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先天免疫细胞调控脂肪组织生物学。

Innate T Cells Govern Adipose Tissue Biology.

机构信息

Division of Rheumatology, Immunology, and Allergy, Harvard Medical School, Boston, MA 02115; and.

Division of Genetics, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115.

出版信息

J Immunol. 2018 Oct 1;201(7):1827-1834. doi: 10.4049/jimmunol.1800556.

DOI:10.4049/jimmunol.1800556
PMID:30224362
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6201318/
Abstract

During the past 25 y, the immune system has appeared as a key regulator of adipose tissue biology and metabolic homeostasis. In lean animals, adipose-resident leukocytes maintain an anti-inflammatory microenvironment that preserves the proper functioning of the tissue. In this review, we describe two populations of innate T cells enriched in adipose tissue, invariant NKT and γδ T cells, and how they serve overlapping and nonredundant roles in controlling adipose tissue functions. These cells interact with and expand anti-inflammatory regulatory T cells and M2 macrophages, thereby driving a metabolically beneficial tissue milieu. Surprisingly, we have found that adipose invariant NKT and γδ T cells also promote weight loss and heat production in a process called "nonshivering thermogenesis." The data surrounding these two cell types highlight their powerful ability to regulate not only other leukocytes, but also tissue-wide processes that affect an entire organism.

摘要

在过去的 25 年中,免疫系统似乎成为了脂肪组织生物学和代谢稳态的关键调节因子。在瘦素动物中,脂肪组织驻留的白细胞维持着抗炎的微环境,从而保持组织的正常功能。在这篇综述中,我们描述了在脂肪组织中富集的两种先天 T 细胞群体,即不变自然杀伤 T(invariant natural killer T,iNKT)细胞和 γδ T 细胞,以及它们如何在控制脂肪组织功能方面发挥重叠但非冗余的作用。这些细胞与抗炎性调节性 T 细胞和 M2 巨噬细胞相互作用并使其扩增,从而促进有益代谢的组织微环境。令人惊讶的是,我们发现脂肪组织中的 iNKT 和 γδ T 细胞也能促进体重减轻和产热,这一过程被称为“非颤抖性产热”。围绕这两种细胞类型的数据突出了它们强大的调节能力,不仅能调节其他白细胞,还能调节影响整个生物体的组织范围的过程。

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本文引用的文献

1
γδ T cells producing interleukin-17A regulate adipose regulatory T cell homeostasis and thermogenesis.γδ T 细胞产生白细胞介素-17A 调节脂肪组织调节性 T 细胞的动态平衡和产热。
Nat Immunol. 2018 May;19(5):464-474. doi: 10.1038/s41590-018-0094-2. Epub 2018 Apr 18.
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FGF19, FGF21, and an FGFR1/β-Klotho-Activating Antibody Act on the Nervous System to Regulate Body Weight and Glycemia.成纤维细胞生长因子 19、21 和一种 FGFR1/β-Klotho 激活抗体通过作用于神经系统来调节体重和血糖。
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Brown-adipose-tissue macrophages control tissue innervation and homeostatic energy expenditure.棕色脂肪组织巨噬细胞控制组织神经支配和稳态能量消耗。
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M2-specific reduction of CD1d switches NKT cell-mediated immune responses and triggers metaflammation in adipose tissue.M2 型特异性降低 CD1d 可转换 NKT 细胞介导的免疫应答,并引发脂肪组织的代谢炎症。
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Mitochondrial Patch Clamp of Beige Adipocytes Reveals UCP1-Positive and UCP1-Negative Cells Both Exhibiting Futile Creatine Cycling.米色脂肪细胞的线粒体膜片钳研究揭示UCP1阳性和UCP1阴性细胞均存在无效的肌酸循环。
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Adipose Type One Innate Lymphoid Cells Regulate Macrophage Homeostasis through Targeted Cytotoxicity.脂肪组织 I 型固有淋巴细胞通过靶向细胞毒性调节巨噬细胞动态平衡。
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iNKT Cells Induce FGF21 for Thermogenesis and Are Required for Maximal Weight Loss in GLP1 Therapy.iNKT细胞诱导成纤维细胞生长因子21进行产热,且在胰高血糖素样肽1治疗中实现最大程度体重减轻时是必需的。
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