胆碱
线粒体
运输机
膜转运
细胞内
细胞器
膜转运蛋白
细胞生物学
乙酰胆碱
生物化学
化学
膜
生物
内分泌学
基因
作者
Suraj Patil,Oleg Borisov,Nora Scherer,Christophe Wirth,Pascal Schlosser,Matthias Wuttke,Sandra Ehret,Luciana Hannibal,Kai‐Uwe Eckardt,Carola Hunte,Björn Neubauer,Anna Köttgen,Michael Köttgen
标识
DOI:10.1016/j.kint.2024.06.022
摘要
Choline has important physiological functions as a precursor for essential cell components, signaling molecules, phospholipids, and the neurotransmitter acetylcholine. Choline is a water-soluble charged molecule requiring transport proteins to cross biological membranes. Although transporters continue to be identified, membrane transport of choline is incompletely understood and knowledge about choline transport into intracellular organelles such as mitochondria remains limited. Here we show that SLC25A48 imports choline into human mitochondria. Human loss-of-function mutations in SLC25A48 show impaired choline transport into mitochondria and are associated with elevated urine and plasma choline levels. Thus, our studies may have implications for understanding and treating conditions related to choline metabolism.
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