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T细胞受体δ基因敲除小鼠:αβ T细胞的独立生成及γδ TCR基因的程序性重排

T cell receptor delta gene mutant mice: independent generation of alpha beta T cells and programmed rearrangements of gamma delta TCR genes.

作者信息

Itohara S, Mombaerts P, Lafaille J, Iacomini J, Nelson A, Clarke A R, Hooper M L, Farr A, Tonegawa S

机构信息

Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge 02139.

出版信息

Cell. 1993 Feb 12;72(3):337-48. doi: 10.1016/0092-8674(93)90112-4.

Abstract

T cells bearing T cell receptor (TCR) gamma and delta chain heterodimers are first generated early in ontogeny. They form distinct subsets that differ in their TCR repertoires and tissue distribution. Disruption of the mouse TCR C delta gene segment by a gene targeting method caused the complete loss of T cells bearing TCR gamma delta chains, but had little or no effect on the development of T cells bearing TCR alpha beta chains. The analyses of TCR gamma and delta genes in the mutant mice suggest that intracellular mechanisms acting at the level of DNA rearrangement play key roles in the differential gamma and delta gene rearrangements and in the generation of the highly restricted junctional sequences during fetal thymic development.

摘要

携带T细胞受体(TCR)γ和δ链异二聚体的T细胞在个体发育早期首次产生。它们形成不同的亚群,其TCR库和组织分布有所不同。通过基因靶向方法破坏小鼠TCR Cδ基因片段会导致携带TCRγδ链的T细胞完全丧失,但对携带TCRαβ链的T细胞发育几乎没有影响。对突变小鼠中TCRγ和δ基因的分析表明,在DNA重排水平起作用的细胞内机制在胎儿胸腺发育过程中的γ和δ基因差异重排以及高度受限的连接序列的产生中起关键作用。

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