HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

The mutual crosstalk between iron and erythropoiesis.

Abstract
Iron homeostasis and erythropoiesis are strongly interconnected. On one side iron is essential to terminal erythropoiesis for hemoglobin production, on the other erythropoiesis may increase iron absorption through the production of erythroferrone, the erythroid hormone that suppresses hepcidin expression Also erythropoietin production is modulated by iron through the iron regulatory proteins-iron responsive elements that control the hypoxia inducible factor 2-α. The second transferrin receptor, an iron sensor both in the liver and in erythroid cells modulates erythropoietin sensitivity and is a further link between hepcidin and erythropoiesis. When erythropoietin is decreased in iron deficiency the erythropoietin sensitivity is increased because the second transferrin receptor is removed from cell surface. A deranged balance between erythropoiesis and iron/hepcidin may lead to anemia, as in the case of iron deficiency, defective iron uptake and erythroid utilization or subnormal recycling. Defective control of hepcidin production may cause iron deficiency, as in the recessive disorder iron refractory iron deficiency anemia or in anemia of inflammation, or in iron loading anemias, which are characterized by excessive but ineffective erythropoiesis. The elucidation of the mechanisms that regulates iron homeostasis and erythropoiesis is leading to the development of drugs for the benefit of both iron and erythropoiesis disorders.
AuthorsClara Camaschella, Alessia Pagani, Laura Silvestri, Antonella Nai
JournalInternational journal of hematology (Int J Hematol) Vol. 116 Issue 2 Pg. 182-191 (Aug 2022) ISSN: 1865-3774 [Electronic] Japan
PMID35618957 (Publication Type: Journal Article, Review)
Copyright© 2022. Japanese Society of Hematology.
Chemical References
  • Hepcidins
  • Receptors, Transferrin
  • Erythropoietin
  • Iron
Topics
  • Anemia (etiology, metabolism)
  • Erythropoiesis (physiology)
  • Erythropoietin (pharmacology)
  • Hepcidins (metabolism)
  • Humans
  • Iron (metabolism)
  • Iron Deficiencies (etiology, metabolism)
  • Receptors, Transferrin
  • Signal Transduction

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: