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NEDD4 通过抑制 Notch1 激活来减轻光气诱导的急性肺损伤。

NEDD4 attenuates phosgene-induced acute lung injury through the inhibition of Notch1 activation.

机构信息

Center of Emergency & Intensive Care Unit, Jinshan Hospital, Fudan University, Shanghai, China.

Key Laboratory of Chemical Injury, Emergency and Critical Medicine of Shanghai Municipal Health Commission, Shanghai, China.

出版信息

J Cell Mol Med. 2022 May;26(10):2831-2840. doi: 10.1111/jcmm.17296. Epub 2022 Mar 31.

Abstract

Phosgene gas leakage can cause life-threatening acute lung injury (ALI), which is characterized by inflammation, increased vascular permeability, pulmonary oedema and oxidative stress. Although the downregulation of neuronal precursor cell-expressed developmentally downregulated 4 (NEDD4) is known to be associated with inflammation and oxidative damage, its functions in phosgene-induced ALI remain unclear. In this study, rats with phosgene-induced ALI were intravenously injected with NEDD4-overexpressing lentiviruses to determine the functions of NEDD4 in this inflammatory condition. NEDD4 expression was decreased in the lung parenchyma of phosgene-exposed control rats, whereas its expression level was high in the NEDD4-overexpressing rats. Phosgene exposure increased the wet-to-dry lung weight ratio, but NEDD4 abrogated this effect. NEDD4 overexpression attenuated phosgene-induced lung inflammation, lowering the high lung injury score (based on total protein, inflammatory cells and inflammatory factors in bronchoalveolar lavage fluid) and also reduced phosgene-induced oxidative stress and cell apoptosis. Finally, NEDD4 was found to interact with Notch1, enhancing its ubiquitination and thereby its degradation, thus attenuating the inflammatory responses to ALI. Therefore, we demonstrated that NEDD4 plays a protective role in alleviating phosgene-induced ALI, suggesting that enhancing the effect of NEDD4 may be a new approach for treating phosgene-induced ALI.

摘要

光气气体泄漏可导致危及生命的急性肺损伤(ALI),其特征为炎症、血管通透性增加、肺水肿和氧化应激。虽然神经元前体细胞表达的发育下调 4(NEDD4)的下调与炎症和氧化损伤有关,但其在光气诱导的 ALI 中的作用尚不清楚。在这项研究中,用光气诱导 ALI 的大鼠静脉注射 NEDD4 过表达慢病毒,以确定 NEDD4 在这种炎症状态下的功能。光气暴露的对照组大鼠肺实质中 NEDD4 的表达减少,而 NEDD4 过表达组大鼠中 NEDD4 的表达水平较高。光气暴露增加了肺湿重与干重的比值,但 NEDD4 减弱了这种作用。NEDD4 过表达减轻了光气诱导的肺炎症,降低了高肺损伤评分(基于支气管肺泡灌洗液中的总蛋白、炎症细胞和炎症因子),并减轻了光气诱导的氧化应激和细胞凋亡。最后,发现 NEDD4 与 Notch1 相互作用,增强其泛素化,从而使其降解,从而减轻 ALI 的炎症反应。因此,我们证明了 NEDD4 在减轻光气诱导的 ALI 中发挥保护作用,提示增强 NEDD4 的作用可能是治疗光气诱导的 ALI 的一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90be/9097839/af02b0aeb76f/JCMM-26-2831-g004.jpg

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