Patil Suraj, Borisov Oleg, Scherer Nora, Wirth Christophe, Schlosser Pascal, Wuttke Matthias, Ehret Sandra, Hannibal Luciana, Eckardt Kai-Uwe, Hunte Carola, Neubauer Björn, Köttgen Anna, Köttgen Michael
Department of Medicine IV-Nephrology and Primary Care, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany; Institute of Genetic Epidemiology, Faculty of Medicine and Medical Center-University of Freiburg, Freiburg, Germany; Spemann Graduate School of Biology and Medicine (SGBM), University of Freiburg, Freiburg, Germany; Faculty of Biology, University of Freiburg, Freiburg, Germany.
Institute of Genetic Epidemiology, Faculty of Medicine and Medical Center-University of Freiburg, Freiburg, Germany.
Kidney Int. 2025 Feb;107(2):296-301. doi: 10.1016/j.kint.2024.06.022. Epub 2024 Jul 29.
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.
胆碱作为必需细胞成分、信号分子、磷脂和神经递质乙酰胆碱的前体,具有重要的生理功能。胆碱是一种水溶性带电分子,需要转运蛋白才能穿过生物膜。尽管转运蛋白不断被发现,但胆碱的膜转运仍未被完全理解,关于胆碱转运到线粒体等细胞内细胞器的知识仍然有限。在这里,我们表明SLC25A48将胆碱导入人线粒体。SLC25A48的人类功能丧失突变显示胆碱向线粒体的转运受损,并与尿液和血浆胆碱水平升高有关。因此,我们的研究可能对理解和治疗与胆碱代谢相关的疾病有启示意义。