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通过RORγt+细胞的命运图谱揭示肠道αβ T细胞的胸腺起源

Thymic origin of intestinal alphabeta T cells revealed by fate mapping of RORgammat+ cells.

作者信息

Eberl Gérard, Littman Dan R

机构信息

Molecular Pathogenesis Program, Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY 10016, USA.

出版信息

Science. 2004 Jul 9;305(5681):248-51. doi: 10.1126/science.1096472.

Abstract

Intestinal intraepithelial T lymphocytes (IELs) are likely to play a key role in host mucosal immunity and, unlike other T cells, have been proposed to differentiate from local precursors rather than from thymocytes. We show here that IELs expressing the alphabeta T cell receptor are derived from precursors that express RORgammat, an orphan nuclear hormone receptor detected only in immature CD4+CD8+ thymocytes, fetal lymphoid tissue-inducer (LTi) cells, and LTi-like cells in cryptopatches within the adult intestinal lamina propria. Using cell fate mapping, we found that all intestinal alphabeta T cells are progeny of CD4+CD8+ thymocytes, indicating that the adult intestine is not a significant site for alphabeta T cell development. Our results suggest that intestinal RORgammat+ cells are local organizers of mucosal lymphoid tissue.

摘要

肠道上皮内T淋巴细胞(IELs)可能在宿主黏膜免疫中发挥关键作用,并且与其他T细胞不同,有人提出它们是从局部前体细胞而非胸腺细胞分化而来。我们在此表明,表达αβ T细胞受体的IELs来源于表达RORγt的前体细胞,RORγt是一种仅在未成熟的CD4+CD8+胸腺细胞、胎儿淋巴组织诱导细胞(LTi)以及成年肠道固有层隐窝斑中的LTi样细胞中检测到的孤儿核激素受体。通过细胞命运图谱分析,我们发现所有肠道αβ T细胞都是CD4+CD8+胸腺细胞的后代,这表明成年肠道并非αβ T细胞发育的重要场所。我们的结果表明,肠道RORγt+细胞是黏膜淋巴组织的局部组织者。

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