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表达γ/δ T细胞受体的人胸腺细胞。

Human thymocytes expressing gamma/delta T-cell receptors.

作者信息

Mingari M C, Varese P, Bottino C, Tambussi G, Moretta L

机构信息

Istituto Nazionale per la Ricerca sul Cancro, Genoa, Italy.

出版信息

Int J Cancer Suppl. 1989;4:39-42. doi: 10.1002/ijc.2910440711.

Abstract

Expression of T-cell receptors of gamma/delta type characterizes a small subset of peripheral T lymphocytes which is homogeneously composed of cytolytic cells and, in most instances, lack CD4 and CD8 differentiation antigens. By the use of anti-TCR gamma/delta MAbs it is possible to identify two distinct subsets of TCR gamma/delta+ cells that are characterized by a C gamma 1 or C gamma 2-encoded forms of gamma-chain, respectively. While the BB3 MAb-reactive (C gamma 1 encoded) cell subset is prevalent in peripheral blood (PB), these cells represent less than 10% in TCR gamma/delta+ thymocyte populations. In thymus, the majority of cells was found to react with delta-TCSI (or A13) MAbs. Culture of CD4-8- thymocytes (highly enriched in TCR gamma/delta+ cells) in IL-2 resulted in the de novo expression of CD8 surface antigen and of non MHC-restricted cytolytic activity. Cloning of CD4-8- thymocytes resulted, for the most part, in CD3+ TCR gamma/delta+ cells. Moreover, the majority of clones expressed the unusual delta-TCSI+ CD8+ phenotype and lysed the NK-sensitive K562 target cells. Analysis of the immunoprecipitated TCR molecules showed the existence of the (rare) heavy (55 kDa) form of gamma-chain. A redirected killing assay using murine P815 target cells and appropriate "stimulatory" antibodies was further employed for functional analysis of thymus-derived TCR gamma/delta+ clones. While anti-CD3 MAbs efficiently triggered the cytolytic activity of all clones irrespective of their phenotype, MAbs directed to TCR gamma/delta induced efficient lysis only of BB3+ or delta-TCSI+CD8 clones, but not of delta-TCSI+ CD8+ clones.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

γ/δ型T细胞受体的表达是外周T淋巴细胞一小亚群的特征,该亚群由溶细胞性细胞均匀组成,且在大多数情况下缺乏CD4和CD8分化抗原。通过使用抗TCRγ/δ单克隆抗体,可以识别出TCRγ/δ+细胞的两个不同亚群,它们分别以γ链的Cγ1或Cγ2编码形式为特征。虽然BB3单克隆抗体反应性(Cγ1编码)细胞亚群在外周血(PB)中占优势,但这些细胞在TCRγ/δ+胸腺细胞群体中所占比例不到10%。在胸腺中,发现大多数细胞与δ-TCSI(或A13)单克隆抗体反应。在白细胞介素-2中培养CD4-8-胸腺细胞(高度富集TCRγ/δ+细胞)导致CD8表面抗原和非MHC限制性溶细胞活性的从头表达。CD4-8-胸腺细胞的克隆大多产生CD3+TCRγ/δ+细胞。此外,大多数克隆表达不寻常的δ-TCSI+CD8+表型并裂解NK敏感的K562靶细胞。对免疫沉淀的TCR分子的分析显示存在(罕见的)重链(55 kDa)形式的γ链。使用鼠P815靶细胞和适当的“刺激”抗体的重定向杀伤试验进一步用于胸腺来源的TCRγ/δ+克隆的功能分析。虽然抗CD3单克隆抗体能有效触发所有克隆的溶细胞活性,而不论其表型如何,但针对TCRγ/δ的单克隆抗体仅能有效裂解BB3+或δ-TCSI+CD8克隆,而不能裂解δ-TCSI+CD8+克隆。(摘要截短于250字)

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