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细菌超抗原葡萄球菌肠毒素B在体外培养过程中刺激淋巴细胞的运动能力。

The bacterial superantigen Staphylococcal enterotoxin B stimulates lymphocyte locomotor capacity during culture in vitro.

作者信息

Newman I, Wilkinson P C

机构信息

Department of Immunology, University of Glasgow, UK.

出版信息

Immunology. 1996 Mar;87(3):428-33. doi: 10.1046/j.1365-2567.1996.491565.x.

Abstract

The bacterial superantigen Staphylococcal enterotoxin B (SEB) was investigated for its effects on lymphocyte locomotion in vitro. Culture of peripheral blood mononuclear cells (PBMC) for 24-72 hr in SEB (1-100 micrograms/ml) increased the proportion of lymphocytes in locomotor (polarized) morphology and capable of invading collagen gels, to the same extent as the established locomotor activator, anti-CD3 (alpha-CD3), though the conventional antigen, tetanus toxoid was ineffective. The cells responding to SEB were predominantly T cells. SEB had no effect on lymphocyte locomotion in short-term (45 min) assays, thus its effect is to stimulate growth-related locomotor capacity and it does not act as a chemoattractant. During culture of PBMC in SEB, the chemokines interleukin-8 (IL-8) and macrophage chemotactic protein-1 (MCP-1) were released into the culture medium. The presence of anti-IL-8, but not of anti-MCP-1, either during culture or added to SEB culture supernatants and tested in short-term assays, inhibited the development of polarization suggesting that IL-8, which is a lymphocyte chemoattractant, also plays a key role in SEB-induced locomotor activation. Among SEB-activated lymphocytes, CD45RO+CD45RA- lymphocytes showed enhanced locomotor responses, but a relation was not found between locomotor activity and the presence of cell surface CD69.

摘要

研究了细菌超抗原葡萄球菌肠毒素B(SEB)对体外淋巴细胞运动的影响。外周血单个核细胞(PBMC)在SEB(1 - 100微克/毫升)中培养24 - 72小时,可增加呈运动(极化)形态且能够侵入胶原凝胶的淋巴细胞比例,其程度与既定的运动激活剂抗CD3(α-CD3)相同,而传统抗原破伤风类毒素则无效。对SEB作出反应的细胞主要是T细胞。在短期(45分钟)试验中,SEB对淋巴细胞运动没有影响,因此其作用是刺激与生长相关的运动能力,而不是作为趋化因子。在PBMC于SEB中培养期间,趋化因子白细胞介素-8(IL-8)和巨噬细胞趋化蛋白-1(MCP-1)被释放到培养基中。在培养期间或添加到SEB培养上清液中并在短期试验中进行测试时,抗IL-8(而非抗MCP-1)的存在抑制了极化的发展,这表明作为淋巴细胞趋化因子的IL-8在SEB诱导的运动激活中也起关键作用。在SEB激活的淋巴细胞中,CD45RO + CD45RA-淋巴细胞表现出增强的运动反应,但未发现运动活性与细胞表面CD69的存在之间存在关联。

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