生成和血管生成程序重新形成。这两个过程是不同的,但它们共同的一个步骤是中央管腔的形成,当组织成血管索的细胞群经历复杂的变化以达到管状形态。最近,一种被称为表皮生长因子样结构域7 (EGFL7)的蛋白质被描述为一种新的内皮细胞衍生因子,参与调控维管装配过程中细胞的空间排列。由于其对血管形成和血管形状的影响,EGFL7加入了控制血管形成的大家族分子。直到最近,EGFL7作用的分子机制才开始被阐明,细胞外基质(ECM)的形成以及Notch信号可能在介导其生物学作用中发挥重要作用。此外,敲除动物模型的研究结果表明,位于egfl7基因内的miRNA miR-126通过促进VEGF信号传导、血管生成和血管完整性,在血管发育中发挥重要作用。这篇综述总结了我们目前对EGFL7和miR-126的了解,我们将讨论这两种生物活性分子对血管形成的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

EGFL7 meets miRNA-126: an angiogenesis alliance.

EGFL7 meets miRNA-126: an angiogenesis alliance.

EGFL7 meets miRNA-126: an angiogenesis alliance.

EGFL7 meets miRNA-126: an angiogenesis alliance.

Blood vessels form de novo through the tightly regulated programs of vasculogenesis and angiogenesis. Both processes are distinct but one of the steps they share is the formation of a central lumen, when groups of cells organized as vascular cords undergo complex changes to achieve a tube-like morphology. Recently, a protein termed epidermal growth factor-like domain 7 (EGFL7) was described as a novel endothelial cell-derived factor involved in the regulation of the spatial arrangement of cells during vascular tube assembly. With its impact on tubulogenesis and vessel shape EGFL7 joined the large family of molecules governing blood vessel formation. Only recently, the molecular mechanisms underlying EGFL7's effects have been started to be elucidated and shaping of the extracellular matrix (ECM) as well as Notch signaling might very well play a role in mediating its biological effects. Further, findings in knock-out animal models suggest miR-126, a miRNA located within the egfl7 gene, has a major role in vessel development by promoting VEGF signaling, angiogenesis and vascular integrity. This review summarizes our current knowledge on EGFL7 and miR-126 and we will discuss the implications of both bioactive molecules for the formation of blood vessels.

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