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长期培养的T细胞和自然杀伤细胞所表达的一种新型表面分子参与细胞活化。

A novel surface molecule expressed by long-term cultured T and natural killer cells is involved in cell activation.

作者信息

Ferrini S, Cantoni C, Ciccone E, Biassoni R, Prigione I, Bottino C, Venzano P, Moretta L

机构信息

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

出版信息

Eur J Immunol. 1991 Sep;21(9):1981-7. doi: 10.1002/eji.1830210903.

Abstract

Two monoclonal antibodies (mAb), termed ED6 and LD6, were obtained by immunizing mice with cytotoxic T cell lines expressing the T cell receptor (TcR) gamma/delta. These mAb were selected according to their ability to trigger the cytolytic program of the immunizing cell lines in a redirected killing assay. Both mAb recognized molecule(s) expressed on the surface of most long-term cultured TcR gamma/delta +, TcR alpha/beta + and CD3-CD16+ lymphocytes, while it was absent on resting peripheral blood lymphocytes. In addition both mAb reacted with neoplastic B cell lines, Epstein-Barr virus-transformed B cell lines, small cell lung cancer and glioma cell lines, while no surface reactivity was detected on ovarian, breast, colon and non-small cell lung cancer lines. The functional activity of these mAb was studied by two cytolytic assays. Both mAb were able to trigger the cytolytic program of CD3+TcR gamma/delta + polyclonal cell lines and of a CD3-CD16+ NK cell clone against the murine mastocytoma target cell line P815 (Fc receptor+) in a 4-h 51Cr-release assay. In addition, ED6 and LD6 hybridomas were lysed by TcR gamma/delta + effector cells while other hybridomas (obtained from the same fusion) were not lysed. ED6 and LD6 mAb (in the presence of submitogenic doses of the phorbol 12-myristate 13-acetate) also induced the secretion of interleukin 2 by ED6/LD6+ T cell clones expressing TcR gamma/delta or alpha/beta. mAb-induced surface antigen modulation experiments showed that the antigenic determinant recognized by ED6 and LD6 co-modulated, thus indicating that the two mAb probably recognize the same or closely associated molecules. The molecular characteristics of the antigen recognized by the mAb were investigated by Western blot analysis. The LD6 mAb recognized a major band of approximately 65 kDa, both under nonreducing and reducing conditions. These data indicate that ED6 and LD6 mAb recognize a novel non-lineage-specific activation antigen which is involved in the induction of the functional program of long-term cultured T or natural killer cells.

摘要

用表达T细胞受体(TcR)γ/δ的细胞毒性T细胞系免疫小鼠,获得了两种单克隆抗体(mAb),分别命名为ED6和LD6。根据它们在重定向杀伤试验中触发免疫细胞系溶细胞程序的能力,选择了这些mAb。两种mAb都识别大多数长期培养的TcRγ/δ +、TcRα/β +和CD3 - CD16 +淋巴细胞表面表达的分子,而静止外周血淋巴细胞表面没有这种分子。此外,两种mAb都与肿瘤性B细胞系、爱泼斯坦 - 巴尔病毒转化的B细胞系、小细胞肺癌和胶质瘤细胞系发生反应,而在卵巢癌、乳腺癌、结肠癌和非小细胞肺癌细胞系上未检测到表面反应性。通过两种溶细胞试验研究了这些mAb的功能活性。在4小时的51Cr释放试验中,两种mAb都能够触发CD3 + TcRγ/δ +多克隆细胞系和一个CD3 - CD16 + NK细胞克隆针对小鼠肥大细胞瘤靶细胞系P815(Fc受体+)的溶细胞程序。此外,ED6和LD6杂交瘤被TcRγ/δ +效应细胞裂解,而其他杂交瘤(来自同一融合)未被裂解。ED6和LD6 mAb(在亚致有丝分裂剂量的佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯存在下)还诱导表达TcRγ/δ或α/β的ED6/LD6 + T细胞克隆分泌白细胞介素2。mAb诱导的表面抗原调节实验表明,ED6和LD6识别的抗原决定簇共同调节,因此表明这两种mAb可能识别相同或紧密相关的分子。通过蛋白质印迹分析研究了mAb识别的抗原的分子特征。在非还原和还原条件下,LD6 mAb都识别一条约65 kDa的主要条带。这些数据表明,ED6和LD6 mAb识别一种新的非谱系特异性激活抗原,该抗原参与长期培养的T细胞或自然杀伤细胞功能程序的诱导。

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