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本文引用的文献

1
Reovirus infection in rat lungs as a model to study the pathogenesis of viral pneumonia.以大鼠肺部呼肠孤病毒感染作为研究病毒性肺炎发病机制的模型。
J Virol. 1996 Jan;70(1):541-8. doi: 10.1128/JVI.70.1.541-548.1996.
2
Chemoattractants for neutrophils in lipopolysaccharide-induced inflammatory exudate from rats are not interleukin-8 counterparts but gro-gene-product/melanoma-growth-stimulating-activity-related factors.脂多糖诱导的大鼠炎性渗出物中嗜中性粒细胞的趋化因子并非白细胞介素-8类似物,而是生长调节致癌基因产物/黑素瘤生长刺激活性相关因子。
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Pulmonary epithelial cells facilitate TNF-alpha-induced neutrophil chemotaxis. A role for cytokine networking.肺上皮细胞促进肿瘤坏死因子-α诱导的中性粒细胞趋化作用。细胞因子网络的作用。
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Endogenous IL-1 is required for neutrophil recruitment and macrophage activation during murine listeriosis.内源性白细胞介素-1是小鼠李斯特菌病中性粒细胞募集和巨噬细胞激活所必需的。
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Functional characterization of the rat chemokine KC and its importance in neutrophil recruitment in a rat model of pulmonary inflammation.大鼠趋化因子KC的功能特性及其在肺部炎症大鼠模型中性粒细胞募集过程中的重要性。
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Airway neutrophilia and chemokine mRNA expression in sulfur dioxide-induced bronchitis.二氧化硫诱导的支气管炎中气道中性粒细胞增多及趋化因子mRNA表达
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Human tumour necrosis factor: precursor structure, expression and homology to lymphotoxin.人肿瘤坏死因子:前体结构、表达及其与淋巴毒素的同源性。
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呼肠孤病毒对肺部中性粒细胞增多及炎性细胞因子基因表达的血清型依赖性诱导作用

Serotype-dependent induction of pulmonary neutrophilia and inflammatory cytokine gene expression by reovirus.

作者信息

Farone A L, Frevert C W, Farone M B, Morin M J, Fields B N, Paulauskis J D, Kobzik L

机构信息

Department of Environmental Health, Harvard School of Public Health, Boston, Massachusetts 02115, USA.

出版信息

J Virol. 1996 Oct;70(10):7079-84. doi: 10.1128/JVI.70.10.7079-7084.1996.

DOI:10.1128/JVI.70.10.7079-7084.1996
PMID:8794353
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC190759/
Abstract

Reovirus type 3 Dearing (T3D) causes a prominent neutrophil influx, substantially greater than seen with reovirus type 1 Lang (T1L) in a rat model of viral pneumonia. We sought to measure reovirus-mediated increases in chemokine mRNA expression in pulmonary cells. We found that the neutrophilia induced by T1L and T3D infection in vivo correlated directly with increased levels of chemokine mRNA expression in T3D-infected compared with those of T1IL-infected lungs. In vitro, reovirus-infected normal alveolar macrophages (AMs) and the rat AM cell line NR8383 expressed greater levels of macrophage inflammatory protein 2, KC, and tumor necrosis factor alpha mRNA. A synergism between reovirus and lipopolysaccharide was also detected for macrophage inflammatory protein 2 and KC mRNA expression. Tumor necrosis factor protein secretion was also increased to a greater extent by T3D than by T1L in primary rat AMs and the NR8383 cells. We conclude that the virus-mediated inflammatory cytokine induction suggests a role for these cytokines in the neutrophil influx observed in the rat reovirus pneumonia model.

摘要

3型迪林呼肠孤病毒(T3D)会引起显著的中性粒细胞浸润,在病毒性肺炎大鼠模型中,这种浸润程度比1型朗氏呼肠孤病毒(T1L)引起的要大得多。我们试图测量呼肠孤病毒介导的肺细胞趋化因子mRNA表达的增加。我们发现,在体内,T1L和T3D感染诱导的中性粒细胞增多与T3D感染的肺相比T1L感染的肺中趋化因子mRNA表达水平的增加直接相关。在体外,呼肠孤病毒感染的正常肺泡巨噬细胞(AM)和大鼠AM细胞系NR8383表达更高水平的巨噬细胞炎性蛋白2、KC和肿瘤坏死因子α mRNA。对于巨噬细胞炎性蛋白2和KC mRNA表达,还检测到呼肠孤病毒与脂多糖之间的协同作用。在原代大鼠AM和NR8383细胞中,T3D比T1L更能显著增加肿瘤坏死因子蛋白的分泌。我们得出结论,病毒介导的炎性细胞因子诱导表明这些细胞因子在大鼠呼肠孤病毒肺炎模型中观察到的中性粒细胞浸润中起作用。