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T细胞受体(TcR)α/β异二聚体的基因重组可恢复CD3ζ2与TcR/CD3复合物的结合。

Genetic reconstitution of the T cell receptor (TcR) alpha/beta heterodimer restores the association of CD3 zeta 2 with the TcR/CD3 complex.

作者信息

Blumberg R S, Sancho J, Ley S C, McDermott F V, Tan K N, Breitmeyer J, Terhorst C

机构信息

Laboratories of Molecular Immunology, Dana-Farber Cancer Institute, Boston MA.

出版信息

Eur J Immunol. 1991 Feb;21(2):473-81. doi: 10.1002/eji.1830210233.

Abstract

The cell surface expression of the T cell receptor (TcR)/CD3 complex and, consequently, the functional competence of the cell is partly dependent on CD3 zeta. In its absence, a pentameric complex (TcR alpha/beta/CD3 gamma delta epsilon) is formed which is inefficiently transported to the cell surface. Reconstitution of CD3 zeta by transfection, in turn, restores the cell surface expression and function of the complex. Through the use of transfection experiments, we here provide direct evidence that the association of CD3 zeta 2 with the TcR/CD3 complex is dependent on the presence of both the TcR alpha and beta polypeptide chains. Despite wild-type levels of the CD3 zeta protein in a TcR alpha-negative mutant human T cell line, a complex was formed intracellularly which lacked CD3 zeta 2 and consisted of beta gamma delta epsilon and beta 2 gamma delta epsilon. Upon transfection of the mutant with a TcR alpha cDNA, a TcR/CD3 complex which contained CD3 zeta 2 was observed intracellularly. In contrast to the partial subcomplex on the cell surface of the untransfected cell line, the TcR/CD3 complex on the transfectant was functional as demonstrated by its ability to mobilize intracellular calcium after stimulation with a mitogenic CD3 epsilon-specific monoclonal antibody. Transient transfection studies performed in COS cell fibroblasts indicated that CD3 zeta 2 was not interacting with the TcR alpha protein alone, implying that a conformation provided by either the TcR alpha/beta heterodimer or the TcR alpha/beta/CD3 gamma delta epsilon complex was necessary for the association of CD3 zeta 2. Transfection studies performed in a TcR alpha/beta-negative murine T-T hybridoma confirmed the requirement of both the TcR alpha and beta proteins in CD3 zeta 2 binding. We conclude that the TcR alpha and beta chains harbor polypeptide sequences essential for the association of CD3 zeta 2 with the TcR/CD3 complex.

摘要

T细胞受体(TcR)/CD3复合物在细胞表面的表达,进而细胞的功能活性部分依赖于CD3ζ。在缺乏CD3ζ的情况下,会形成一种五聚体复合物(TcRα/β/CD3γδε),其向细胞表面的转运效率低下。通过转染重建CD3ζ,反过来又能恢复复合物在细胞表面的表达和功能。通过转染实验,我们在此提供直接证据表明,CD3ζ2与TcR/CD3复合物的结合依赖于TcRα和β多肽链的同时存在。尽管在一个TcRα阴性的突变人T细胞系中CD3ζ蛋白水平为野生型,但在细胞内形成了一种缺乏CD3ζ2的复合物,该复合物由βγδε和β2γδε组成。用TcRα cDNA转染该突变体后,在细胞内观察到一种含有CD3ζ2的TcR/CD3复合物。与未转染细胞系细胞表面的部分亚复合物不同,转染细胞上的TcR/CD3复合物具有功能,这通过其在用促有丝分裂的CD3ε特异性单克隆抗体刺激后动员细胞内钙的能力得以证明。在COS细胞成纤维细胞中进行的瞬时转染研究表明,CD3ζ2并非单独与TcRα蛋白相互作用,这意味着由TcRα/β异二聚体或TcRα/β/CD3γδε复合物提供的构象对于CD3ζ2的结合是必要的。在一个TcRα/β阴性的小鼠T-T杂交瘤中进行的转染研究证实了CD3ζ2结合中TcRα和β蛋白两者的必要性。我们得出结论,TcRα和β链含有对于CD3ζ2与TcR/CD3复合物结合至关重要的多肽序列。

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