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含有CpG基序的关节内局部细菌DNA可诱发关节炎。

Intra-articularly localized bacterial DNA containing CpG motifs induces arthritis.

作者信息

Deng G M, Nilsson I M, Verdrengh M, Collins L V, Tarkowski A

机构信息

Department of Rheumatology, University of Göteborg, Sweden.

出版信息

Nat Med. 1999 Jun;5(6):702-5. doi: 10.1038/9554.

Abstract

Unmethylated CpG motifs are often found in bacterial DNA, and exert immunostimulatory effects on hematopoietic cells. Bacteria produce severe joint inflammation in septic and reactive arthritides; bacterial DNA may be involved in this process. We injected bacterial DNA originating from Escherichia coli and Staphylococcus aureus and oligonucleotides containing CpG directly into the knee joints of mice of different strains. Arthritis was seen by histopathology within 2 hours and lasted for at least 14 days. Unmethylated CpG motifs were responsible for this induction of arthritis, as oligonucleotides containing these motifs produced the arthritis. The arthritis was characterized by an influx of monocytic, Mac-1+ cells and by a lack of T lymphocytes. Depletion of monocytes resulted in abrogation of the synovial inflammation. Tumor necrosis factor (TNF)-alpha, a cytokine produced by cells of the monocyte/macrophage lineage, is an important mediator of this disease, as expression of mRNA for TNF-alpha was evident in the inflamed joints, and the CpG-mediated inflammation was abrogated in mice genetically unable to produce this cytokine. These findings demonstrate that bacterial DNA containing unmethylated CpG motifs induces arthritis, and indicate an important pathogenic role for bacterial DNA in septic arthritis.

摘要

未甲基化的CpG基序常见于细菌DNA中,并对造血细胞产生免疫刺激作用。细菌在脓毒性关节炎和反应性关节炎中引发严重的关节炎症;细菌DNA可能参与了这一过程。我们将源自大肠杆菌和金黄色葡萄球菌的细菌DNA以及含CpG的寡核苷酸直接注射到不同品系小鼠的膝关节中。2小时内通过组织病理学观察到关节炎,且持续至少14天。未甲基化的CpG基序是这种关节炎诱导的原因,因为含有这些基序的寡核苷酸会引发关节炎。这种关节炎的特征是单核细胞、Mac-1+细胞流入,且缺乏T淋巴细胞。单核细胞的耗竭导致滑膜炎症消失。肿瘤坏死因子(TNF)-α是单核细胞/巨噬细胞系细胞产生的一种细胞因子,是这种疾病的重要介质,因为在发炎关节中TNF-α的mRNA表达明显,且在基因上无法产生这种细胞因子的小鼠中,CpG介导的炎症消失。这些发现表明,含有未甲基化CpG基序的细菌DNA可诱导关节炎,并表明细菌DNA在脓毒性关节炎中具有重要的致病作用。

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