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一种表位在人游离κ轻链与活化T细胞胞质成分上的共表达。

Co-expression of an epitope on human free kappa-light chains and on a cytoplasmic component in activated T cells.

作者信息

Walker K Z, Hayden G E, Goodnow C C, Boux H A, Adams E, Basten A, Raison R L

出版信息

J Immunol. 1985 Feb;134(2):1059-64.

PMID:2578149
Abstract

K-1-21 is a murine monoclonal antibody that reacts with human kappa-light chains in free form but not when they are associated with immunoglobulin heavy chains. K-1-21 was unexpectedly shown to bind to a determinant, STA (Sezary T cell antigen), detected by immunofluorescence in the cytoplasm but not on the surface of Sezary T cells isolated from peripheral blood (4/4 cases) and in Sezary T cells from lymph node and bone marrow (one patient). STA was detected in F2/F7, CCRF-CEM, Molt-4, and CCRF-HSB (four human T ALL cell lines), in JURKAT (a human T cell leukemia line), and in MLA144 (a Gibbon T cell lymphoma line). It also occurred in Leu-3a+ antigen-specific T cell clones (6/6 tested). Moreover, although STA was absent from freshly isolated normal T cells, its expression could be evoked in E+ cells from peripheral blood by in vitro culture with phytohemagglutinin. Thus, STA appears to be a cytoplasmic marker for activated T cells. Cytoplasmic inhibition immunofluorescence studies indicated that K-1-21 binding to STA in Sezary cells or T cell lines was inhibited by preincubation of the K-1-21 antibody with purified kappa-Bence Jones protein. STA from radiolabeled MLA144 cell lysates was immunoprecipitated by K-1-21 and was identified on polyacrylamide gel electrophoresis under reducing conditions as a protein of m.w. 57,000. Additional experiments are underway to define the molecular basis of the interesting cross-reactivity between a determinant in T cells and the K-1-21 reactive epitope on free kappa-light chains.

摘要

K-1-21是一种鼠单克隆抗体,它能与游离形式的人κ轻链发生反应,但当κ轻链与免疫球蛋白重链结合时则不发生反应。出人意料的是,K-1-21被证明能与一种名为STA(Sezary T细胞抗原)的决定簇结合,该决定簇通过免疫荧光在从外周血分离的Sezary T细胞(4/4例)以及来自淋巴结和骨髓的Sezary T细胞(1例患者)的细胞质中而非表面被检测到。在F2/F7、CCRF-CEM、Molt-4和CCRF-HSB(四个人T-ALL细胞系)、JURKAT(一种人T细胞白血病系)以及MLA144(一种长臂猿T细胞淋巴瘤系)中检测到了STA。它也出现在Leu-3a+抗原特异性T细胞克隆中(6/6检测)。此外,尽管新鲜分离的正常T细胞中不存在STA,但其表达可通过用植物血凝素进行体外培养在外周血的E+细胞中被诱导。因此,STA似乎是活化T细胞的一种细胞质标志物。细胞质抑制免疫荧光研究表明,K-1-21与Sezary细胞或T细胞系中STA的结合可通过将K-1-21抗体与纯化的κ-本斯·琼斯蛋白预孵育而被抑制。来自放射性标记的MLA144细胞裂解物的STA被K-1-21免疫沉淀,并在还原条件下的聚丙烯酰胺凝胶电泳上被鉴定为一种分子量为57,000的蛋白质。正在进行额外的实验以确定T细胞中的一种决定簇与游离κ轻链上K-1-21反应性表位之间有趣的交叉反应性的分子基础。

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