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首页> 外文期刊>Scientific reports. >RETRACTED ARTICLE: Identification of a novel Na + -coupled Fe 3+ -citrate transport system, distinct from mammalian INDY, for uptake of citrate in mammalian cells
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RETRACTED ARTICLE: Identification of a novel Na + -coupled Fe 3+ -citrate transport system, distinct from mammalian INDY, for uptake of citrate in mammalian cells

机译:收回的文章:鉴定与哺乳动物INDY不同的新型Na +偶联的Fe 3+-柠檬酸盐转运系统,以吸收哺乳动物细胞中的柠檬酸盐

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NaCT is a Na+-coupled transporter for citrate expressed in hepatocytes and neurons. It is the mammalian ortholog of INDY (I’m Not Dead Yet), a transporter which modifies lifespan in Drosophila. Here we describe a hitherto unknown transport system for citrate in mammalian cells. When liver and mammary epithelial cells were pretreated with the iron supplement ferric ammonium citrate (FAC), uptake of citrate increased 10-fold. Iron chelators abrogated the stimulation of citrate uptake in FAC-treated cells. The iron exporter ferroportin had no role in this process. The stimulation of citrate uptake also occurred when Fe3+ was added during uptake without pretreatment. Similarly, uptake of Fe3+ was enhanced by citrate. The Fe3+-citrate uptake was coupled to Na+. This transport system was detectable in primary hepatocytes and neuronal cell lines. The functional features of this citrate transport system distinguish it from NaCT. Loss-of-function mutations in NaCT cause early-onset epilepsy and encephalopathy; the newly discovered Na+-coupled Fe3+-citrate transport system might offer a novel treatment strategy for these patients to deliver citrate into affected neurons independent of NaCT. It also has implications to iron-overload conditions where circulating free iron increases, which would stimulate cellular uptake of citrate and consequently affect multiple metabolic pathways.
机译:NaCT是在肝细胞和神经元中表达的柠檬酸盐的Na +偶联转运蛋白。这是INDY(我还没死)的哺乳动物直系同源物,它是改变果蝇寿命的转运蛋白。在这里,我们描述了迄今未知的哺乳动物细胞中柠檬酸盐的转运系统。当用铁补充柠檬酸铁铵铵(FAC)预处理肝和乳腺上皮细胞时,柠檬酸的摄取增加> 10倍。铁螯合剂消除了FAC处理细胞中柠檬酸盐摄取的刺激。铁出口铁转运蛋白在此过程中没有作用。当在不进行预处理的情况下在摄取过程中添加Fe3 +时,也会刺激柠檬酸盐的摄取。同样,柠檬酸盐可增强Fe3 +的吸收。柠檬酸铁离子的吸收与钠离子耦合。在原代肝细胞和神经元细胞系中可检测到该转运系统。柠檬酸盐转运系统的功能特点使其与NaCT区别开来。 NaCT的功能丧失突变导致早发性癫痫和脑病。新发现的Na +偶联的Fe3 +-柠檬酸盐转运系统可能为这些患者提供一种新颖的治疗策略,以将柠檬酸盐递送到独立于NaCT的受影响神经元中。它还对铁的过量状况有影响,其中循环中的游离铁增加,这将刺激细胞摄取柠檬酸盐,从而影响多种代谢途径。

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