首页> 美国卫生研究院文献>The Journal of Experimental Medicine >A novel 80-kD cell surface structure identifies human circulating lymphocytes with natural killer activity
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A novel 80-kD cell surface structure identifies human circulating lymphocytes with natural killer activity

机译:一种新型的80 kD细胞表面结构可识别具有自然杀伤活性的人循环淋巴细胞

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摘要

Human lymphocytes with natural killer (NK) activity, including most activated gamma/delta+ T lymphocytes, recognize and lyse tumor target cells without requiring recognition of major histocompatibility complex antigen. However, unlike gamma/delta+ T lymphocytes, NK cells do not express CD3/T cell receptor (TCR) molecules, and the receptors involved in cell-mediated cytotoxicity are unknown. To further delineate circulating NK cells, we developed monoclonal antibodies (mAbs) against the human NK leukemia YT2C2. We report the isolation of a mAb termed BY55, recognizing at the cell surface a novel 80-kD protein with restricted expression. In addition to the immunizing cell line, this mAb binds to circulating NK cells, gamma/delta+ cells, and a minor subset of alpha/beta+ T lymphocytes. Expression of the BY55 mAb- reactive epitope/molecule is regulated by activation, as short-term culture of peripheral blood lymphocytes (PBL) with phorbol ester induced its downmodulation. Furthermore, BY55 mAb reactivity was found neither with the NK nor with the TCR alpha/beta+ gamma/delta+ clones tested. Biochemical studies as well as phenotypic analysis revealed that this structure is different from all previously identified molecules on the lymphocyte cell surface. Interestingly, we found that BY55+ cells exert most NK activity obtained with fresh circulating lymphocytes. We report that within fresh E rosette-positive PBL only a subset of the CD16+, CD56+, and CD57+ cells coexpressed BY55 molecule, indicating that BY55 mAb defines a unique subset mediating NK activity of circulating PBL.
机译:具有自然杀伤(NK)活性的人类淋巴细胞,包括大多数活化的γ/δ+ T淋巴细胞,可以识别并裂解肿瘤靶细胞,而无需识别主要的组织相容性复合抗原。但是,与γ/δ+ T淋巴细胞不同,NK细胞不表达CD3 / T细胞受体(TCR)分子,并且参与细胞介导的细胞毒性的受体尚不清楚。为了进一步描述循环的NK细胞,我们开发了针对人NK白血病YT2C2的单克隆抗体(mAb)。我们报告了一个称为BY55的mAb的分离,它在细胞表面识别了表达受限的新型80-kD蛋白。除免疫细胞系外,该mAb还与循环的NK细胞,γ/δ+细胞和一小部分α/β+ T淋巴细胞结合。 BY55 mAb反应性抗原决定簇/分子的表达受激活调节,因为佛波酯的外周血淋巴细胞(PBL)短期培养可诱导其下调。此外,在测试的NK和TCR alpha / beta + gamma / delta +克隆中均未发现BY55 mAb反应性。生化研究和表型分析表明,这种结构不同于淋巴细胞细胞表面上所有先前鉴定的分子。有趣的是,我们发现BY55 +细胞发挥了新鲜循环淋巴细胞获得的大部分NK活性。我们报告说,在新鲜的E莲座丛阳性PBL中,只有CD16 +,CD56 +和CD57 +细胞的一个亚群共表达BY55分子,这表明BY55 mAb定义了介导循环PBL NK活性的独特亚群。

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