Details
- Autor(en) / Beteiligte
- Titel
- Neogenin inhibits HJV secretion and regulates BMP-induced hepcidin expression and iron homeostasis
- Ist Teil von
- Blood, 2010-04, Vol.115 (15), p.3136-3145
- Ort / Verlag
- Washington, DC: Elsevier Inc
- Erscheinungsjahr
- 2010
- Link zum Volltext
- Quelle
- Alma/SFX Local Collection
- Beschreibungen/Notizen
- Neogenin, a deleted in colorectal cancer (DCC) family member, has been identified as a receptor for the neuronal axon guidance cues netrins and repulsive guidance molecules repulsive guidance molecules (RGM). RGMc, also called hemojuvelin (HJV), is essential for iron homeostasis. Here we provide evidence that neogenin plays a critical role in iron homeostasis by regulation of HJV secretion and bone morphogenetic protein (BMP) signaling. Livers of neogenin mutant mice exhibit iron overload, low levels of hepcidin, and reduced BMP signaling. Mutant hepatocytes in vitro show impaired BMP2 induction of Smad1/5/8 phosphorylation and hepcidin expression. Neogenin is expressed in liver cells in a reciprocal pattern to that of hepcidin, suggesting that neogenin functions in a cell nonautonomous manner. Further studies demonstrate that neogenin may stabilize HJV, a glycosylphosphatidylinositol-anchored protein that interacts with neogenin and suppresses its secretion. Taken together, our results lead the hypothesis that neogenin regulates iron homeostasis via inhibiting secretion of HJV, an inhibitor of BMP signaling, to enhance BMP signaling and hepcidin expression. These results reveal a novel mechanism underlying neogenin regulation of HJV-BMP signaling.
- Sprache
- Englisch
- Identifikatoren
- ISSN: 0006-4971eISSN: 1528-0020DOI: 10.1182/blood-2009-11-251199Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2858467
- Format
- –
- Schlagworte
- Animals, Antimicrobial Cationic Peptides - genetics, Antimicrobial Cationic Peptides - metabolism, Biological and medical sciences, Bone Morphogenetic Protein 2 - pharmacology, Cation Transport Proteins - metabolism, Extracellular Space - drug effects, Extracellular Space - metabolism, Gene Expression Regulation - drug effects, GPI-Linked Proteins, Hematologic and hematopoietic diseases, Hemochromatosis Protein, Hep G2 Cells, Hepatocytes - drug effects, Hepatocytes - metabolism, Hepatocytes - pathology, Hepcidins, Homeostasis - drug effects, Humans, Iron - metabolism, Iron Overload - genetics, Iron Overload - pathology, Liver - drug effects, Liver - metabolism, Liver - pathology, Medical sciences, Membrane Proteins - deficiency, Membrane Proteins - genetics, Membrane Proteins - metabolism, Mice, Mice, Inbred C57BL, Mice, Mutant Strains, Phosphorylation - drug effects, Protein Transport - drug effects, Red Cells, Iron, and Erythropoiesis, Signal Transduction - drug effects, Smad Proteins - metabolism