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血管内皮生长因子A促成多杀性巴氏杆菌感染诱导的哺乳动物呼吸道上皮通透性增加。

Vascular Endothelial Growth Factor A Contributes to Increased Mammalian Respiratory Epithelial Permeability Induced by Pasteurella multocida Infection.

作者信息

Lin Lin, Yang Jie, Zhang Dajun, Lv Qingjie, Wang Fei, Liu Peng, Wang Mixue, Shi Congcong, Huang Xi, Liang Wan, Tan Chen, Wang Xiangru, Chen Huanchun, Wilson Brenda A, Wu Bin, Peng Zhong

机构信息

State Key Laboratory of Agricultural Microbiology, The Cooperative Innovation Center for Sustainable Pig Production, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, China.

Department of Microbiology, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.

出版信息

Microbiol Spectr. 2023 Mar 14;11(2):e0455422. doi: 10.1128/spectrum.04554-22.

Abstract

Pasteurella multocida infection can cause significant zoonotic respiratory problems in both humans and animals, but little is known about the mechanisms used by P. multocida to invade and cross the mammalian respiratory barrier. In this study, we investigated the influence of P. multocida infection on the dysfunction of the respiratory epithelial barrier. tests in mouse infection models demonstrated that P. multocida infection significantly increased epithelial permeability and increased the expression of vascular endothelial growth factor A (VEGFA) and endothelial nitric oxide synthase (eNOS) in murine tracheae and lungs. In murine lung epithelial cell (MLE-12) models, P. multocida infection decreased the expression of tight junctions (ZO-1) and adherens junctions (β-catenin and E-cadherin) proteins but induced the activation of hypoxia-inducible factor 1α (HIF-1α) and VEGFA signaling. When the expression of HIF-1α is suppressed, the induction of VEGFA and ZO-1 expression by P. multocida infection is decreased. We also found that intervention of HIF-1α and VEGFA signaling affected infection outcomes caused by respiratory bacteria in mouse models. Most importantly, we demonstrate that P. multocida infection increases the permeability of human respiratory epithelial cells and that this process is associated with the activation of HIF-1α and VEGFA signaling and likely contributes to the pathogenesis of P. multocida infection in humans. The mammalian respiratory epithelium forms the first line of defense against infections with P. multocida, an important zoonotic respiratory pathogen. In this study, we found that P. multocida infection increased respiratory epithelial permeability and promoted the induction of the HIF-1α-VEGFA axis in both mouse and murine cell models. Similar findings were also demonstrated in human respiratory epithelial cells. The results from this study provide important knowledge about the pathogenesis of P. multocida causing infections in both animals and humans.

摘要

多杀巴斯德菌感染可在人和动物中引发严重的人畜共患呼吸道问题,但对于多杀巴斯德菌侵入并穿越哺乳动物呼吸道屏障所采用的机制,人们了解甚少。在本研究中,我们调查了多杀巴斯德菌感染对呼吸道上皮屏障功能障碍的影响。小鼠感染模型试验表明,多杀巴斯德菌感染显著增加上皮通透性,并增加小鼠气管和肺部血管内皮生长因子A(VEGFA)和内皮型一氧化氮合酶(eNOS)的表达。在小鼠肺上皮细胞(MLE-12)模型中,多杀巴斯德菌感染降低了紧密连接(ZO-1)和黏附连接(β-连环蛋白和E-钙黏蛋白)蛋白的表达,但诱导了缺氧诱导因子1α(HIF-1α)和VEGFA信号通路的激活。当HIF-1α的表达受到抑制时,多杀巴斯德菌感染对VEGFA和ZO-1表达的诱导作用减弱。我们还发现,干预HIF-1α和VEGFA信号通路会影响小鼠模型中呼吸道细菌引起的感染结果。最重要的是,我们证明多杀巴斯德菌感染会增加人呼吸道上皮细胞的通透性,且这一过程与HIF-1α和VEGFA信号通路的激活有关,可能促成了多杀巴斯德菌在人类中的感染发病机制。哺乳动物呼吸道上皮构成了抵御重要人畜共患呼吸道病原体多杀巴斯德菌感染的第一道防线。在本研究中,我们发现多杀巴斯德菌感染在小鼠和小鼠细胞模型中均增加了呼吸道上皮通透性,并促进了HIF-1α-VEGFA轴的诱导。在人呼吸道上皮细胞中也得到了类似的结果。本研究结果为多杀巴斯德菌在动物和人类中引起感染的发病机制提供了重要知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3477/10101004/031b6922e254/spectrum.04554-22-f001.jpg

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