通过减少拉伸引起的肺上皮细胞损伤,阻断奈德基化可减轻呼吸机诱发的肺损伤

IF 5.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY Biochemical pharmacology Pub Date : 2024-09-13 DOI:10.1016/j.bcp.2024.116533
Tzu-Hsiung Huang , Chieh-Mo Lin , Chin-Kuo Lin , Shun-Fu Chang , Chung-Sheng Shi
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引用次数: 0

摘要

呼吸机诱发的肺损伤是机械通气患者的一种严重并发症。神经前体细胞表达的发育下调8(NEDD8)共轭的翻译后修饰--Neddylation调节着多种生物功能。然而,它在呼吸机诱导的肺损伤中的参与和治疗意义仍不清楚。因此,本研究旨在检测体内高潮气量通气(HTV)小鼠和体外循环拉伸(CS)刺激的人肺泡上皮细胞中活化的 Neddylation 的动力学和贡献以及 Neddylation 抑制的影响。NEDD8-激活酶(NAE)催化亚基泛素连接酶3(UBA3)的neddylation和表达在高潮气量通气小鼠中呈时间依赖性上调。此外,NAE抑制剂MLN4924大大减轻了HTV通气引起的急性肺损伤,表现为炎症和氧化应激的减少。此外,MLN4924 还能有效减少 Ly6Chigh 单核细胞和中性粒细胞分泌的炎性细胞因子,从而降低内皮通透性。此外,我们的研究还揭示了肺泡上皮细胞 CS 过程中 neddylation 通路、氧化应激和细胞凋亡的上调。然而,通过 MLN4924 或敲除 UBA3 阻断 neddylation 可抑制这种上调。总之,抑制 neddylation 可防止 CS 诱导的肺泡上皮细胞损伤,从而减轻 HTV 诱导的急性肺损伤。这表明,neddylation 通路在呼吸机诱导的肺损伤进展中起着关键作用。这些发现可能为治疗呼吸机诱导的肺损伤提供了新的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The blockade of neddylation alleviates ventilator-induced lung injury by reducing stretch-induced damage to pulmonary epithelial cells

Ventilator-induced lung injury is a serious complication in mechanically ventilated patients. Neddylation, the post-translational modification of neural precursor cell-expressed developmentally down-regulated 8 (NEDD8) conjugation, regulates numerous biological functions. However, its involvement and therapeutic significance in ventilator-induced lung injury remains unknown. Therefore, this study aimed to examine the kinetics and contribution of activated neddylation and the impact of neddylation inhibition in mice subjected to high tidal volume (HTV) ventilation in vivo and human pulmonary alveolar epithelial cells stimulated through cyclic stretching (CS) in vitro. The neddylation and expression of ubiquitin conjugating enzyme 3 (UBA3), a NEDD8-activating enzyme (NAE) catalytic subunit, were time-dependently upregulated in HTV-ventilated mice. Additionally, the NAE inhibitor MLN4924 considerably attenuated acute lung injury induced by HTV ventilation, manifesting as reduced inflammation and oxidative stress. Furthermore, MLN4924 effectively reduced the secretion of inflammatory cytokines from Ly6Chigh monocytes and neutrophils, subsequently decreasing endothelial permeability. Moreover, our study revealed an upregulation of the neddylation pathway, oxidative stress, and apoptosis during CS of alveolar epithelial cells. However, blockade of neddylation via MLN4924 or through UBA3 knockdown suppressed this upregulation. Overall, the inhibition of neddylation may alleviate HTV-induced acute lung injury by preventing CS-induced damage to alveolar epithelial cells. This indicates that the neddylation pathway plays a critical role in the progression of ventilator-induced lung injury. These findings may provide a new therapeutic target for treating ventilator-induced lung injury.

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来源期刊
Biochemical pharmacology
Biochemical pharmacology 医学-药学
CiteScore
10.30
自引率
1.70%
发文量
420
审稿时长
17 days
期刊介绍: Biochemical Pharmacology publishes original research findings, Commentaries and review articles related to the elucidation of cellular and tissue function(s) at the biochemical and molecular levels, the modification of cellular phenotype(s) by genetic, transcriptional/translational or drug/compound-induced modifications, as well as the pharmacodynamics and pharmacokinetics of xenobiotics and drugs, the latter including both small molecules and biologics. The journal''s target audience includes scientists engaged in the identification and study of the mechanisms of action of xenobiotics, biologics and drugs and in the drug discovery and development process. All areas of cellular biology and cellular, tissue/organ and whole animal pharmacology fall within the scope of the journal. Drug classes covered include anti-infectives, anti-inflammatory agents, chemotherapeutics, cardiovascular, endocrinological, immunological, metabolic, neurological and psychiatric drugs, as well as research on drug metabolism and kinetics. While medicinal chemistry is a topic of complimentary interest, manuscripts in this area must contain sufficient biological data to characterize pharmacologically the compounds reported. Submissions describing work focused predominately on chemical synthesis and molecular modeling will not be considered for review. While particular emphasis is placed on reporting the results of molecular and biochemical studies, research involving the use of tissue and animal models of human pathophysiology and toxicology is of interest to the extent that it helps define drug mechanisms of action, safety and efficacy.
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