Carrel S, Mach J P, Miescher G, Salvi S, Giuffrè L, Schreyer M, Isler P
Eur J Immunol. 1987 Aug;17(8):1079-87. doi: 10.1002/eji.1830170802.
The T3 complex is known to be expressed on the cell surface of mature T cells together with either the alpha-beta heterodimeric T cell receptor (TCR) or the TCR gamma protein. In a number of immature T cell malignancies, however, T3 has been described exclusively in the cytoplasm. We have investigated five such T cell lines with cytoplasmic T3 and could demonstrate by biosynthetic labeling the presence of the alpha and beta chains of the TCR in the cytoplasm of two of them, CEM and Ichikawa. No surface TCR alpha-beta protein could be detected by staining with the WT31 antibody. These observations, therefore, argue against the concept that expression of the TCR alpha chain controls the surface expression of the T3/TCR complex. Interestingly, phorbol 12-myristate 13-acetate (PMA) induced cell surface expression of T3 protein in these two cell lines only. Moreover, on surface-iodinated CEM cells no association of T3 and TCR molecules could be demonstrated after treatment with PMA, and expression of TCR alpha and beta chains was limited to the cytoplasm. In Ichikawa cells, however, PMA induced surface expression of a mature T3/TCR complex. Our findings indicate that separate regulatory mechanisms may exist for the surface expression of the T3 proteins and for the assembly of the T3/TCR complex.
已知T3复合物与α-β异二聚体T细胞受体(TCR)或TCRγ蛋白一起在成熟T细胞的细胞表面表达。然而,在一些不成熟T细胞恶性肿瘤中,T3仅在细胞质中被描述。我们研究了五个具有细胞质T3的此类T细胞系,并通过生物合成标记证明其中两个细胞系CEM和市川的细胞质中存在TCR的α链和β链。用WT31抗体染色未检测到表面TCRα-β蛋白。因此,这些观察结果与TCRα链的表达控制T3/TCR复合物表面表达的概念相悖。有趣的是,佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)仅在这两个细胞系中诱导T3蛋白的细胞表面表达。此外,在用PMA处理后,在表面碘化的CEM细胞上未证明T3和TCR分子的关联,并且TCRα链和β链的表达仅限于细胞质。然而,在市川细胞中,PMA诱导成熟T3/TCR复合物的表面表达。我们的研究结果表明,T3蛋白的表面表达和T3/TCR复合物的组装可能存在不同的调节机制。