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肠道CD8αα和CD8αβ上皮内淋巴细胞来源于胸腺,并且在TCRβ库中表现出细微差异。

Intestinal CD8 alpha alpha and CD8 alpha beta intraepithelial lymphocytes are thymus derived and exhibit subtle differences in TCR beta repertoires.

作者信息

Imhof B A, Dunon D, Courtois D, Luhtala M, Vainio O

机构信息

Department of Pathology, Geneva University, Geneva, Switzerland.

出版信息

J Immunol. 2000 Dec 15;165(12):6716-22. doi: 10.4049/jimmunol.165.12.6716.

Abstract

Intraepithelial lymphocytes (IEL) of the small intestine are anatomically positioned to be in the first line of cellular defense against enteric pathogens. Therefore, determining the origin of these cells has important implications for the mechanisms of T cell maturation and repertoire selection. Recent evidence suggests that murine CD8 alpha alpha intestinal IELs (iIELs) can mature and undergo selection in the absence of a thymus. We analyzed IEL origin by cell transfer, using two congenic chicken strains. Embryonic day 14 and adult thymocytes did not contain any detectable CD8 alpha alpha T cells. However, when TCR(+) thymocytes were injected into congenic animals, they migrated to the gut and developed into CD8alphaalpha iIELs, while TCR(-) T cell progenitors did not. The TCR V beta 1 repertoire of CD8 alpha alpha(+) TCR V beta 1(+) iIELs contained only part of the TCR V beta 1 repertoire of total iIELs, and it exhibited no new members compared with CD8(+) T cells in the thymus. This indicated that these T cells emigrated from the thymus at an early stage in their developmental process. In conclusion, we show that while CD8 alpha alpha iIELs originate in the thymus, T cells acquire the expression of CD8 alpha alpha homodimers in the gut microenvironment.

摘要

小肠上皮内淋巴细胞(IEL)在解剖学上处于抵御肠道病原体的细胞防御第一线。因此,确定这些细胞的起源对于T细胞成熟和库选择机制具有重要意义。最近的证据表明,小鼠CD8αα肠道IEL(iIEL)可以在没有胸腺的情况下成熟并进行选择。我们使用两种同源鸡品系,通过细胞转移分析IEL的起源。胚胎第14天的胸腺细胞和成年胸腺细胞中未检测到任何CD8ααT细胞。然而,当将TCR(+)胸腺细胞注入同源动物体内时,它们迁移到肠道并发育成CD8αα iIEL,而TCR(-) T细胞祖细胞则不能。CD8αα(+) TCR Vβ1(+) iIEL的TCR Vβ1库仅包含总iIEL的TCR Vβ1库的一部分,与胸腺中的CD8(+) T细胞相比,它没有新的成员。这表明这些T细胞在其发育过程的早期从胸腺迁出。总之,我们表明虽然CD8αα iIEL起源于胸腺,但T细胞在肠道微环境中获得CD8αα同型二聚体的表达。

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