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成年胸腺γδ细胞中T细胞受体α基因重排与转录

T cell receptor alpha gene rearrangement and transcription in adult thymic gamma delta cells.

作者信息

Mertsching E, Wilson A, MacDonald H R, Ceredig R

机构信息

Unité 184 INSERM, LGME du CNRS, Faculté de Médecine, Strasbourg, France.

出版信息

Eur J Immunol. 1997 Feb;27(2):389-96. doi: 10.1002/eji.1830270208.

Abstract

T cells belong to two separate lineages based on surface expression of alpha beta or gamma delta T cell receptors (TCR). Since during thymus development TCR beta, gamma, and delta genes rearrange before alpha genes, and gamma delta cells appear earlier than alpha beta cells, it has been assumed that gamma delta cells are devoid of TCR alpha rearrangements. We show here that this is not the case, since mature adult, but not fetal, thymic gamma delta cells undergo VJ alpha rearrangements more frequently than immature alpha beta lineage thymic precursors. Sequence analysis shows VJ alpha rearrangements in gamma delta cells to be mostly (70%) nonproductive. Furthermore, VJ alpha rearrangements in gamma delta cells are transcribed normally and, as shown by analysis of TCR beta-/- mice, occur independently of productive VDJ beta rearrangements. These data are interpreted in the context of a model in which precursors of alpha beta and gamma delta cells differ in their ability to express a functional pre-TCR complex.

摘要

根据αβ或γδ T细胞受体(TCR)的表面表达,T细胞属于两个不同的谱系。由于在胸腺发育过程中,TCR β、γ和δ基因在α基因之前重排,并且γδ细胞比αβ细胞出现得更早,因此人们认为γδ细胞没有TCR α重排。我们在此表明情况并非如此,因为成熟的成年胸腺γδ细胞,而非胎儿胸腺γδ细胞,比未成熟的αβ谱系胸腺前体更频繁地发生VJ α重排。序列分析表明,γδ细胞中的VJ α重排大多(70%)是非 productive 的。此外,γδ细胞中的VJ α重排正常转录,并且如对TCR β -/- 小鼠的分析所示,其发生独立于 productive 的VDJ β重排。这些数据在一个模型的背景下进行解释,在该模型中,αβ和γδ细胞的前体在表达功能性前TCR复合物的能力上有所不同。

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