Food Science and Human Nutrition Department, University of Florida, Gainesville, Florida, United States of America.
PLoS One. 2013 Jun 11;8(6):e66010. doi: 10.1371/journal.pone.0066010. Print 2013.
During iron deficiency, perturbations in copper homeostasis have frequently been documented. Previous studies in iron-deprived rats demonstrated that enterocyte and hepatic copper levels increase and a copper transporter (the Menkes Copper ATPase; Atp7a) is induced in the duodenal epithelium in parallel to iron transport-related genes (e.g. Dmt1, Dcytb, Fpn1). Moreover, two ferroxidase proteins involved in iron homeostasis, hephaestin expressed in enterocytes and ceruloplasmin, produced and secreted into blood by the liver, are copper-dependent enzymes. We thus aimed to test the hypothesis that Atp7a function is important for the copper-related compensatory response of the intestinal epithelium to iron deficiency. Accordingly, iron homeostasis was studied for the first time in mice expressing a mutant Atp7a protein with minimal activity (Brindled [Mo (Br) (/y) ]). Mutant mice were rescued by perinatal copper injections, and, after a 7-8 week recovery period, were deprived of dietary iron for 3 weeks (along with WT littermates). Adult Mo (Br) (/y) mice displayed copper-deficiency anemia but had normal iron status; in contrast, iron-deprived Mo (Br) (/y) mice were iron deficient and more severely anemic with partial amelioration of the copper-deficient phenotype. Intestinal iron absorption in both genotypes (WT and Mo (Br) (/y) ) increased ∼3-fold when mice consumed a low-iron diet and ∼6-fold when mice were concurrently bled. WT mice exhibited no alterations in copper homeostasis in response to iron deprivation or phlebotomy. Conversely, upregulation of iron absorption was associated with increased enterocyte and liver copper levels and serum ferroxidase (ceruloplasmin) activity in Mo (Br) (/y) mice, typifying the response to iron deprivation in many mammalian species. We thus speculate that a copper threshold exists that is necessary to allow appropriate regulate of iron absorption. In summary, Mo (Br) (/y) mice were able to adequately regulate iron absorption, but unlike in WT mice, concurrent increases in enterocyte and liver copper levels and serum ferroxidase activity may have contributed to maintenance of iron homeostasis.
在缺铁时,铜稳态的紊乱经常被记录下来。以前在缺铁的大鼠中进行的研究表明,肠细胞和肝铜水平增加,并且在十二指肠上皮中与铁转运相关基因(例如 Dmt1、Dcytb、Fpn1)平行诱导一种铜转运体(Menkes 铜 ATP 酶;Atp7a)。此外,两种参与铁稳态的亚铁氧化酶蛋白,在肠细胞中表达的 hephaestin 和由肝脏产生并分泌到血液中的 ceruloplasmin,是依赖铜的酶。因此,我们旨在测试 Atp7a 功能对于肠道上皮对缺铁的铜相关补偿反应的重要性的假设。因此,首次在表达具有最小活性的突变 Atp7a 蛋白的小鼠中研究了铁稳态(斑驳[Mo(Br)(/ y)])。突变小鼠通过围产期铜注射得到挽救,并且在 7-8 周的恢复期后,用缺乏饮食铁处理 3 周(与 WT 同窝仔鼠一起)。成年 Mo(Br)(/ y)小鼠表现出铜缺乏性贫血,但铁状态正常;相比之下,缺铁的 Mo(Br)(/ y)小鼠缺铁且贫血更严重,铜缺乏表型部分改善。当两种基因型(WT 和 Mo(Br)(/ y))的小鼠消耗低铁饮食时,肠道铁吸收增加约 3 倍,当同时放血时增加约 6 倍。WT 小鼠在缺铁或放血时,铜稳态没有变化。相反,铁吸收的上调与 Mo(Br)(/ y)小鼠的肠细胞和肝脏铜水平以及血清亚铁氧化酶(ceruloplasmin)活性增加有关,这是许多哺乳动物物种对缺铁的反应。因此,我们推测存在一个铜阈值,这是适当调节铁吸收所必需的。总之,Mo(Br)(/ y)小鼠能够充分调节铁吸收,但是与 WT 小鼠不同,肠细胞和肝脏铜水平以及血清亚铁氧化酶活性的同时增加可能有助于维持铁稳态。