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p53 在支气管肺泡细胞中促进衰老从而促进慢性肺部炎症。

p53 in Bronchial Club Cells Facilitates Chronic Lung Inflammation by Promoting Senescence.

机构信息

Department of Molecular Cell Biology, The Weizmann Institute of Science, 7610001 Rehovot, Israel.

Department of Immunology, The Weizmann Institute of Science, 7610001 Rehovot, Israel.

出版信息

Cell Rep. 2018 Mar 27;22(13):3468-3479. doi: 10.1016/j.celrep.2018.03.009.

Abstract

The tumor suppressor p53 limits tumorigenesis by inducing apoptosis, cell cycle arrest, and senescence. Although p53 is known to limit inflammation during tumor development, its role in regulating chronic lung inflammation is less well understood. To elucidate the function of airway epithelial p53 in such inflammation, we subjected genetically modified mice, whose bronchial epithelial club cells lack p53, to repetitive inhalations of lipopolysaccharide (LPS), an exposure that leads to severe chronic bronchitis and airway senescence in wild-type mice. Surprisingly, the club cell p53 knockout mice exhibited reduced airway senescence and bronchitis in response to chronic LPS exposure and were significantly protected from global lung destruction. Furthermore, pharmacological elimination of senescent cells also protected wild-type mice from chronic LPS-induced bronchitis. Our results implicate p53 in induction of club-cell senescence and correlate epithelial cell senescence of chronic airway inflammation and lung destruction.

摘要

抑癌基因 p53 通过诱导细胞凋亡、细胞周期阻滞和衰老来限制肿瘤发生。尽管已知 p53 可在肿瘤发展过程中限制炎症,但它在调节慢性肺部炎症中的作用还不太清楚。为了阐明气道上皮 p53 在这种炎症中的功能,我们对支气管上皮细胞中的 club 细胞缺乏 p53 的基因修饰小鼠进行了重复的脂多糖(LPS)吸入,这种暴露会导致野生型小鼠发生严重的慢性支气管炎和气道衰老。令人惊讶的是,在慢性 LPS 暴露下,club 细胞 p53 敲除小鼠表现出的气道衰老和支气管炎减少,并且对全肺破坏有明显的保护作用。此外,药物消除衰老细胞也可保护野生型小鼠免受慢性 LPS 诱导的支气管炎。我们的结果表明 p53 参与诱导 club 细胞衰老,并将慢性气道炎症和肺破坏的上皮细胞衰老联系起来。

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