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一种新型的小鼠骨髓造血干细胞标志物,在外周T细胞上表达,并与活化的细胞毒性T淋巴细胞上的一种功能重要分子相关。

A novel marker of murine bone marrow hematopoietic stem cells that is expressed on peripheral T cells and is associated with a functionally important molecule on activated cytotoxic T lymphocytes.

作者信息

Mosley R L, Hamad M, Whetsell M, Klein J R

机构信息

Department of Biological Science, University of Tulsa, Oklahoma 74104.

出版信息

Hybridoma. 1994 Oct;13(5):353-8. doi: 10.1089/hyb.1994.13.353.

Abstract

A MAb (R2/60) has been isolated that defines a novel lymphocyte marker of murine T cells. The determinant recognized by MAb R2/60 is present on a subset of bone marrow (BM) hematopoietic stem cells, on adult thymocytes, on peripheral T cells (both resting and activated), and on murine T cell tumor lines, although it is not expressed on mature B cells. In immunoprecipitation studies using radiolabeled membrane lysates from adult thymocytes, MAb R2/60 precipitated a 44-kDa membrane-bound dimer. Functionally, MAb R2/60 mediated antigen-independent cell lysis by activated CTLs, and by CTL clones, when bridged to Fc receptor-bearing target cells; however, binding of MAb R2/60 to effector cells prior to cytotoxic assays did not inhibit target cell lysis by CTLs, suggesting that the R2/60 determinant is involved in transmembrane signaling to already activated CTLs, but that it is not involved in target cell adhesion or antigen recognition. Moreover, direct stimulation of T cells by MAb R2/60 in the absence of additional stimuli did not induce cell proliferation, further implying that the R2/60 determinant is functionally involved in the effector rather than the inductive phase of the T cell response.

摘要

已分离出一种单克隆抗体(R2/60),它定义了一种新型的小鼠T细胞淋巴细胞标志物。单克隆抗体R2/60识别的决定簇存在于一部分骨髓(BM)造血干细胞、成年胸腺细胞、外周T细胞(静息和活化的)以及小鼠T细胞肿瘤系上,尽管它在成熟B细胞上不表达。在使用成年胸腺细胞放射性标记膜裂解物的免疫沉淀研究中,单克隆抗体R2/60沉淀出一种44 kDa的膜结合二聚体。在功能上,当单克隆抗体R2/60与带有Fc受体的靶细胞连接时,它介导活化的细胞毒性T淋巴细胞(CTL)和CTL克隆进行非抗原依赖性细胞裂解;然而,在细胞毒性测定之前,单克隆抗体R2/60与效应细胞的结合并不抑制CTL对靶细胞的裂解,这表明R2/60决定簇参与了向已活化CTL的跨膜信号传导,但不参与靶细胞黏附或抗原识别。此外,在没有额外刺激的情况下,单克隆抗体R2/60直接刺激T细胞不会诱导细胞增殖,这进一步表明R2/60决定簇在功能上参与T细胞反应的效应阶段而非诱导阶段。

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