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脑膜炎奈瑟菌诱导人内皮组织因子表达:细菌杀伤及黏附于内皮的影响

Induction of human endothelial tissue factor expression by Neisseria meningitidis: the influence of bacterial killing and adherence to the endothelium.

作者信息

Heyderman R S, Klein N J, Daramola O A, Hammerschmidt S, Frosch M, Robertson B D, Levin M, Ison C A

机构信息

Paediatric Infectious Diseases Unit, Imperial College School of Medicine at St Mary's, London, U.K.

出版信息

Microb Pathog. 1997 May;22(5):265-74. doi: 10.1006/mpat.1996.0112.

Abstract

Tissue factor (TF), a small membrane bound high affinity receptor for factor VII, has an important procoagulant role in the haemostatic dysfunction associated with severe sepsis. Using an in vitro model of human endothelial TF expression, defined strains of Neisseria meningitidis were found to upregulate endothelial cell procoagulant activity (PCA) in a dose dependent manner. This TF response was detected with as little as 10(4) cfu/ml and reached similar levels to those seen with high concentrations of purified endotoxin (> 1 ng/ml). Treatment of N. meningitidis with either adult donor immune serum, penicillin or gentamicin failed to enhance this PCA. Limulus amoebocyte lysate assay of lipopolysaccharide in bacterial culture filtrates together with polymyxin B inhibition experiments suggest that endotoxin is largely responsible for endothelial TF induction by N. meningitidis. Incubation of endothelial cells with N. meningitidis B1940 and B1940 siaD- (an eight-fold more adherent unencapsulated isogenic strain), revealed a significantly greater TF response to B1940 siaD- (P < 0.01). In conclusion, bacterial adhesion to the vessel wall and therefore local levels of endotoxin may be important determinants of the endothelial procoagulant response to N. meningitidis and the consequent coagulopathy commonly associated with the disease.

摘要

组织因子(TF)是因子VII的一种小的膜结合高亲和力受体,在与严重脓毒症相关的止血功能障碍中具有重要的促凝血作用。利用人内皮细胞TF表达的体外模型,发现特定菌株的脑膜炎奈瑟菌能以剂量依赖方式上调内皮细胞促凝血活性(PCA)。这种TF反应在低至10⁴ cfu/ml时即可检测到,且达到与高浓度纯化内毒素(>1 ng/ml)时相似的水平。用成人供体免疫血清、青霉素或庆大霉素处理脑膜炎奈瑟菌均不能增强这种PCA。对细菌培养滤液中的脂多糖进行鲎试剂检测以及多粘菌素B抑制实验表明,内毒素在很大程度上介导了脑膜炎奈瑟菌诱导的内皮细胞TF表达。将内皮细胞与脑膜炎奈瑟菌B1940及B1940 siaD⁻(一种黏附能力强八倍的无荚膜同基因菌株)共同孵育,结果显示对B1940 siaD⁻的TF反应显著更强(P<0.01)。总之,细菌对血管壁的黏附以及由此产生的局部内毒素水平可能是内皮细胞对脑膜炎奈瑟菌促凝血反应以及该疾病常见的凝血功能障碍的重要决定因素。

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