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Out of Balance-Systemic Iron Homeostasis in Iron-Related Disorders

Journal

NUTRIENTS
Volume 5, Issue 8, Pages 3034-3061

Publisher

MDPI
DOI: 10.3390/nu5083034

Keywords

iron regulation; hepcidin; anemia; iron overload

Funding

  1. Muenster University [IMF ST-111206]
  2. Dietmar Hopp Stiftung
  3. eRARE HMAIRON
  4. Deutsche Forschungsgemeinschaft [SFB 1036, TP16]
  5. German Federal Ministry of Education and Research (BMBF) [82DZL00401]
  6. BMBF

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Iron is an essential element in our daily diet. Most iron is required for the de novo synthesis of red blood cells, where it plays a critical role in oxygen binding to hemoglobin. Thus, iron deficiency causes anemia, a major public health burden worldwide. On the other extreme, iron accumulation in critical organs such as liver, heart, and pancreas causes organ dysfunction due to the generation of oxidative stress. Therefore, systemic iron levels must be tightly balanced. Here we focus on the regulatory role of the hepcidin/ferroportin circuitry as the major regulator of systemic iron homeostasis. We discuss how regulatory cues (e. g., iron, inflammation, or hypoxia) affect the hepcidin response and how impairment of the hepcidin/ferroportin regulatory system causes disorders of iron metabolism.

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