Kuo Y M, Su T, Chen H, Attieh Z, Syed B A, McKie A T, Anderson G J, Gitschier J, Vulpe C D
Departments of Medicine and Pediatrics, University of California-San Francisco, San Francisco, CA 94143-0794, USA.
Gut. 2004 Feb;53(2):201-6. doi: 10.1136/gut.2003.019026.
Hephaestin is a multicopper ferroxidase required for basolateral transport of iron from enterocytes. Sex linked anaemia (sla) mice have a defect in the release of iron from intestinal enterocytes into the circulation due to an interstitial deletion in the hephaestin gene (heph).
We have demonstrated that hephaestin is primarily localised to a supranuclear compartment in both intestinal enterocytes and in cultured cells. In normal intestinal enterocytes, hephaestin was also present on the basolateral surface. In sla mice, hephaestin was present only in the supranuclear compartment. In contrast, the iron permease Ireg1 localised to the basolateral membrane in both control and sla mice.
We suggest that mislocalisation of hephaestin likely contributes to the functional defect in sla intestinal epithelium.
高铁氧化酶是肠细胞将铁从基底外侧转运所必需的多铜铁氧化酶。性连锁贫血(sla)小鼠由于高铁氧化酶基因(heph)的间质缺失,存在肠道肠细胞中铁释放到循环中的缺陷。
我们已经证明,高铁氧化酶主要定位于肠道肠细胞和培养细胞中的核上区室。在正常肠道肠细胞中,高铁氧化酶也存在于基底外侧表面。在sla小鼠中,高铁氧化酶仅存在于核上区室。相比之下,铁通透酶Ireg1在对照小鼠和sla小鼠中均定位于基底外侧膜。
我们认为高铁氧化酶的错误定位可能导致sla肠上皮细胞的功能缺陷。