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是时候团结起来了:胸腺基质细胞在T细胞选择和器官完整性中的多样性与协调性

It's Time to Unite: Diversity and Coordination of Thymic Stromal Cells for T Cell Selection and Organ Integrity.

作者信息

Muro Ryunosuke, Nitta Takeshi

机构信息

Division of Molecular Pathology, Research Institute for Biomedical Sciences, Tokyo University of Science, Chiba, Japan.

出版信息

Immunol Rev. 2025 Jul;332(1):e70040. doi: 10.1111/imr.70040.

DOI:10.1111/imr.70040
PMID:40464763
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12136023/
Abstract

The thymus is a primary lymphoid organ for generating a diverse yet self-tolerant T cell repertoire. Among the thymic stromal cells that create the thymic microenvironment, thymic epithelial cells (TECs) have received the most attention because of their distinctive functions in the repertoire selection of T cells. Other types of thymic stromal cells, such as fibroblasts and endothelial cells, have been less studied, and thus their thymus-specific nature and functions remain unclear. Recent advances in single-cell technologies, multicolor flow cytometry, and sophisticated mouse models have enabled the identification not only of TECs but also of non-TEC stromal cell diversity and the characterization of these cell subpopulations. This review provides a state-of-the-art overview of the thymic microenvironment, focusing on the development and functional diversity of TECs and non-TEC stromal cells. In particular, the recently discovered role of non-TEC stromal cells in thymic organogenesis, T cell selection, and involution and regeneration of the postnatal thymus is highlighted.

摘要

胸腺是一个主要的淋巴器官,用于产生多样化且自身耐受的T细胞库。在构成胸腺微环境的胸腺基质细胞中,胸腺上皮细胞(TECs)因其在T细胞库选择中的独特功能而受到最多关注。其他类型的胸腺基质细胞,如成纤维细胞和内皮细胞,研究较少,因此它们的胸腺特异性性质和功能仍不清楚。单细胞技术、多色流式细胞术和复杂小鼠模型的最新进展,不仅能够识别TECs,还能识别非TEC基质细胞的多样性,并对这些细胞亚群进行表征。本综述提供了胸腺微环境的最新概述,重点关注TECs和非TEC基质细胞的发育和功能多样性。特别是,强调了非TEC基质细胞在胸腺器官发生、T细胞选择以及出生后胸腺退化和再生中的最新发现作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9766/12136023/5fec457c7f8c/IMR-332-0-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9766/12136023/f1a919168987/IMR-332-0-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9766/12136023/215e59df8a3c/IMR-332-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9766/12136023/cf97c2909588/IMR-332-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9766/12136023/5fec457c7f8c/IMR-332-0-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9766/12136023/f1a919168987/IMR-332-0-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9766/12136023/215e59df8a3c/IMR-332-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9766/12136023/cf97c2909588/IMR-332-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9766/12136023/5fec457c7f8c/IMR-332-0-g004.jpg

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本文引用的文献

1
Endogenous thymic regeneration: restoring T cell production following injury.内源性胸腺再生:损伤后恢复T细胞生成
Nat Rev Immunol. 2025 Jan 6. doi: 10.1038/s41577-024-01119-0.
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Cross-species analyses of thymic mimetic cells reveal evolutionarily ancient origins and both conserved and species-specific elements.胸腺模拟细胞的跨物种分析揭示了其在进化上古老的起源以及保守和物种特异性的元素。
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Direct and indirect RANK and CD40 signaling regulate the maintenance of thymic epithelial cell frequency and properties in the adult thymus.
直接和间接的RANK及CD40信号传导调节成年胸腺中胸腺上皮细胞频率和特性的维持。
Front Immunol. 2024 Nov 29;15:1500908. doi: 10.3389/fimmu.2024.1500908. eCollection 2024.
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Platelet factor 4-induced T1-T polarization suppresses antitumor immunity.血小板因子 4 诱导的 T1-T 极化抑制抗肿瘤免疫。
Science. 2024 Nov 22;386(6724):eadn8608. doi: 10.1126/science.adn8608.
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A spatial human thymus cell atlas mapped to a continuous tissue axis.空间人类胸腺细胞图谱绘制到连续的组织轴上。
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Neural Crest-Derived Mesenchymal Cells Support Thymic Reconstitution After Lethal Irradiation.神经嵴来源的间充质细胞支持致死性照射后的胸腺重建。
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Transcript splicing optimizes the thymic self-antigen repertoire to suppress autoimmunity.转录剪接优化了胸腺自身抗原库,以抑制自身免疫。
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