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The integrated stress response in pulmonary disease

机译:肺病中的综合应力反应

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The respiratory tract and its resident immune cells face daily exposure to stress, both from without and from within. Inhaled pathogens, including severe acute respiratory syndrome coronavirus 2, and toxins from pollution trigger a cellular defence system that reduces protein synthesis to minimise viral replication or the accumulation of misfolded proteins. Simultaneously, a gene expression programme enhances antioxidant and protein folding machineries in the lung. Four kinases (PERK, PKR, GCN2 and HRI) sense a diverse range of stresses to trigger this “integrated stress response”. Here we review recent advances identifying the integrated stress response as a critical pathway in the pathogenesis of pulmonary diseases, including pneumonias, thoracic malignancy, pulmonary fibrosis and pulmonary hypertension. Understanding the integrated stress response provides novel targets for the development of therapies.
机译:呼吸道和其常规免疫细胞从没有和来自内部接触到压力,都是暴露于压力。 吸入病原体,包括严重的急性呼吸综合征冠状病毒2,以及来自污染的毒素触发了一种细胞防御系统,可降低蛋白质合成以最小化病毒复制或错误折叠蛋白的积累。 同时,基因表达程序增强肺中的抗氧化剂和蛋白质折叠机械。 四个激酶(Perk,PKR,GCN2和HRI)感测多种压力,以触发这种“综合应力响应”。 在这里,我们审查了最近将综合应力响应的预付款作为肺病发病机制中的关键途径,包括肺炎,胸部恶性肿瘤,肺纤维化和肺动脉高血压。 了解综合应力响应为疗法的发展提供了新的目标。

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