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胎儿发育过程中人类γδ T细胞库的产生。

The generation of human gammadelta T cell repertoires during fetal development.

作者信息

McVay L D, Jaswal S S, Kennedy C, Hayday A, Carding S R

机构信息

Department of Microbiology, University of Pennsylvania School of Medicine, Philadelphia 19104, USA.

出版信息

J Immunol. 1998 Jun 15;160(12):5851-60.

PMID:9637496
Abstract

The nature of how human gammadelta T cells are normally generated is not clear. We have used an RT-PCR assay and DNA sequencing to identify and compare delta-encoded TCRs (TCRDs) that are generated de novo in the fetal gut, liver, and thymus and to determine when, where, and how the TCRD repertoire is established during normal embryonic development. Rearranged TCRDV genes are first expressed outside of the thymus in the liver and primitive gut between 6 and 9 wk gestation. Although DV1Rs and/or DV2Rs predominated, differences in the pattern of TCRDV gene rearrangement and transcription in each tissue during ontogeny were identified. Specific, DV2-encoded TCRs are highly conserved throughout ontogeny in the tissues from the same and between genetically distinct donors. Although the thymic and intestinal gammadelta T cell repertoires partially overlap early in development, they diverge and become nonoverlapping during the second trimester, and the generation of the intestinal gammadelta T cell repertoire is characterized by differences in the processing of DV1Rs and DV2Rs. Whereas the structural diversity of DV1Rs progressively increases during gut development up to birth, DV2Rs have limited structural diversity throughout ontogeny. Together, our findings provide evidence for the ability of different fetal tissues to support the development of gammadelta T cells.

摘要

人类γδT细胞正常生成的本质尚不清楚。我们使用逆转录聚合酶链反应(RT-PCR)分析和DNA测序来鉴定和比较在胎儿肠道、肝脏和胸腺中从头生成的δ编码T细胞受体(TCRD),并确定在正常胚胎发育过程中TCRD库何时、何地以及如何建立。重排的TCRDV基因首先在妊娠6至9周时在肝脏和原始肠道的胸腺外表达。尽管DV1R和/或DV2R占主导,但在个体发育过程中每个组织中TCRDV基因重排和转录模式的差异得以确定。特定的、DV2编码的TCR在来自相同和遗传上不同供体的组织的整个个体发育过程中高度保守。尽管胸腺和肠道γδT细胞库在发育早期部分重叠,但在妊娠中期它们会分化并变得不重叠,并且肠道γδT细胞库的生成以DV1R和DV2R处理的差异为特征。在肠道发育直至出生的过程中,DV1R的结构多样性逐渐增加,而DV2R在整个个体发育过程中结构多样性有限。总之,我们的研究结果为不同胎儿组织支持γδT细胞发育的能力提供了证据。

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