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胆碱代谢的细胞与机体功能

Cellular and organismal function of choline metabolism.

作者信息

Kenny Timothy C, Scharenberg Samantha, Abu-Remaileh Monther, Birsoy Kıvanç

机构信息

Laboratory of Metabolic Regulation and Genetics, The Rockefeller University, New York, NY, USA.

Department of Chemical Engineering, Stanford University, Stanford, CA, USA.

出版信息

Nat Metab. 2025 Jan;7(1):35-52. doi: 10.1038/s42255-024-01203-8. Epub 2025 Jan 8.

Abstract

Choline is an essential micronutrient critical for cellular and organismal homeostasis. As a core component of phospholipids and sphingolipids, it is indispensable for membrane architecture and function. Additionally, choline is a precursor for acetylcholine, a key neurotransmitter, and betaine, a methyl donor important for epigenetic regulation. Consistent with its pleiotropic role in cellular physiology, choline metabolism contributes to numerous developmental and physiological processes in the brain, liver, kidney, lung and immune system, and both choline deficiency and excess are implicated in human disease. Mutations in the genes encoding choline metabolism proteins lead to inborn errors of metabolism, which manifest in diverse clinical pathologies. While the identities of many enzymes involved in choline metabolism were identified decades ago, only recently has the field begun to understand the diverse mechanisms by which choline availability is regulated and fuelled via metabolite transport/recycling and nutrient acquisition. This review provides a comprehensive overview of choline metabolism, emphasizing emerging concepts and their implications for human health and disease.

摘要

胆碱是一种对细胞和机体稳态至关重要的必需微量营养素。作为磷脂和鞘脂的核心成分,它对于膜的结构和功能不可或缺。此外,胆碱是关键神经递质乙酰胆碱以及对表观遗传调控很重要的甲基供体甜菜碱的前体。与其在细胞生理学中的多效性作用一致,胆碱代谢有助于大脑、肝脏、肾脏、肺和免疫系统中的众多发育和生理过程,胆碱缺乏和过量都与人类疾病有关。编码胆碱代谢蛋白的基因突变会导致先天性代谢缺陷,表现为多种临床病理症状。虽然几十年前就已确定了许多参与胆碱代谢的酶的身份,但直到最近该领域才开始了解通过代谢物运输/循环利用和营养获取来调节和供应胆碱可用性的多种机制。本综述全面概述了胆碱代谢,强调了新出现的概念及其对人类健康和疾病的影响。

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Cellular and organismal function of choline metabolism.胆碱代谢的细胞与机体功能
Nat Metab. 2025 Jan;7(1):35-52. doi: 10.1038/s42255-024-01203-8. Epub 2025 Jan 8.
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