Agata Tarczykowska, Per Malmberg, Nathalie Scheers
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Iron uptake (ferritin L) from ferrous fumarate (0.5 mM, 24 h) in DMT1 silenced cells was significantly decreased (60% ± 11%) in comparison to iron controls while a 1-h dose of ferrous fumarate (0.5 mM) significantly decreased ferritin L formation in the presence of the clathrin inhibitor chlorpromazine (61% ± 10%, in post-confluent cells and 37% ± 9% in non-confluent cells). A pilot showed a similar trend for Ferritin (H) levels (confluent cells) and for total cellular iron load (non-confluent cells). ToF-SIMS analysis revealed diminished membrane-associated iron load in endocytosis-inhibited ferrous fumarate treated cells. The reported results support a clathrin-mediated endocytosis mechanism for uptake of iron from ferrous fumarate in addition to iron uptake by DMT1. 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A pilot showed a similar trend for Ferritin (H) levels (confluent cells) and for total cellular iron load (non-confluent cells). ToF-SIMS analysis revealed diminished membrane-associated iron load in endocytosis-inhibited ferrous fumarate treated cells. The reported results support a clathrin-mediated endocytosis mechanism for uptake of iron from ferrous fumarate in addition to iron uptake by DMT1. 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引用次数: 0
摘要
肠上皮的铁摄取与通过DMT1转运体(SLC11a2;NRAMP2)。在后来的几年里,从复杂的来源,如纳米颗粒,铁的摄取被发现是通过内吞作用介导的。在这里,我们提出单盐富马酸亚铁中的铁,一种常见的铁补充剂,可以通过网格蛋白介导的内吞作用被吸收。我们使用siRNA沉默DMT1转运蛋白表达,药理抑制内吞作用,并使用飞行时间二次离子质谱(ToF-SIMS)来证明胡图-80细胞中富马酸亚铁的铁摄取既可以通过DMT1转运,也可以通过网状蛋白依赖的内吞作用介导。与铁对照组相比,DMT1沉默细胞中富马酸亚铁(0.5 mM, 24 h)对铁的摄取(铁蛋白L)显著降低(60%±11%),而1小时剂量的富马酸亚铁(0.5 mM)在clathrin抑制剂氯丙丙存在下显著降低铁蛋白L的形成(61%±10%,在融合后细胞中,37%±9%,在非融合细胞中)。一项试验显示,铁蛋白(H)水平(融合细胞)和细胞总铁负荷(非融合细胞)也有类似的趋势。ToF-SIMS分析显示,在内吞抑制富马酸亚铁处理的细胞中,膜相关铁负荷减少。报道的结果支持一个网格蛋白介导的内吞机制,从富马酸亚铁中摄取铁,以及由DMT1摄取铁。需要更多的研究来了解是什么决定了哪种摄取机制以及在何种程度上被采用。
Uptake of iron from ferrous fumarate can be mediated by clathrin-dependent endocytosis in Hutu-80 cells.
Iron uptake in the intestinal epithelium is associated with transport of ferrous iron via the DMT1 transporter (SLC11a2; NRAMP2). In later years, uptake of iron from complex sources, such as nanoparticles, has been found to be mediated through endocytosis. Here we propose that iron from the simple salt ferrous fumarate, a common iron supplement, can be absorbed by clathrin-mediated endocytosis. We used siRNA to silence DMT1 transporter expression, pharmacological inhibition of endocytosis, and Time-of-Flight Secondary Ion Mass Spectrometry (ToF-SIMS) to show that iron uptake from ferrous fumarate can be mediated by both transport via DMT1 and by clathrin-dependent endocytosis in Hutu-80 cells. Iron uptake (ferritin L) from ferrous fumarate (0.5 mM, 24 h) in DMT1 silenced cells was significantly decreased (60% ± 11%) in comparison to iron controls while a 1-h dose of ferrous fumarate (0.5 mM) significantly decreased ferritin L formation in the presence of the clathrin inhibitor chlorpromazine (61% ± 10%, in post-confluent cells and 37% ± 9% in non-confluent cells). A pilot showed a similar trend for Ferritin (H) levels (confluent cells) and for total cellular iron load (non-confluent cells). ToF-SIMS analysis revealed diminished membrane-associated iron load in endocytosis-inhibited ferrous fumarate treated cells. The reported results support a clathrin-mediated endocytosis mechanism for uptake of iron from ferrous fumarate in addition to iron uptake by DMT1. More studies are needed to understand what determines which uptake mechanism are employed and to which extent.
期刊介绍:
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