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核心蛋白聚糖通过调控血管生成过程中的内皮细胞-基质相互作用而起作用。

Decorin regulates endothelial cell-matrix interactions during angiogenesis.

机构信息

Clinical Pharmacology, Rayne Institute, University College London, London, UK.

出版信息

Cell Adh Migr. 2009 Jan-Mar;3(1):3-6. doi: 10.4161/cam.3.1.7275. Epub 2009 Jan 24.

Abstract

Interactions between endothelial cells and the surrounding extracellular matrix are continuously adapted during angiogenesis, from early sprouting through to lumen formation and vessel maturation. Regulated control of these interactions is crucial to sustain normal responses in this rapidly changing environment, and dysfunctional endothelial cell behaviour results in angiogenic disorders. The proteoglycan decorin, an extracellular matrix component, is upregulated during angiogenesis. While it was shown previously that the absence of decorin leads to dysregulated angiogenesis in vivo, the molecular mechanisms were not clear. These abnormal endothelial cell responses have been attributed to indirect effects of decorin; however, our recent data provides evidence that decorin directly regulates endothelial cell-matrix interactions. This data will be discussed in conjunction with findings from previous studies, to better understand the role of this proteoglycan in angiogenesis.

摘要

在内皮细胞和周围细胞外基质的相互作用在血管生成过程中不断适应,从早期的发芽到管腔形成和血管成熟。对这些相互作用的调节控制对于维持这个快速变化环境中的正常反应至关重要,而内皮细胞功能障碍会导致血管生成障碍。蛋白聚糖decorin 是细胞外基质的成分,在血管生成过程中上调。虽然之前已经表明 decorin 的缺失会导致体内血管生成失调,但分子机制尚不清楚。这些异常的内皮细胞反应归因于 decorin 的间接作用;然而,我们最近的数据提供了证据表明 decorin 直接调节内皮细胞-基质相互作用。这将与以前的研究结果一起讨论这些数据,以更好地了解这种蛋白聚糖在血管生成中的作用。

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