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本文引用的文献

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The role of endotoxin during typhoid fever and tularemia in man. I. Acquisition of tolerance to endotoxin.内毒素在人类伤寒热和兔热病中的作用。I. 对内毒素耐受性的获得。
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Virulence of Bacterium tularense. I. A study of the virulence of Bacterium tularense in mice, guinea pigs, and rabbits.土拉弗朗西斯菌的毒力。I. 土拉弗朗西斯菌在小鼠、豚鼠和兔子中毒力的研究。
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Activation of the complement system by Francisella tularensis lipopolysaccharide.土拉弗朗西斯菌脂多糖激活补体系统。
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Lipopolysaccharide-induced selective priming effects on tumor necrosis factor alpha and nitric oxide production in mouse peritoneal macrophages.脂多糖对小鼠腹腔巨噬细胞中肿瘤坏死因子α和一氧化氮产生的选择性启动作用。
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Phosphatidylinositol-anchored molecules and inducible lipopolysaccharide binding sites of human and mouse bone marrow cells.人及小鼠骨髓细胞的磷脂酰肌醇锚定分子与诱导性脂多糖结合位点
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The tularaemia vaccine.兔热病疫苗。
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Endotoxin-induced desensitization of mouse macrophages is mediated in part by nitric oxide production.内毒素诱导的小鼠巨噬细胞脱敏作用部分是由一氧化氮的产生介导的。
Infect Immun. 1995 May;63(5):1863-9. doi: 10.1128/iai.63.5.1863-1869.1995.
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Desensitization of macrophages to endotoxin effects is not correlated with a down-regulation of lipopolysaccharide-binding sites.巨噬细胞对内毒素作用的脱敏与脂多糖结合位点的下调无关。
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10
Endotoxin-induced expression of endotoxin binding sites on murine bone marrow cells.内毒素诱导小鼠骨髓细胞上内毒素结合位点的表达。
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土拉热弗朗西斯菌脂多糖无法模拟或拮抗内毒素诱导的细胞活化。

Inability of the Francisella tularensis lipopolysaccharide to mimic or to antagonize the induction of cell activation by endotoxins.

作者信息

Ancuta P, Pedron T, Girard R, Sandström G, Chaby R

机构信息

Endotoxin Group, URA-1116 of the National Center for Scientific Research, University of Paris-Sud, Orsay, France.

出版信息

Infect Immun. 1996 Jun;64(6):2041-6. doi: 10.1128/iai.64.6.2041-2046.1996.

DOI:10.1128/iai.64.6.2041-2046.1996
PMID:8675305
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC174034/
Abstract

We studied the ability of the lipopolysaccharide (LPS) extracted from a vaccine strain of Francisella tularensis (LPS-Ft) to mimic LPSs from other gram-negative bacteria for activation of various murine cell types or to antagonize the effects of other LPSs. We found that activation of macrophages for the production of tumor necrosis factor alpha and NO, of pre-B lymphocytes for the expression of surface immunoglobulins, and of bone marrow cells for the expression of LPS-binding sites was either undetectable with LPS-Ft or required concentrations 100 to 1,000 times higher than for standard LPSs. Preexposure of macrophages to LPS-Ft also failed to trigger down-regulation of tumor necrosis factor alpha (desensitization) or up-regulation of NO responses to an endotoxin challenge. In contrast to other atypical LPSs, LPS-Ft was also unable to antagonize any of the endotoxin-induced cellular responses mentioned above, suggesting that this LPS does not interact with LPS receptors.

摘要

我们研究了从土拉弗朗西斯菌疫苗株中提取的脂多糖(LPS-Ft)模拟其他革兰氏阴性菌脂多糖以激活各种小鼠细胞类型或拮抗其他脂多糖作用的能力。我们发现,LPS-Ft无法检测到对巨噬细胞产生肿瘤坏死因子α和一氧化氮、前B淋巴细胞表达表面免疫球蛋白以及骨髓细胞表达脂多糖结合位点的激活作用,或者所需浓度比标准脂多糖高100至1000倍。巨噬细胞预先暴露于LPS-Ft也未能触发肿瘤坏死因子α的下调(脱敏)或对内毒素刺激的一氧化氮反应上调。与其他非典型脂多糖不同,LPS-Ft也无法拮抗上述任何内毒素诱导的细胞反应,这表明这种脂多糖不与脂多糖受体相互作用。