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Bioengineering the Lung: Molecules Materials Matrix Morphology and Mechanics: PEDF expression regulates the proangiogenic and proinflammatory phenotype of the lung endothelium

机译:肺的生物工程:分子材料基质形态和力学:PEDF表达调节肺内皮的促血管生成和促炎表型

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摘要

Pigment epithelium-derived factor (PEDF) is a multifunctional protein with important roles in regulation of inflammation and angiogenesis. It is produced by various cell types, including endothelial cells (EC). However, the cell autonomous impact of PEDF on EC function needs further investigation. Lung EC prepared from PEDF-deficient (PEDF−/−) mice were more migratory and failed to undergo capillary morphogenesis in Matrigel compared with wild type (PEDF+/+) EC. Although no significant differences were observed in the rates of apoptosis in PEDF−/− EC compared with PEDF+/+ cells under basal or stress conditions, PEDF−/− EC proliferated at a slower rate. PEDF−/− EC also expressed increased levels of proinflammatory markers, including vascular endothelial growth factor, inducible nitric oxide synthase, vascular cell adhesion molecule-1, as well as altered cellular junctional organization, and nuclear localization of β-catenin. The PEDF−/− EC were also more adhesive, expressed decreased levels of thrombospondin-2, tenascin-C, and osteopontin, and increased fibronectin. Furthermore, we showed lungs from PEDF−/− mice exhibited increased expression of macrophage marker F4/80, along with increased thickness of the vascular walls, consistent with a proinflammatory phenotype. Together, our data suggest that the PEDF expression makes significant contribution to modulation of the inflammatory and angiogenic phenotype of the lung endothelium.
机译:色素上皮衍生因子(PEDF)是一种多功能蛋白,在调节炎症和血管生成中具有重要作用。它由多种细胞类型产生,包括内皮细胞(EC)。但是,PEDF对EC功能的细胞自主影响还需要进一步研究。与野生型(PEDF + / +)EC相比,用PEDF缺陷(PEDF-/-)小鼠制备的肺EC更具迁移性,并且在Matrigel中未能进行毛细管形态发生。尽管在基础或应激条件下与PEDF + / +细胞相比,PEDF-/-EC的细胞凋亡率没有显着差异,但PEDF-/-EC的增殖速度较慢。 PEDF-/-EC还表达了增加的促炎性标志物,包括血管内皮生长因子,诱导型一氧化氮合酶,血管细胞粘附分子-1,以及改变的细胞接头组织和β-catenin的核定位。 PEDF-/-EC也更具粘性,表达的血小板反应蛋白2,腱生蛋白C和骨桥蛋白水平降低,而纤连蛋白水平升高。此外,我们显示来自PEDF-/-小鼠的肺表现出增加的巨噬细胞标记F4 / 80表达,以及血管壁厚度增加,与促炎表型一致。在一起,我们的数据表明,PEDF的表达对肺内皮的炎性和血管生成表型的调制作出了重大贡献。

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