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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.

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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