Ancuta P, Pedron T, Girard R, Sandström G, Chaby R
Endotoxin Group, URA-1116 of the National Center for Scientific Research, University of Paris-Sud, Orsay, France.
Infect Immun. 1996 Jun;64(6):2041-6. doi: 10.1128/iai.64.6.2041-2046.1996.
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.
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。