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肾脏免疫稳态中的T细胞代谢

T cell metabolism in kidney immune homeostasis.

作者信息

Liu Zikang, Dai Binbin, Bao Jiwen, Pan Yangbin

机构信息

Department of Nephrology, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.

Center for Medical Research and Innovation, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.

出版信息

Front Immunol. 2024 Dec 16;15:1498808. doi: 10.3389/fimmu.2024.1498808. eCollection 2024.

DOI:10.3389/fimmu.2024.1498808
PMID:39737193
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11684269/
Abstract

Kidney immune homeostasis is intricately linked to T cells. Inappropriate differentiation, activation, and effector functions of T cells lead to a spectrum of kidney disease. While executing immune functions, T cells undergo a series of metabolic rewiring to meet the rapid energy demand. The key enzymes and metabolites involved in T cell metabolism metabolically and epigenetically modulate T cells' differentiation, activation, and effector functions, thereby being capable of modulating kidney immune homeostasis. In this review, we first summarize the latest advancements in T cell immunometabolism. Second, we outline the alterations in the renal microenvironment under certain kidney disease conditions. Ultimately, we highlight the metabolic modulation of T cells within kidney immune homeostasis, which may shed light on new strategies for treating kidney disease.

摘要

肾脏免疫稳态与T细胞有着复杂的联系。T细胞不适当的分化、激活和效应功能会导致一系列肾脏疾病。在执行免疫功能时,T细胞会经历一系列代谢重编程以满足快速的能量需求。参与T细胞代谢的关键酶和代谢产物在代谢和表观遗传水平上调节T细胞的分化、激活和效应功能,从而能够调节肾脏免疫稳态。在这篇综述中,我们首先总结T细胞免疫代谢的最新进展。其次,我们概述某些肾脏疾病条件下肾脏微环境的改变。最后,我们强调肾脏免疫稳态中T细胞的代谢调节,这可能为肾脏疾病的治疗提供新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df5/11684269/dfaffcd944ef/fimmu-15-1498808-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df5/11684269/3b013860e9b2/fimmu-15-1498808-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df5/11684269/dfaffcd944ef/fimmu-15-1498808-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df5/11684269/3b013860e9b2/fimmu-15-1498808-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df5/11684269/dfaffcd944ef/fimmu-15-1498808-g002.jpg

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1
T cell metabolism in kidney immune homeostasis.肾脏免疫稳态中的T细胞代谢
Front Immunol. 2024 Dec 16;15:1498808. doi: 10.3389/fimmu.2024.1498808. eCollection 2024.
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Spatial transcriptomics defines injury specific microenvironments and cellular interactions in kidney regeneration and disease.空间转录组学定义了肾脏再生和疾病中损伤特异性的微环境和细胞相互作用。
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Single-cell multi-omic and spatial profiling of human kidneys implicates the fibrotic microenvironment in kidney disease progression.单细胞多组学和空间分析揭示了人类肾脏纤维化微环境在肾脏疾病进展中的作用。
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Acetyl-CoA carboxylase obstructs CD8 T cell lipid utilization in the tumor microenvironment.
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Modulation of PKM2 inhibits follicular helper T cell differentiation and ameliorates inflammation in lupus-prone mice.PKM2 的调节抑制滤泡辅助性 T 细胞分化并改善狼疮易感小鼠的炎症。
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Nutrients: Signal 4 in T cell immunity.营养素:T 细胞免疫中的信号 4。
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ATP citrate lyase (ACLY)-dependent immunometabolism in mucosal T cells drives experimental colitis in vivo.黏膜T细胞中依赖ATP柠檬酸裂解酶(ACLY)的免疫代谢在体内引发实验性结肠炎。
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Dapagliflozin protects against chronic heart failure in mice by inhibiting macrophage-mediated inflammation, independent of SGLT2.达格列净通过抑制巨噬细胞介导体液炎症来预防小鼠慢性心力衰竭,与 SGLT2 无关。
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