Molecular basis of hereditary iron homeostasis defects

Hematology. 2010 Apr;15(2):96-111. doi: 10.1179/102453310X12583347009810.

Abstract

Iron is a trace element that is vital for life. It is a component of innumerable hemoproteins and many essential non-heme iron proteins that are involved in oxygen binding and metabolism and electron transfer. Nevertheless, iron can also be toxic to cells as it catalyses the production of oxygen radicals. Iron uptake, transport, storage and utilization are therefore strictly regulated to meet the body's iron needs and to avoid its potential toxicity. Any imbalance in iron homeostasis may lead to the development of pathological conditions associated with either iron overload or iron deficiency. In this paper, we review the current understanding of iron biology with a focus on erythroid iron demand. In addition, we will discuss molecular pathophysiology with implications for novel therapies of selected hereditary defects of iron homeostasis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antimicrobial Cationic Peptides / physiology
  • Biological Transport
  • Duodenum / physiology
  • Enterocytes / metabolism
  • Erythroid Cells / metabolism
  • Erythropoiesis / physiology
  • Hemeproteins / physiology
  • Hepcidins
  • Homeostasis / genetics
  • Homeostasis / physiology*
  • Humans
  • Intestinal Absorption
  • Iron / metabolism*
  • Iron Deficiencies
  • Iron Overload / metabolism
  • Iron, Dietary / pharmacokinetics
  • Iron-Binding Proteins / physiology
  • Macrophages / metabolism
  • Metal Metabolism, Inborn Errors / genetics
  • Metal Metabolism, Inborn Errors / metabolism
  • Mice
  • Mice, Knockout
  • Nonheme Iron Proteins / physiology
  • Oxygen / blood
  • Oxygen / metabolism

Substances

  • Antimicrobial Cationic Peptides
  • Hemeproteins
  • Hepcidins
  • Iron, Dietary
  • Iron-Binding Proteins
  • Nonheme Iron Proteins
  • Iron
  • Oxygen