首页> 美国卫生研究院文献>American Journal of Physiology - Lung Cellular and Molecular Physiology >Bioengineering the Lung: Molecules Materials Matrix Morphology and Mechanics: Osteopontin is an endogenous modulator of the constitutively activated phenotype of pulmonary adventitial fibroblasts in hypoxic pulmonary hypertension
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Bioengineering the Lung: Molecules Materials Matrix Morphology and Mechanics: Osteopontin is an endogenous modulator of the constitutively activated phenotype of pulmonary adventitial fibroblasts in hypoxic pulmonary hypertension

机译:肺生物工程:分子材料基质形态和力学:骨桥蛋白是低氧性肺动脉高压中肺外膜成纤维细胞组成型激活表型的内源性调节剂

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摘要

Increased cell proliferation and migration, of several cell types are key components of vascular remodeling observed in pulmonary hypertension (PH). Our previous data demonstrate that adventitial fibroblasts isolated from pulmonary arteries of chronically hypoxic hypertensive calves (termed PH-Fibs) exhibit a “constitutively activated” phenotype characterized by high proliferative and migratory potential. Osteopontin (OPN) has been shown to promote several cellular activities including growth and migration in cancer cells. We thus tested the hypothesis that elevated OPN expression confers the “activated” highly proproliferative and promigratory/invasive phenotype of PH-Fibs. Our results demonstrate that, both in vivo and ex vivo, PH-Fibs exhibited increased expression of OPN, as well as its cognate receptors, αVβ3 and CD44, compared with control fibroblasts (CO-Fibs). Augmented OPN expression in PH-Fibs corresponded to their high proliferative, migratory, and invasive properties and constitutive activation of ERK1/2 and AKT signaling. OPN silencing via small interfering RNA or sequestering OPN production by specific antibodies led to decreased proliferation, migration, invasion, and attenuated ERK1/2, AKT phosphorylation in PH-Fibs. Furthermore, increasing OPN levels in CO-Fibs via recombinant OPN resulted in significant increases in their proliferative, migratory, and invasive capabilities to the levels resembling those of PH-Fibs. Thus our data suggest OPN as an essential contributor to the activated (highly proliferative, migratory, and proinvasive) phenotype of pulmonary adventitial fibroblasts in hypoxic PH.
机译:几种细胞类型中增加的细胞增殖和迁移是在肺动脉高压(PH)中观察到的血管重塑的关键组成部分。我们以前的数据表明,从慢性低氧性高血压小腿的肺动脉(称为PH-Fibs)中分离出的外膜成纤维细胞表现出“组成性激活”表型,其特征是具有高增殖和迁移潜能。骨桥蛋白(OPN)已显示出促进多种细胞活性的作用,包括癌细胞的生长和迁移。因此,我们检验了OPN表达升高赋予PH-Fibs的“活化”高度增殖和迁移/侵袭表型的假说。我们的结果表明,与对照成纤维细胞(CO-Fibs)相比,PH-Fibs在体内和体外均表现出OPN及其相关受体αVβ3和CD44的表达增加。 PH-Fibs中增强的OPN表达与其高增殖,迁移和侵袭特性以及ERK1 / 2和AKT信号的组成型激活相对应。通过小的干扰RNA沉默OPN或通过特异性抗体隔离OPN产生导致PH-Fibs增殖,迁移,侵袭和ERK1 / 2,AKT磷酸化减弱。此外,通过重组OPN增加CO-Fibs中OPN的水平导致其增殖,迁移和侵袭能力显着提高,达到类似于PH-Fibs的水平。因此,我们的数据表明,OPN是低氧PH中肺外膜成纤维细胞活化(高度增殖,迁移和侵袭性)表型的重要贡献者。

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