Edwards J A, Bannerman R M
J Clin Invest. 1970 Oct;49(10):1869-71. doi: 10.1172/JCI106405.
Iron transport by everted duodenal sacs in vitro was studied in mice with sex-linked anemia (gene symbol sla) (an inherited iron deficiency anemia), in normal mice, and in normal mice on iron-deficient and iron supplemented diets. Although the over-all mucosal uptake of iron was the same in sla and normal sacs, transport of iron to the inside of the sac was much decreased in sla. The iron transport defect in sla was emphasized by the fact that genotypically normal mice on an iron-deficient diet demonstrated greatly increased iron transport. Electrophoretic analysis of protein extracted from sla and normal sacs showed only one iron-binding fraction. The sla and normal fractions had the same mobility and corresponded in position to the major band of horse ferritin. It thus appears that the iron deficiency of sla is due to a genetically determined defect in mucosal iron transport and that this defect is not associated with any demonstrable abnormality of a major iron-binding protein.
利用外翻十二指肠囊在体外研究了患有性连锁贫血(基因符号为sla)(一种遗传性缺铁性贫血)的小鼠、正常小鼠以及分别饲喂缺铁和补铁日粮的正常小鼠的铁转运情况。尽管sla小鼠和正常小鼠十二指肠囊对铁的总体黏膜摄取量相同,但sla小鼠中铁向囊内的转运显著减少。缺铁日粮喂养的基因正常小鼠铁转运大幅增加,这一事实凸显了sla小鼠的铁转运缺陷。对sla小鼠和正常小鼠十二指肠囊提取的蛋白质进行电泳分析,结果仅显示出一个铁结合组分。sla小鼠和正常小鼠的组分具有相同的迁移率,且在位置上与马铁蛋白的主要条带相对应。因此,似乎sla小鼠的缺铁是由于黏膜铁转运存在基因决定的缺陷,且该缺陷与任何可证实的主要铁结合蛋白异常无关。