Iron Genes and Immune System (IRIS), Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Am J Physiol Gastrointest Liver Physiol. 2010 Apr;298(4):G525-9. doi: 10.1152/ajpgi.00449.2009. Epub 2010 Jan 28.
Hereditary hemochromatosis (HH), a widespread hereditary iron metabolism disorder, is characterized by an excessive absorption of dietary iron, resulting in increased body iron stores. Some studies indicate a sex difference in disease expression, with women showing a slower disease progression and a less severe clinical profile. This is usually attributed to iron loss during menstruation and pregnancy. However, this link has not been clearly demonstrated. The Hfe-/- mouse model recapitulates key aspects of HH, including an iron overload phenotype similar to that observed in human patients. In this study, we use it to test the impact of multiple pregnancies in the iron stores. One-year-old nulliparous and pluriparous (averaging 29 weaned pups per female) C57BL/6 (B6) and Hfe-/- mice were euthanized, and blood and tissues were collected. Several serological and erythroid parameters were evaluated, as well as tissue nonheme iron content and serum ferritin. Hepcidin 1, hepcidin 2, and bone morphogenetic protein 6 (BMP6) expressions in the liver were determined by real-time PCR. No significant differences were observed for many serological and erythroid parameters although differences occurred in transferrin saturation and mean corpuscular volume in Hfe-/- mice and total iron-binding capacity in B6 mice. Hepatic iron concentration was similar for nulliparous and pluriparous mice of both genotypes, but total iron per organ (liver, spleen, heart, and pancreas) was higher overall in pluriparous females than nulliparous. Hepcidin 1 and 2 and BMP6 expressions were significantly decreased in pluriparous females, when compared with nulliparous, in both genotypes. In conclusion, multiple pregnancies do not reduce body iron stores in Hfe-/- mice.
遗传性血色素沉着症(HH)是一种广泛存在的遗传性铁代谢紊乱,其特征是对膳食铁的过度吸收,导致体内铁储存增加。一些研究表明,疾病的表达存在性别差异,女性的疾病进展较慢,临床表现较轻。这通常归因于月经和妊娠期间的铁丢失。然而,这一联系尚未得到明确证实。Hfe-/-小鼠模型再现了 HH 的关键方面,包括类似于人类患者的铁过载表型。在这项研究中,我们使用它来测试多次妊娠对铁储存的影响。对 1 岁的未产和多产(平均每只雌性产 29 只断奶幼崽)C57BL/6(B6)和 Hfe-/-小鼠进行安乐死,并收集血液和组织。评估了几项血清学和红细胞参数,以及组织非血红素铁含量和血清铁蛋白。通过实时 PCR 测定肝脏中hepcidin 1、hepcidin 2 和骨形态发生蛋白 6(BMP6)的表达。尽管 Hfe-/- 小鼠的转铁蛋白饱和度和平均红细胞体积以及 B6 小鼠的总铁结合能力存在差异,但许多血清学和红细胞参数没有差异。未产和多产的两种基因型的小鼠肝脏铁浓度相似,但多产雌鼠的每个器官(肝、脾、心和胰腺)的总铁含量总体上更高。与未产相比,多产雌鼠的 hepcidin 1 和 2 以及 BMP6 的表达均显著降低,两种基因型均如此。总之,多次妊娠不会减少 Hfe-/- 小鼠体内的铁储存。