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γδT细胞受体CD3复合物中的激活诱导修饰。

Activation-induced modification in the CD3 complex of the gammadelta T cell receptor.

作者信息

Hayes Sandra M, Laky Karen, El-Khoury Dalal, Kappes Dietmar J, Fowlkes B J, Love Paul E

机构信息

Laboratory of Mammalian Genes and Development, National Institute of Child Health and Human Development, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

J Exp Med. 2002 Nov 18;196(10):1355-61. doi: 10.1084/jem.20021196.

Abstract

The T cell antigen receptor complexes expressed on alphabeta and gammadelta T cells differ not only in their respective clonotypic heterodimers but also in the subunit composition of their CD3 complexes. The gammadelta T cell receptors (TCRs) expressed on ex vivo gammadelta T cells lack CD3delta, whereas alphabeta TCRs contain CD3delta. While this result correlates with the phenotype of CD3delta(-/-) mice, in which gammadelta T cell development is unaffected, it is inconsistent with the results of previous studies reporting that CD3delta is a component of the gammadelta TCR. Since earlier studies examined the subunit composition of gammadelta TCRs expressed on activated and expanded peripheral gammadelta T cells or gammadelta TCR(+) intestinal intraepithelial lymphocytes, we hypothesized that activation and expansion may lead to changes in the CD3 subunit composition of the gammadelta TCR. Here, we report that activation and expansion do in fact result in the inclusion of a protein, comparable in mass and mobility to CD3delta, in the gammadelta TCR. Further analyses revealed that this protein is not CD3delta, but instead is a differentially glycosylated form of CD3gamma. These results provide further evidence for a major difference in the subunit composition of alphabeta- and gammadelta TCR complexes and raise the possibility that modification of CD3gamma may have important functional consequences in activated gammadelta T cells.

摘要

在αβ和γδ T细胞上表达的T细胞抗原受体复合物不仅在各自的克隆型异二聚体上存在差异,而且在其CD3复合物的亚基组成上也有所不同。体外γδ T细胞上表达的γδ T细胞受体(TCR)缺乏CD3δ,而αβ TCR含有CD3δ。虽然这一结果与CD3δ基因敲除小鼠的表型相关,在该小鼠中γδ T细胞的发育未受影响,但这与先前研究报道CD3δ是γδ TCR的一个组成部分的结果不一致。由于早期研究检测的是活化和扩增的外周γδ T细胞或γδ TCR阳性肠上皮内淋巴细胞上表达的γδ TCR的亚基组成,我们推测激活和扩增可能会导致γδ TCR的CD3亚基组成发生变化。在此,我们报道激活和扩增实际上确实导致γδ TCR中包含一种蛋白质,其质量和迁移率与CD3δ相当。进一步分析表明,这种蛋白质不是CD3δ,而是CD3γ的一种糖基化形式不同的变体。这些结果为αβ和γδ TCR复合物的亚基组成存在重大差异提供了进一步证据,并增加了CD3γ的修饰可能在活化的γδ T细胞中产生重要功能后果的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbb6/2193986/90f8f450b6ed/20021196f1.jpg

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