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胸腺球体培养:一种研究人类多克隆非常规T细胞的模型。

ThymoSpheres culture: A model to study human polyclonal unconventional T cells.

作者信息

Billiet Lore, Jansen Hanne, Pille Melissa, Boehme Lena, Sanchez Sanchez Guillem, De Cock Laurenz, Goetgeluk Glenn, Pascal Eva, De Munter Stijn, Deseins Lucas, Ingels Joline, Michiels Thomas, De Vos Robrecht, Zolfaghari Amin, Vandamme Niels, Roels Jana, Kerre Tessa, Dmitriev Ruslan I, Taghon Tom, Vermijlen David, Vandekerckhove Bart

机构信息

Department of Diagnostic Sciences, Ghent University, Ghent, Belgium.

Department of Pharmacotherapy and Pharmaceutics, Université Libre de Bruxelles (ULB), Brussels, Belgium.

出版信息

Eur J Immunol. 2024 Dec;54(12):e2451265. doi: 10.1002/eji.202451265. Epub 2024 Sep 9.

Abstract

In vitro cultures remain crucial for studying the fundamental mechanisms of human T-cell development. Here, we introduce a novel in vitro cultivation system based on ThymoSpheres (TS): dense spheroids consisting of DLL4-expressing stromal cells and human hematopoietic precursor cells, in the absence of thymic epithelial cells. These spheroids are subsequently cultured at the air-liquid interphase. TS generate large numbers of mature T cells, are easy to manipulate, scalable, and can be repeatably sampled to monitor T-cell differentiation. The mature T cells generated from primary human hematopoietic precursor cells were extensively characterized using single-cell RNA and combined T-cell receptor (TCR) sequencing. These predominantly CD8α T cells exhibit transcriptional and TCR CDR3 characteristics similar to the recently described human polyclonal αβ unconventional T cell (UTC) lineage. This includes the expression of hallmark genes associated with agonist selection, such as IKZF2 (Helios), and the expression of various natural killer receptors. The TCR repertoire of these UTCs is polyclonal and enriched for CDR3-associated autoreactive features and early rearrangements of the TCR-α chain. In conclusion, TS cultures offer an intriguing platform to study the development of this human polyclonal UTC lineage and its inducing selection mechanisms.

摘要

体外培养对于研究人类T细胞发育的基本机制仍然至关重要。在此,我们引入了一种基于胸腺球(TS)的新型体外培养系统:在没有胸腺上皮细胞的情况下,由表达DLL4的基质细胞和人类造血前体细胞组成的致密球体。这些球体随后在气液界面进行培养。TS可产生大量成熟T细胞,易于操作、可扩展,并且可以重复取样以监测T细胞分化。使用单细胞RNA和联合T细胞受体(TCR)测序对源自原代人类造血前体细胞的成熟T细胞进行了广泛表征。这些主要为CD8α的T细胞表现出与最近描述的人类多克隆αβ非传统T细胞(UTC)谱系相似的转录和TCR CDR3特征。这包括与激动剂选择相关的标志性基因的表达,如IKZF2(Helios),以及各种自然杀伤受体的表达。这些UTC的TCR库是多克隆的,富含与CDR3相关的自身反应性特征和TCR-α链的早期重排。总之,TS培养为研究这种人类多克隆UTC谱系的发育及其诱导选择机制提供了一个有趣的平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf7/11628907/c8181c896b23/EJI-54-2451265-g003.jpg

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