Department of Food and Nutrition, Faculty of Home Economics, Kyoto Women's University, Kyoto 605-8501, Japan.
Department of Pharmacy, The University of Tokyo Hospital, Faculty of Medicine, The University of Tokyo, Tokyo 113-8655, Japan.
Nutrients. 2023 Feb 16;15(4):998. doi: 10.3390/nu15040998.
ATP-binding cassette protein G5 (ABCG5)/ABCG8 heterodimer exports cholesterol from cells, while Niemann-Pick C1-like 1 (NPC1L1) imports cholesterol and vitamin K. We examined whether ABCG5/ABCG8 transports vitamin K similar to NPC1L1. Since high concentrations of vitamin K show cytotoxicity, the cytoprotective effects of ABCG5/ABCG8 were examined. BHK cells expressing ABCG5/ABCG8 were more resistant to vitamin K cytotoxicity than control cells, suggesting that ABCG5/ABCG8 transports vitamin K out of cells. The addition of vitamin K reversed the effects of ABCG5/ABCG8, suggesting that vitamin K competitively inhibits the transport of vitamin K. To examine the transport of vitamin K by ABCG5/ABCG8, vitamin K levels in the medium and cells were measured. Vitamin K levels in cells expressing ABCG5/ABCG8 were lower than those in control cells, while vitamin K efflux increased in cells expressing ABCG5/ABCG8. Furthermore, the biliary vitamin K concentration in Abcg5/Abcg8-deficient mice was lower than that in wild-type mice, although serum vitamin K levels were not affected by the presence of Abcg5/Abcg8. These findings suggest that ABCG5 and ABCG8 are involved in the transport of sterols and vitamin K. ABCG5/ABCG8 and NPC1L1 might play important roles in the regulation of vitamin K absorption and excretion.
三磷酸腺苷结合盒蛋白 G5(ABCG5)/ABCG8 异二聚体将胆固醇从细胞内排出,而 Niemann-Pick C1 样 1(NPC1L1)则将胆固醇和维生素 K 摄入细胞内。我们研究了 ABCG5/ABCG8 是否像 NPC1L1 一样转运维生素 K。由于高浓度的维生素 K 具有细胞毒性,因此研究了 ABCG5/ABCG8 的细胞保护作用。表达 ABCG5/ABCG8 的 BHK 细胞比对照细胞对维生素 K 的细胞毒性更具抗性,这表明 ABCG5/ABCG8 将维生素 K 从细胞内转运出去。添加维生素 K 可逆转 ABCG5/ABCG8 的作用,表明维生素 K 竞争性抑制维生素 K 的转运。为了研究 ABCG5/ABCG8 对维生素 K 的转运作用,我们测量了培养基和细胞中的维生素 K 水平。表达 ABCG5/ABCG8 的细胞中的维生素 K 水平低于对照细胞,而表达 ABCG5/ABCG8 的细胞中维生素 K 外流增加。此外,Abcg5/Abcg8 缺陷型小鼠的胆汁中维生素 K 浓度低于野生型小鼠,尽管血清维生素 K 水平不受 Abcg5/Abcg8 的影响。这些发现表明 ABCG5 和 ABCG8 参与了固醇和维生素 K 的转运。ABCG5/ABCG8 和 NPC1L1 可能在维生素 K 吸收和排泄的调节中发挥重要作用。