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CD3阴性淋巴因子激活的细胞毒性细胞表达CD3ε基因。

CD3-negative lymphokine-activated cytotoxic cells express the CD3 epsilon gene.

作者信息

Biassoni R, Ferrini S, Prigione I, Moretta A, Long E O

机构信息

Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892.

出版信息

J Immunol. 1988 Mar 1;140(5):1685-9.

PMID:2894394
Abstract

The expression of genes encoding different polypeptide chains of the TCR-CD3 complex was analyzed in a panel of cloned MHC-unrestricted cytotoxic cells. The clones were derived from CD3+ and CD3- human PBL. After expansion in rIL-2, all clones were able to lyse the NK-sensitive target cell line K562. In contrast, lysis of fresh tumor cells was achieved almost exclusively by CD3- clones. To test whether a known TCR-CD3 complex may be involved in MHC-unrestricted cytotoxicity, total RNA from nine CD3+ and 11 CD3- clones was isolated and hybridized with DNA probes for the TCR alpha-, beta-, and gamma-chains and for the CD3 gamma-, delta-, and epsilon-chains. TCR gamma transcripts were present at high levels in CD3+CD4- CD8- clones but were undetectable in all CD3- clones. Lysis of fresh tumor cells is an activity which can be independent of the TCR alpha beta and TCR gamma complexes because the CD3- clones did not express these TCR genes. Interestingly, all CD3- clones expressed CD3 epsilon transcripts, but not CD3 gamma- or delta-transcripts. CD3- lymphokine-activated cytotoxic cells may therefore be derived from immature T cells which do not yet express a complete CD3 complex. The CD3 epsilon chain, if expressed in CD3- cells in association with other molecules, could be involved in the activation and lytic function of these MHC-unrestricted cytotoxic cells.

摘要

在一组克隆的MHC非限制性细胞毒性细胞中分析了编码TCR-CD3复合物不同多肽链的基因表达。这些克隆来源于CD3 +和CD3 -的人外周血淋巴细胞(PBL)。在rIL-2中扩增后,所有克隆都能够裂解NK敏感靶细胞系K562。相比之下,新鲜肿瘤细胞的裂解几乎完全由CD3 -克隆实现。为了测试已知的TCR-CD3复合物是否可能参与MHC非限制性细胞毒性,从9个CD3 +和11个CD3 -克隆中分离出总RNA,并与针对TCRα、β和γ链以及CD3γ、δ和ε链的DNA探针杂交。TCRγ转录本在CD3 + CD4 - CD8 -克隆中高水平存在,但在所有CD3 -克隆中均未检测到。新鲜肿瘤细胞的裂解是一种可以独立于TCRαβ和TCRγ复合物的活性,因为CD3 -克隆不表达这些TCR基因。有趣的是,所有CD3 -克隆都表达CD3ε转录本,但不表达CD3γ或δ转录本。因此,CD3 -淋巴因子激活的细胞毒性细胞可能来源于尚未表达完整CD3复合物的未成熟T细胞。如果CD3ε链与其他分子一起在CD3 -细胞中表达,则可能参与这些MHC非限制性细胞毒性细胞的激活和裂解功能。

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