Tohme Z N, Amar S, Van Dyke T E
Goldman School of Dental Medicine, Boston University, Boston, Massachusetts 02118, USA.
Infect Immun. 1999 Jul;67(7):3215-20. doi: 10.1128/IAI.67.7.3215-3220.1999.
Bacterial endotoxin (lipopolysaccharide [LPS]), a glycolipid found in the outer membranes of gram-negative bacteria, induces the secretion of proinflammatory cytokines such as tumor necrosis factor alpha (TNF-alpha), interleukin-1 (IL-1), and IL-6 by monocytes/macrophages. The secretion of these biologically active compounds leads to multiple pathological conditions, such as septic shock. There is substantial evidence that chronic exposure to LPS mediates, at least in part, the tissue destruction associated with gram-negative infection. CD14, a 55-kDa protein, has been identified as an LPS receptor. In conjunction with a serum protein, LPS binding protein (LBP), LPS-CD14 interactions mediate many LPS functions in the inflammatory response. However, CD14 lacks a cytoplasmic domain, or any known signal transduction sequence motif, suggesting the existence of another cell surface domain capable of transducing signals. In this paper, we report a second, CD14-independent LPS binding site, which, based on biological activity, appears to be a functional LPS receptor. Cross-linking experiments were performed to identify LPS binding sites. Two molecules were identified: a 55-kDa protein (CD14) and a second, 78-kDa band. Sequencing of the 78-kDa protein by mass spectroscopic analysis revealed 100% homology with moesin (membrane-organizing extension spike protein). Antibody to CD14 induced partial blocking of the LPS response. However, antimoesin monoclonal antibody completely blocked the LPS-induced TNF-alpha response in human monocytes, without blocking CD14 binding of LPS. Irrelevant isotype controls had no effect. Additional experiments were performed to evaluate the specificity of the antimoesin blocking. Separate experiments evaluated antimoesin effects on monocyte chemotaxis, IL-1 production in response to IL-1 stimulation, and TNF-alpha secretion in response to Staphylococcus aureus stimulation. Antimoesin blocked only LPS-mediated events. The data suggest that moesin functions as an independent LPS receptor on human monocytes. The role of moesin in transduction of CD14-mediated signals is discussed.
细菌内毒素(脂多糖[LPS])是一种存在于革兰氏阴性菌外膜中的糖脂,可诱导单核细胞/巨噬细胞分泌促炎细胞因子,如肿瘤坏死因子α(TNF-α)、白细胞介素-1(IL-1)和IL-6。这些生物活性化合物的分泌会导致多种病理状况,如脓毒性休克。有大量证据表明,长期暴露于LPS至少部分介导了与革兰氏阴性菌感染相关的组织破坏。CD14是一种55 kDa的蛋白质,已被确定为LPS受体。LPS与血清蛋白LPS结合蛋白(LBP)结合后,LPS-CD14相互作用介导了炎症反应中许多LPS的功能。然而,CD14缺乏胞质结构域或任何已知的信号转导序列基序,这表明存在另一个能够转导信号的细胞表面结构域。在本文中,我们报告了第二个不依赖CD14的LPS结合位点,基于生物学活性,它似乎是一个功能性LPS受体。进行了交联实验以鉴定LPS结合位点。鉴定出了两种分子:一种55 kDa的蛋白质(CD14)和另一条78 kDa的条带。通过质谱分析对78 kDa蛋白质进行测序,结果显示其与埃兹蛋白(膜组织伸展刺突蛋白)有100%的同源性。抗CD14抗体可部分阻断LPS反应。然而,抗埃兹蛋白单克隆抗体可完全阻断LPS诱导的人单核细胞中TNF-α反应,而不阻断LPS与CD14的结合。无关的同型对照无此作用。进行了额外的实验以评估抗埃兹蛋白阻断的特异性。单独的实验评估了抗埃兹蛋白对单核细胞趋化性、对IL-1刺激的IL-1产生以及对金黄色葡萄球菌刺激的TNF-α分泌的影响。抗埃兹蛋白仅阻断LPS介导的事件。数据表明,埃兹蛋白在人单核细胞上作为独立的LPS受体发挥作用。本文还讨论了埃兹蛋白在CD14介导信号转导中的作用。