Slc11a2 is required for intestinal iron absorption and erythropoiesis but dispensable in placenta and liver

作者：Hiromi Gunshin, Yuko Fujiwara, Ángel O. Custodio, Cristina DiRenzo, Sylvie Robine, Nancy C. Andrews · 发表于：Journal of Clinical Investigation · 年份：2005 · DOI：10.1172/jci24356 · 被引用次数：415 · 研究领域：Iron Metabolism and Disorders、Hemoglobinopathies and Related Disorders、Trace Elements in Health

Solute carrier family 11, member 2 (SLC11A2) is the only transmembrane iron transporter known to be involved in cellular iron uptake. It is widely expressed and has been postulated to play important roles in intestinal iron absorption, erythroid iron utilization, hepatic iron accumulation, placental iron transfer, and other processes. Previous studies have suggested that other transporters might exist, but their physiological significance remained uncertain. To define the activities of Slc11a2 in vivo, we inactivated the murine gene that encodes it globally and selectively. We found that fetal Slc11a2 is not needed for materno-fetal iron transfer but that Slc11a2 activity is essential for intestinal non-heme iron absorption after birth. Slc11a2 is also required for normal hemoglobin production during the development of erythroid precursors. However, hepatocytes and most other cells must have an alternative, as-yet-unknown, iron uptake mechanism. We previously showed that Slc11a2 serves as the primary portal for intestinal iron entry in hemochromatosis. However, inactivation of murine Hfe ameliorates the phenotype of animals lacking Slc11a2.