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T细胞生命中的核因子-κB信号网络。

The NF-κB signaling network in the life of T cells.

作者信息

Daniels Mark A, Teixeiro Emma

机构信息

Department of Molecular Microbiology and Immunology, School of Medicine, University of Missouri, Columbia, MO, United States.

Roy Blunt NextGen Precision Health Building, University of Missouri, Columbia, MO, United States.

出版信息

Front Immunol. 2025 Apr 30;16:1559494. doi: 10.3389/fimmu.2025.1559494. eCollection 2025.


DOI:10.3389/fimmu.2025.1559494
PMID:40370445
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12075310/
Abstract

NF-κB is a crucial transcription factor in lymphocyte signaling. It is activated by environmental cues that drive lymphocyte differentiation to combat infections and cancer. As a key player in inflammation, NF-κB also significantly impacts autoimmunity and transplant rejection, making it an important therapeutic target. While the signaling molecules regulating this pathway are well-studied, the effect of changes in NF-κB signaling levels on T lymphocyte differentiation, fate, and function is not fully understood. Advances in computational biology and new NF-κB-inducible animal models are beginning to clarify these questions. In this review, we highlight recent findings related to T cells, focusing on how environmental cues affecting NF-κB signaling levels determine T cell fate and function.

摘要

核因子-κB(NF-κB)是淋巴细胞信号传导中的关键转录因子。它被驱动淋巴细胞分化以对抗感染和癌症的环境信号激活。作为炎症中的关键因子,NF-κB也对自身免疫和移植排斥有显著影响,使其成为重要的治疗靶点。虽然调节该信号通路的信号分子已得到充分研究,但NF-κB信号水平变化对T淋巴细胞分化、命运和功能的影响尚未完全明确。计算生物学的进展和新型NF-κB诱导动物模型开始阐明这些问题。在本综述中,我们重点介绍与T细胞相关的最新发现,着重探讨影响NF-κB信号水平的环境信号如何决定T细胞的命运和功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c371/12075310/af530b477b16/fimmu-16-1559494-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c371/12075310/e2cc04a0e329/fimmu-16-1559494-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c371/12075310/0b1ae65a9ef0/fimmu-16-1559494-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c371/12075310/76fa9a39d551/fimmu-16-1559494-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c371/12075310/af530b477b16/fimmu-16-1559494-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c371/12075310/e2cc04a0e329/fimmu-16-1559494-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c371/12075310/0b1ae65a9ef0/fimmu-16-1559494-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c371/12075310/76fa9a39d551/fimmu-16-1559494-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c371/12075310/af530b477b16/fimmu-16-1559494-g004.jpg

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The NF-κB signaling network in the life of T cells.

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引用本文的文献

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Cell Mol Life Sci. 2025-9-2

[2]
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本文引用的文献

[1]
NF-κB subunits RelA and c-Rel selectively control CD4+ T cell function in multiple sclerosis and cancer.

J Exp Med. 2024-6-3

[2]
NF-κB in biology and targeted therapy: new insights and translational implications.

Signal Transduct Target Ther. 2024-3-4

[3]
The transcription factor NF-κB orchestrates nucleosome remodeling during the primary response to Toll-like receptor 4 signaling.

Immunity. 2024-3-12

[4]
Prevention of respiratory virus transmission by resident memory CD8 T cells.

Nature. 2024-2

[5]
Unrestrained cleavage of Roquin-1 by MALT1 induces spontaneous T cell activation and the development of autoimmunity.

Proc Natl Acad Sci U S A. 2023-11-28

[6]
IKK2/NFkB signaling controls lung resident CD8 T cell memory during influenza infection.

Nat Commun. 2023-7-19

[7]
A guide to thymic selection of T cells.

Nat Rev Immunol. 2024-2

[8]
TCR-independent CD137 (4-1BB) signaling promotes CD8-exhausted T cell proliferation and terminal differentiation.

Immunity. 2023-7-11

[9]
Localization, tissue biology and T cell state - implications for cancer immunotherapy.

Nat Rev Immunol. 2023-12

[10]
CD4 T cell memory.

Nat Immunol. 2023-6

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