Induction of E-Selectin by Endotoxin is Direct and not Mediated Through Intracellular or Extracellular Release of Secondary Cytokines

P. Adamson, M. Tighe, H. Paterson, J. Pearson
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引用次数: 1

Abstract

Using a fixed cell ELISA system E-selectin expression and adhesion of U937 cells were measured in both endotoxin (LPS: serotype 0111:B4) tregted and untreated cultures of human umbilical vein endothelial cells (HUVEC). Basal levels of E-selectin were unde-tectable whereas significant induction of both E-selectin and U937 cell adhesion were observed after exposure of HUVEC to LPS for 6h. The effect of LPS was serum dependent and unaffected by coincubation with neutralising antibodies to either IL-1α, IL-1β or TNFα either alone or in combination, even though each antibody was capable of neutralising the effect of exogenously added cytokine. In addition IgG fractions of neutralising anti-cytokine antibodies were purified, concentrated and microinjected into the cytosol of adherent HUVEC prior to treatment with 1 μg/ml LPS for 6 hrs. Immunofluorescence staining showed that cells microinjected with antibodies to IL-1α, IL-1β and TNFα either alone or in combination were positive for LPS-stimulated E-selectin, d...
内毒素对e -选择素的诱导是直接的,而不是通过细胞内或细胞外次生细胞因子的释放介导的
采用固定细胞ELISA系统,测定了内毒素(LPS:血清型0111:B4)处理和未处理的人脐静脉内皮细胞(HUVEC)中U937细胞e -选择素的表达和粘附性。e-选择素的基础水平无法检测到,而在LPS作用6小时后,我们观察到e-选择素和U937细胞粘附的显著诱导。LPS的作用是血清依赖的,并且不受单独或联合中和IL-1α、IL-1β或TNFα抗体的影响,尽管每种抗体都能够中和外源添加的细胞因子的作用。将中和性抗细胞因子抗体的IgG部分纯化浓缩后,用1 μg/ml LPS处理HUVEC,微注射于贴壁HUVEC细胞质中,作用6小时。免疫荧光染色显示,单独或联合注射IL-1α、IL-1β和TNFα抗体的细胞中,lps刺激的e -选择素呈阳性。
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