D'Anna María Cecilia, Veuthey Tania Vanesa, Roque Marta Elena
Laboratory of Human Physiology, Department of Biology, Biochemistry, and Pharmacy, Universidad Nacional del Sur, San Juan 670, Bahía Blanca, Argentina.
J Histochem Cytochem. 2009 Jan;57(1):9-16. doi: 10.1369/jhc.2008.951616. Epub 2008 Sep 15.
Ferroportin (FPN), the only iron exporter identified to date, participates in iron release from enterocytes and macrophages, regulating its absorption and recycling. We used a murine model of experimental hemolytic anemia to study adaptive changes in the localization of FPN in duodenum, liver, and spleen. FPN was assessed by IHC in healthy and anemic mice using rabbit anti-mouse FPN polyclonal antibodies. Goat-labeled polymer-horseradish peroxidase anti-rabbit Envision+System (DAB) was used as secondary antibody. Tissue iron was studied by Prussian blue iron staining. Anemia evolution and erythropoietic recovery was assessed using conventional hematological tests. Healthy mice showed mainly supranuclear expression of FPN in enterocytes and a weak basolateral expression, whereas in anemic mice, the expression was detected mainly at the basolateral membrane (days 4 and 5). Red pulp macrophages of healthy mice showed FPN-hemosiderin colocalization. In the liver of healthy mice, FPN was mainly cytoplasmic, whereas in anemic mice, it was redistributed to the cell membrane. Our findings clearly show that anemia induces adaptive changes in FPN expression, contributing to anemia restoration by increasing available iron. FPN expression in the membrane is the main pathway of iron release. Our data indicate that iron homeostasis in vivo is maintained through the coordinated expression of this iron exporter in both intestinal and phagocytic cells.
铁转运蛋白(FPN)是迄今为止发现的唯一一种铁输出蛋白,参与肠上皮细胞和巨噬细胞释放铁,调节铁的吸收和再循环。我们使用实验性溶血性贫血小鼠模型来研究十二指肠、肝脏和脾脏中FPN定位的适应性变化。使用兔抗小鼠FPN多克隆抗体通过免疫组化法在健康小鼠和贫血小鼠中评估FPN。使用山羊标记的聚合物辣根过氧化物酶抗兔Envision +系统(DAB)作为二抗。通过普鲁士蓝铁染色研究组织铁。使用常规血液学检测评估贫血的进展和红细胞生成的恢复。健康小鼠的肠上皮细胞中FPN主要在核上表达,基底外侧表达较弱,而在贫血小鼠中,表达主要在基底外侧膜检测到(第4天和第5天)。健康小鼠的脾髓巨噬细胞显示FPN-含铁血黄素共定位。在健康小鼠的肝脏中,FPN主要位于细胞质中,而在贫血小鼠中,它重新分布到细胞膜上。我们的研究结果清楚地表明,贫血诱导FPN表达的适应性变化,通过增加可利用的铁来促进贫血的恢复。膜中FPN的表达是铁释放的主要途径。我们的数据表明,体内铁稳态是通过这种铁输出蛋白在肠道和吞噬细胞中的协调表达来维持的。