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伯氏疏螺旋体外膜脂蛋白OspA和OspB具有B细胞促有丝分裂和细胞因子刺激特性。

Borrelia burgdorferi outer surface lipoproteins OspA and OspB possess B-cell mitogenic and cytokine-stimulatory properties.

作者信息

Ma Y, Weis J J

机构信息

Department of Pathology, University of Utah School of Medicine, Salt Lake City 84132.

出版信息

Infect Immun. 1993 Sep;61(9):3843-53. doi: 10.1128/iai.61.9.3843-3853.1993.

Abstract

Sonicated Borrelia burgdorferi was previously reported to possess both B-cell mitogenic and interleukin-6 (IL-6) stimulatory activities. In this report, two outer surface lipoproteins, OspA and OspB, were purified from B. burgdorferi and assessed for the presence of these functions. OspA was purified from two strains, an OspB-deficient variant of HB19 and N40, while OspB was purified from the N40 strain. All lipoprotein preparations were free of endotoxin contamination, and polymyxin B failed to inhibit responses, indicating that media contamination was not contributing to biological assays. All three preparations were able to stimulate proliferation of mononuclear cells from naive C3H/HeJ and BALB/c mice. Depletion experiments indicated that the responding cells were B lymphocytes and not T lymphocytes. Purified OspA and OspB stimulated immunoglobulin M production by splenocyte cultures from naive mice, a property also previously attributed to sonicated B. burgdorferi. OspA and OspB also stimulated the production of IL-6 and tumor necrosis factor alpha by bone marrow-derived macrophages from BALB/c and C3H/HeJ mice. Cytokine production was enhanced by the presence of gamma interferon in the cultures, indicating that the magnitude of responses to these lipoproteins may be modulated by cytokines in the microenvironment of infected tissues. Human endothelial cells produced IL-6 when incubated with OspA and OspB, indicating that non-hematopoietic lineage cells can respond to the lipoproteins. Purified OspA and OspB had approximately equal activity, with responses detected in the range of 10 ng of lipoprotein per ml to 1 microgram of lipoprotein per ml. Comparison with published dose responses for lipoproteins purified from Escherichia coli indicates that OspA and OspB purified from B. burgdorferi are much more potent. The high potency of the B. burgdorferi lipoproteins and the ability of the spirochete to invade tissues and persist argue that they could be important in the localized events contributing to the pathology of Lyme disease.

摘要

先前有报道称,经超声处理的伯氏疏螺旋体具有B细胞促有丝分裂活性和白细胞介素-6(IL-6)刺激活性。在本报告中,从伯氏疏螺旋体中纯化出两种外表面脂蛋白,即OspA和OspB,并对其是否具有这些功能进行了评估。OspA是从两种菌株中纯化得到的,分别是HB19的OspB缺陷变体和N40,而OspB是从N40菌株中纯化得到的。所有脂蛋白制剂均无内毒素污染,多粘菌素B未能抑制反应,这表明培养基污染并非生物测定结果的原因。所有三种制剂均能刺激来自未接触过抗原的C3H/HeJ和BALB/c小鼠的单核细胞增殖。去除实验表明,反应细胞是B淋巴细胞而非T淋巴细胞。纯化的OspA和OspB刺激了来自未接触过抗原的小鼠脾细胞培养物中免疫球蛋白M的产生,这一特性先前也归因于经超声处理的伯氏疏螺旋体。OspA和OspB还刺激了来自BALB/c和C3H/HeJ小鼠的骨髓来源巨噬细胞产生IL-6和肿瘤坏死因子α。培养物中γ干扰素的存在增强了细胞因子的产生,这表明对这些脂蛋白的反应强度可能受到感染组织微环境中细胞因子的调节。人内皮细胞在与OspA和OspB孵育时会产生IL-6,这表明非造血谱系细胞也能对这些脂蛋白产生反应。纯化的OspA和OspB具有大致相同的活性,在每毫升10纳克脂蛋白至每毫升1微克脂蛋白的范围内均可检测到反应。与从大肠杆菌中纯化的脂蛋白的已发表剂量反应进行比较表明,从伯氏疏螺旋体中纯化的OspA和OspB活性更强。伯氏疏螺旋体脂蛋白的高效性以及该螺旋体侵入组织并持续存在的能力表明,它们可能在导致莱姆病病理的局部事件中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/036f/281085/f60f84802a15/iai00021-0276-a.jpg

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