Thomas C, Oates P S
Physiology School of Biomedical and Chemical Sciences, University of Western Australia, Crawley, Western Australia.
Gut. 2004 Jan;53(1):44-9. doi: 10.1136/gut.53.1.44.
Absorption of non-haeme iron occurs mainly in the duodenum. It involves the divalent metal transporter 1 (DMT1) in the uptake of ferrous Fe(II) iron and the basolateral transporter ferroportin/IREG-1/MTP-1/SLC40A1 in its release. Whether ferroportin functions in this process at other sites in the enterocyte is unknown. In this study the effect of a blocking antibody to ferroportin on the uptake and release of iron was evaluated in enterocyte-like cells (IEC-6 and Caco-2) and in freshly isolated duodenal enterocytes from rats.
Uptake of 1 microM Fe(II) and its release by cells was studied in the presence of the antibody. Ferroportin expression was determined by western blot analysis of duodenal mucosa enriched microvillus membranes, Caco-2 cells, IEC-6 cells, and freshly isolated enterocytes. Immunofluorescent detection of ferroporitn was performed on frozen sections of duodenum from rats with variations in body iron stores.
Ferroportin was expressed in all cell types. In these cells, the antibody significantly reduced (p<0.05) uptake of Fe(II) by 40-50% but had no effect on the release of iron. In Caco-2 cells, Fe(II) uptake was reduced only when the antibody was in contact with the apical membrane. Ferroportin protein was enriched in microvillus membrane preparations. In enterocytes from iron deficient rats, ferroportin was expressed along the brush border where it colocalised with lactase. Ferroportin was seen in the basal cytoplasm and along the basolateral membranes. Iron loading markedly reduced intracellular expression of ferroportin. In Caco-2 cells, ferroportin also localised to the microvillus and lateral and basal membranes.
In addition to release, ferroportin functions in the uptake of iron at the apical membrane, possibly by modulating the activity of DMT1.
非血红素铁的吸收主要发生在十二指肠。这一过程涉及二价金属转运体1(DMT1)摄取亚铁离子(Fe(II))以及基底外侧转运体铁转运蛋白/铁调节蛋白1/金属转运蛋白1/溶质载体家族40成员1(ferroportin/IREG-1/MTP-1/SLC40A1)释放铁。铁转运蛋白在肠上皮细胞的其他部位是否参与这一过程尚不清楚。在本研究中,我们评估了铁转运蛋白阻断抗体对肠上皮样细胞(IEC-6和Caco-2)以及从大鼠新鲜分离的十二指肠上皮细胞中铁摄取和释放的影响。
在抗体存在的情况下研究细胞对1微摩尔Fe(II)的摄取及其释放情况。通过对富含微绒毛膜的十二指肠黏膜、Caco-2细胞、IEC-6细胞以及新鲜分离的上皮细胞进行蛋白质免疫印迹分析来测定铁转运蛋白的表达。对不同机体铁储备状态的大鼠十二指肠冰冻切片进行铁转运蛋白的免疫荧光检测。
铁转运蛋白在所有细胞类型中均有表达。在这些细胞中,该抗体显著降低(p<0.05)Fe(II)的摄取达40%-50%,但对铁的释放没有影响。在Caco-2细胞中,只有当抗体与顶端膜接触时,Fe(II)摄取才会减少。铁转运蛋白在微绒毛膜制剂中含量丰富。在缺铁大鼠的肠上皮细胞中,铁转运蛋白沿刷状缘表达,与乳糖酶共定位。在基底细胞质和基底外侧膜上也可见铁转运蛋白。铁负荷显著降低铁转运蛋白的细胞内表达。在Caco-2细胞中,铁转运蛋白也定位于微绒毛以及外侧和基底膜。
除了释放功能外,铁转运蛋白在顶端膜的铁摄取过程中发挥作用,可能是通过调节DMT1的活性来实现的。