Abstract
Heme-regulated eIF2alpha kinase (HRI) is essential for regulating globin translation in iron deficiency and in beta-thalassemia. We investigated the role of heme-regulated eIF2alpha kinase in hemoglobin and red blood cell production as well as in iron homeostasis in a mouse model of iron overload. We show that HRI deficiency does not significantly affect red cell parameters of hemochromatosis (HFE(-)(/)(-)) mice. Importantly, heme-regulated eIF2alpha kinase deficiency exacerbates decreases in hepcidin expression and splenic macrophage iron in HFE(-)(/)(-) mice. Furthermore, the serum level of bone morphogenic protein 2, which positively regulates hepcidin, is reduced in heme-regulated eIF2alpha kinase deficiency, but not in HFE deficiency.
Publication types
-
Research Support, N.I.H., Extramural
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Antimicrobial Cationic Peptides / biosynthesis*
-
Bone Morphogenetic Protein 2
-
Bone Morphogenetic Proteins / metabolism
-
Disease Models, Animal
-
Genotype
-
Heme / chemistry*
-
Hemochromatosis / genetics*
-
Hepcidins
-
Iron / metabolism
-
Macrophages / metabolism
-
Mice
-
Mice, Inbred C57BL
-
Mice, Transgenic
-
Phenotype
-
Protein Serine-Threonine Kinases / metabolism*
-
Spleen / metabolism
-
Transforming Growth Factor beta / metabolism
-
eIF-2 Kinase / metabolism*
Substances
-
Antimicrobial Cationic Peptides
-
Bmp2 protein, mouse
-
Bone Morphogenetic Protein 2
-
Bone Morphogenetic Proteins
-
Hamp protein, mouse
-
Hepcidins
-
Transforming Growth Factor beta
-
Heme
-
Iron
-
Protein Serine-Threonine Kinases
-
eIF-2 Kinase
-
eIF2alpha kinase, mouse