首页> 美国卫生研究院文献>American Journal of Respiratory Cell and Molecular Biology >Targeting Insulin-Like Growth Factor-I and Insulin-Like Growth Factor–Binding Protein-3 Signaling Pathways. A Novel Therapeutic Approach for Asthma
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Targeting Insulin-Like Growth Factor-I and Insulin-Like Growth Factor–Binding Protein-3 Signaling Pathways. A Novel Therapeutic Approach for Asthma

机译:靶向胰岛素样生长因子-I和胰岛素样生长因子结合蛋白-3信号传导途径。一种新型的哮喘治疗方法

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摘要

Insulin-like growth factor (IGF)-I has been recognized to play critical roles in the pathogenesis of asthma, whereas IGF-binding protein (IGFBP)-3 blocks crucial physiologic manifestations of asthma. IGF-I enhances subepithelial fibrosis, airway inflammation, airway hyperresponsiveness, and airway smooth muscle hyperplasia by interacting with various inflammatory mediators and complex signaling pathways, such as intercellular adhesion molecule-1, and the hypoxia-inducible factor/vascular endothelial growth factor axis. On the other hand, IGFBP-3 decreases airway inflammation and airway hyperresponsiveness through IGFBP-3 receptor–mediated activation of caspases, which subsequently inhibits NF-κB signaling pathway. It also inhibits the IGF-I/hypoxia-inducible factor/vascular endothelial growth factor axis via IGF-I–dependent and/or IGF-I–independent mechanisms. This Translational Review summarizes the role of IGF-I and IGFBP-3 in the context of allergic airway disease, and discusses the therapeutic potential of various strategies targeting the IGF-I and IGFBP-3 signaling pathways for the management of asthma.
机译:胰岛素样生长因子(IGF)-I在哮喘的发病机理中起着关键作用,而IGF结合蛋白(IGFBP)-3则可阻断哮喘的重要生理表现。 IGF-I通过与各种炎症介质和复杂的信号通路(如细胞间粘附分子-1和缺氧诱导因子/血管内皮生长因子轴)相互作用,增强上皮下纤维化,气道炎症,气道高反应性和气道平滑肌增生。另一方面,IGFBP-3通过IGFBP-3受体介导的半胱天冬酶激活减少气道炎症和气道高反应性,从而抑制NF-κB信号通路。它还通过依赖IGF-I和/或不依赖IGF-I的机制抑制IGF-I /缺氧诱导因子/血管内皮生长因子轴。该翻译评论总结了IGF-1和IGFBP-3在过敏性气道疾病中的作用,并讨论了针对IGF-1和IGFBP-3信号通路的各种策略在治疗哮喘中的治疗潜力。

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