首页> 外文OA文献 >Upregulation of Intercellular Adhesion Molecule 1 and Proinflammatory Cytokines by the Major Surface Proteins of Treponema maltophilum and Treponema lecithinolyticum, the Phylogenetic Group IV Oral Spirochetes Associated with Periodontitis and Endodontic Infections
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Upregulation of Intercellular Adhesion Molecule 1 and Proinflammatory Cytokines by the Major Surface Proteins of Treponema maltophilum and Treponema lecithinolyticum, the Phylogenetic Group IV Oral Spirochetes Associated with Periodontitis and Endodontic Infections

机译:麦芽螺旋体和解脂螺旋体,系统发育IV型口腔螺旋体与牙周炎和牙髓感染相关的主要表面蛋白上调细胞间粘附分子1和促炎细胞因子

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摘要

Treponema maltophilum and Treponema lecithinolyticum belong to the group IV oral spirochetes and are associated with endodontic infections, as well as periodontitis. Recently, the genes encoding the major surface proteins (Msps) of these bacteria (MspA and MspTL, respectively) were cloned and sequenced. The amino acid sequences of these proteins showed significant similarity. In this study we analyzed the functional role of these homologous proteins in human monocytic THP-1 cells and primary cultured periodontal ligament (PDL) cells using recombinant proteins. The complete genes encoding MspA and MspTL without the signal sequence were cloned into Escherichia coli by using the expression vector pQE-30. Fusion proteins tagged with N-terminal hexahistidine (recombinant MspA [rMspA] and rMspTL) were obtained, and any possible contamination of the recombinant proteins with E. coli endotoxin was removed by using polymyxin B-agarose. Flow cytometry showed that rMspA and rMspTL upregulated the expression of intercellular adhesion molecule 1 (ICAM-1) in both THP-1 and PDL cells. Expression of proinflammatory cytokines, such as interleukin-6 (IL-6) and IL-8, was also induced significantly in both cell types by the Msps, as determined by reverse transcription-PCR and an enzyme-linked immunosorbent assay, whereas IL-1β synthesis could be detected only in the THP-1 cells. The upregulation of ICAM-1, IL-6, and IL-8 was completely inhibited by pretreating the cells with an NF-κB activation inhibitor, l-1-tosylamido-2-phenylethyl chloromethyl ketone. This suggests involvement of NF-κB activation. The increased ICAM-1 and IL-8 expression in the THP-1 cells obtained with rMsps was not inhibited in the presence of the IL-1 receptor antagonist (IL-1ra), a natural inhibitor of IL-1. Our results show that the Msps of the group IV oral spirochetes may play an important role in amplifying the local immune response by continuous inflammatory cell recruitment and retention at an infection site by stimulation of expression of ICAM-1 and proinflammatory cytokines.
机译:麦芽螺旋体和解脂性螺旋体属于第四类口服螺旋体,与牙髓感染和牙周炎有关。最近,克隆了编码这些细菌主要表面蛋白(Msps)(分别为MspA和MspTL)的基因并进行了测序。这些蛋白质的氨基酸序列显示出显着的相似性。在这项研究中,我们分析了这些同源蛋白在人单核THP-1细胞和原代培养的牙周膜(PDL)细胞中的功能,并使用了重组蛋白。使用表达载体pQE-30将编码无信号序列的MspA和MspTL的完整基因克隆到大肠杆菌中。获得了标记有N端六组氨酸的融合蛋白(重组MspA [rMspA]和rMspTL),并使用多粘菌素B-琼脂糖去除了重组蛋白被大肠杆菌内毒素污染的可能性。流式细胞仪显示rMspA和rMspTL上调THP-1和PDL细胞中细胞间粘附分子1(ICAM-1)的表达。通过逆转录PCR和酶联免疫吸附试验确定,Msps在两种细胞类型中均显着诱导促炎细胞因子(如白介素6(IL-6)和IL-8)的表达,而IL- 1β合成只能在THP-1细胞中检测到。通过用NF-κB活化抑制剂1--1-甲苯磺酰氨基-2-苯基乙基氯甲基酮预处理细胞,可以完全抑制ICAM-1,IL-6和IL-8的上调。这暗示了NF-κB活化的参与。在存在IL-1天然抑制剂IL-1受体拮抗剂(IL-1ra)的情况下,用rMsps获得的THP-1细胞中ICAM-1和IL-8表达的增加并未受到抑制。我们的结果表明,IV组口服螺旋体的Msps可能通过刺激ICAM-1和促炎性细胞因子的表达,通过持续的炎症细胞募集和滞留在感染部位而在放大局部免疫应答中发挥重要作用。

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