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B细胞谱系中的AMPK代谢调节体液免疫反应。

AMPK Metabolism in the B Lineage Modulates Humoral Responses.

作者信息

Brookens Shawna K, Boothby Mark R

机构信息

Cancer Biology Program, Vanderbilt University, Nashville, TN 37232, USA.

Department of Pathology-Microbiology-Immunology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.

出版信息

Immunometabolism. 2021;3(2). doi: 10.20900/immunometab20210011. Epub 2021 Feb 12.

DOI:10.20900/immunometab20210011
PMID:33717606
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7951989/
Abstract

A large and growing body of evidence supports functions of enzymes that regulate or effect cellular metabolism in governing the development, survival, and effector functions of immune cells-especially T cells, macrophages, and dendritic cells. Among these proteins, adenosine monophosphate-activated protein kinase (AMPK) is a conserved ATP and nutrient sensor that regulates multiple metabolic pathways to promote energy homeostasis. Although AMPK had been shown to regulate aspects of CD4 and CD8 T cell biology, its function in B lymphocytes has been less clear. Here, we review recent advances in our understanding of the role of AMPK in the metabolism, function, and maintenance of the B lineage.

摘要

大量且不断增加的证据支持这样的观点

调节或影响细胞代谢的酶在控制免疫细胞(尤其是T细胞、巨噬细胞和树突状细胞)的发育、存活和效应功能方面发挥作用。在这些蛋白质中,腺苷单磷酸激活的蛋白激酶(AMPK)是一种保守的ATP和营养传感器,可调节多种代谢途径以促进能量稳态。尽管已证明AMPK可调节CD4和CD8 T细胞生物学的多个方面,但其在B淋巴细胞中的功能尚不清楚。在此,我们综述了近年来对AMPK在B细胞系的代谢、功能和维持中的作用的理解进展。

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本文引用的文献

1
AMPKα1 in B Cells Dampens Primary Antibody Responses yet Promotes Mitochondrial Homeostasis and Persistence of B Cell Memory.B 细胞中的 AMPKα1 抑制初级抗体应答,但促进 B 细胞记忆的线粒体稳态和持久存在。
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Exit from germinal center to become quiescent memory B cells depends on metabolic reprograming and provision of a survival signal.从中胚层中心退出成为静止记忆 B 细胞依赖于代谢重编程和提供生存信号。
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Infection-induced plasmablasts are a nutrient sink that impairs humoral immunity to malaria.
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Downregulation of LKB1/AMPK Signaling in Blood Mononuclear Cells Is Associated with the Severity of Guillain-Barre Syndrome.血液单核细胞中 LKB1/AMPK 信号的下调与吉兰-巴雷综合征的严重程度相关。
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Redox regulation of the immune response.氧化还原调节免疫反应。
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Protection of Quiescence and Longevity of IgG Memory B Cells by Mitochondrial Autophagy.线粒体自噬保护 IgG 记忆 B 细胞的静止和长寿。
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Altered Germinal-Center Metabolism in B Cells in Autoimmunity.自身免疫中B细胞生发中心代谢的改变。
Metabolites. 2022 Jan 5;12(1):40. doi: 10.3390/metabo12010040.
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Supplying the trip to antibody production-nutrients, signaling, and the programming of cellular metabolism in the mature B lineage.供应抗体产生所需的物质——营养物质、信号以及成熟 B 细胞谱系中细胞代谢的编程。
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Nat Immunol. 2020 Jul;21(7):790-801. doi: 10.1038/s41590-020-0678-5. Epub 2020 May 18.
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Nat Immunol. 2020 Mar;21(3):331-342. doi: 10.1038/s41590-020-0598-4. Epub 2020 Feb 17.
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mTORC1 coordinates an immediate unfolded protein response-related transcriptome in activated B cells preceding antibody secretion.mTORC1 在激活的 B 细胞中协调与未折叠蛋白反应相关的转录组,以促进抗体分泌。
Nat Commun. 2020 Feb 5;11(1):723. doi: 10.1038/s41467-019-14032-1.
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Metabolic requirements of human pro-inflammatory B cells in aging and obesity.人类致炎 B 细胞在衰老和肥胖中的代谢需求。
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Initial B Cell Activation Induces Metabolic Reprogramming and Mitochondrial Remodeling.初始B细胞活化诱导代谢重编程和线粒体重塑。
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