脂肪组织Tregs的细胞因子和代谢调节。

Immunometabolism (Cobham (Surrey, England)) Pub Date : 2022-11-01 eCollection Date: 2022-10-01 DOI:10.1097/IN9.0000000000000013
Cody Elkins, Chaoran Li
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引用次数: 1

摘要

自从十多年前它们被发现以来,关于内脏脂肪组织(VAT)常驻调节性T细胞(Tregs)的重要性和功能已经有了很多了解。VAT Tregs在控制VAT炎症和减轻代谢性疾病中起着关键作用。然而,这一人群在肥胖中受到破坏,这加剧了VAT炎症和代谢异常。因此,了解控制稳态和疾病条件下VAT Tregs积累和维持的因素,对于确定肥胖相关代谢疾病的潜在机制和开发新的治疗方法至关重要。VAT Treg区室的扩张和维持受到局部组织微环境因素的强烈影响,包括细胞因子、t细胞受体配体、激素和各种代谢物。这篇综述将主要集中在我们对小鼠附睾VAT (eVAT) Treg的组织微环境因素和细胞代谢过程调控的最新进展,eVAT是最彻底表征VAT Treg群体。我们还将简要讨论关于小鼠卵巢VAT (oVAT) Tregs和人类网膜VAT Tregs调节的有限知识,突出一些遗留问题,并提供该领域发展方向的前瞻性观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Cytokine and metabolic regulation of adipose tissue Tregs.

Since their discovery over a decade ago, much has been learned regarding the importance and function of visceral adipose tissue (VAT)-resident regulatory T cells (Tregs). VAT Tregs play a critical role in controlling VAT inflammation and alleviating metabolic disease. However, this population is disrupted in obesity which exacerbates VAT inflammation and metabolic abnormalities. Therefore, understanding the factors governing the accumulation and maintenance of VAT Tregs, both at steady state and under disease conditions, is crucial for identifying the mechanisms underlying obesity-associated metabolic disease and developing novel therapies. Expansion and maintenance of the VAT Treg compartment is strongly influenced by factors in the local tissue microenvironment, including cytokines, T-cell receptor ligands, hormones, and various metabolites. This mini-review will primarily focus on recent advances in our understandings regarding the regulation of mouse epididymal VAT (eVAT) Tregs, which are the most thoroughly characterized VAT Treg population, by tissue microenvironmental factors and cellular metabolic processes. We will also briefly discuss the limited knowledge available regarding the regulation of mouse ovarian VAT (oVAT) Tregs and human omental VAT Tregs, highlight some lingering questions, and provide a prospective view on where the field is heading.

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