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胸腺微环境:固有免疫细胞与发育中的胸腺细胞的相互作用。

Thymic Microenvironment: Interactions Between Innate Immune Cells and Developing Thymocytes.

机构信息

Department of Immunology, University of Toronto, Toronto, ON, Canada.

Biological Sciences, Sunnybrook Research Institute, Toronto, ON, Canada.

出版信息

Front Immunol. 2022 Apr 8;13:885280. doi: 10.3389/fimmu.2022.885280. eCollection 2022.


DOI:10.3389/fimmu.2022.885280
PMID:35464404
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9024034/
Abstract

The thymus is a crucial organ for the development of T cells. T cell progenitors first migrate from the bone marrow into the thymus. During the journey to become a mature T cell, progenitors require interactions with many different cell types within the thymic microenvironment, such as stromal cells, which include epithelial, mesenchymal and other non-T-lineage immune cells. There are two crucial decision steps that are required for generating mature T cells: positive and negative selection. Each of these two processes needs to be performed efficiently to produce functional MHC-restricted T cells, while simultaneously restricting the production of auto-reactive T cells. In each step, there are various cell types that are required for the process to be carried out suitably, such as scavengers to clean up apoptotic thymocytes that fail positive or negative selection, and antigen presenting cells to display self-antigens during positive and negative selection. In this review, we will focus on thymic non-T-lineage immune cells, particularly dendritic cells and macrophages, and the role they play in positive and negative selection. We will also examine recent advances in the understanding of their participation in thymus homeostasis and T cell development. This review will provide a perspective on how the thymic microenvironment contributes to thymocyte differentiation and T cell maturation.

摘要

胸腺是 T 细胞发育的关键器官。T 细胞前体首先从骨髓迁移到胸腺。在成为成熟 T 细胞的过程中,前体需要与胸腺微环境中的许多不同类型的细胞相互作用,如基质细胞,包括上皮细胞、间充质细胞和其他非 T 细胞谱系免疫细胞。产生成熟 T 细胞需要经历两个关键的决策步骤:阳性选择和阴性选择。这两个过程都需要高效地进行,以产生功能性 MHC 限制的 T 细胞,同时限制自身反应性 T 细胞的产生。在每个步骤中,都需要各种类型的细胞来完成这个过程,例如清除在阳性或阴性选择中失败的凋亡胸腺细胞的清道夫,以及在阳性和阴性选择中展示自身抗原的抗原呈递细胞。在这篇综述中,我们将重点讨论胸腺中非 T 细胞谱系免疫细胞,特别是树突状细胞和巨噬细胞,以及它们在阳性选择和阴性选择中所起的作用。我们还将研究近年来对它们参与胸腺稳态和 T 细胞发育的理解的最新进展。这篇综述将提供一个视角,了解胸腺微环境如何促进胸腺细胞分化和 T 细胞成熟。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d11b/9024034/a62ccc978b4c/fimmu-13-885280-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d11b/9024034/d62e73399724/fimmu-13-885280-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d11b/9024034/a62ccc978b4c/fimmu-13-885280-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d11b/9024034/d62e73399724/fimmu-13-885280-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d11b/9024034/a62ccc978b4c/fimmu-13-885280-g002.jpg

相似文献

[1]
Thymic Microenvironment: Interactions Between Innate Immune Cells and Developing Thymocytes.

Front Immunol. 2022

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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Immunol Res. 2012-12

[9]
Antigen-presenting cells and T-lymphocytes homing to the thymus shape T cell development.

Immunol Lett. 2018-10-9

[10]
Indirect presentation in the thymus limits naive and regulatory T-cell differentiation by promoting deletion of self-reactive thymocytes.

Immunology. 2018-2-27

引用本文的文献

[1]
Mutual Interactions Between Microbiota and the Human Immune System During the First 1000 Days of Life.

Biology (Basel). 2025-3-16

[2]
Morphological alterations of the thymus gland in individuals with schizophrenia.

Mol Psychiatry. 2025-3-4

[3]
Morphological characteristics of microenvironment in the human thymus during fetal development.

BMC Res Notes. 2025-3-3

[4]
The thymus road to a T cell: migration, selection, and atrophy.

Front Immunol. 2024

[5]
Evaluating approaches for studying the roles of thymic DCs in T cell development in mice.

Front Immunol. 2024

[6]
TL1A and IL-18 synergy promotes GM-CSF-dependent thymic granulopoiesis in mice.

Cell Mol Immunol. 2024-8

[7]
The Proteostasis of Thymic Stromal Cells in Health and Diseases.

Protein J. 2024-6

[8]
Bidirectional crosstalk between the peripheral nervous system and lymphoid tissues/organs.

Front Immunol. 2023

[9]
Nrf2: A Main Responsive Element of the Toxicity Effect Caused by Trichothecene (T-2) Mycotoxin.

Toxics. 2023-4-21

[10]
Reading the Ts and DCs of thymopoiesis.

Nat Immunol. 2023-3

本文引用的文献

[1]
Thymic macrophages consist of two populations with distinct localization and origin.

Elife. 2022-11-30

[2]
A model of preferential pairing between epithelial and dendritic cells in thymic antigen transfer.

Elife. 2022-1-31

[3]
Specialized transendothelial dendritic cells mediate thymic T-cell selection against blood-borne macromolecules.

Nat Commun. 2021-10-28

[4]
Circulating mature dendritic cells homing to the thymus promote thymic epithelial cells involution via the Jagged1/Notch3 axis.

Cell Death Discov. 2021-8-30

[5]
Infection-Associated Thymic Atrophy.

Front Immunol. 2021

[6]
VSIG4(+) peritoneal macrophages induce apoptosis of double-positive thymocyte via the secretion of TNF-α in a CLP-induced sepsis model resulting in thymic atrophy.

Cell Death Dis. 2021-5-22

[7]
Radiation inducible MafB gene is required for thymic regeneration.

Sci Rep. 2021-5-17

[8]
Thymic development of gut-microbiota-specific T cells.

Nature. 2021-6

[9]
Non-Epithelial Thymic Stromal Cells: Unsung Heroes in Thymus Organogenesis and T Cell Development.

Front Immunol. 2020

[10]
A 2020 View of Thymus Stromal Cells in T Cell Development.

J Immunol. 2021-1-15

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