Molecular regulation of cellular iron balance

IUBMB Life. 2017 Jun;69(6):389-398. doi: 10.1002/iub.1628. Epub 2017 May 7.

Abstract

Handling a life-supporting yet redox-active metal like iron represents a significant challenge to cells and organisms that must not only tightly balance intra- and extracellular iron concentrations but also chaperone it during its journey from its point of entry to final destinations, to prevent inappropriate generation of damaging reactive oxygen species. Accordingly, regulatory mechanisms have been developed to maintain appropriate cellular and body iron levels. In intracellular compartments, about 95% of iron is protein-bound and the expression of the major proteins of iron metabolism is controlled by an integrated and dynamic system involving multilayered levels of regulation. However, dysregulation of iron homeostasis, which could result from both iron-related and unrelated effectors, may occur and have important pathological consequences in a number of human disorders. In this review, we describe the current understanding of the mechanisms that keep cellular iron balance and outline recent advances that increased our knowledge of the molecular physiology of iron metabolism. © 2017 IUBMB Life, 69(6):389-398, 2017.

Keywords: ferritin; ferroportin; hepcidin; iron; iron regulatory proteins; transferrin receptor.

Publication types

  • Review

MeSH terms

  • Animals
  • Antigens, CD / genetics*
  • Antigens, CD / metabolism
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Cation Transport Proteins / genetics
  • Cation Transport Proteins / metabolism
  • DNA-Binding Proteins
  • Ferritins / genetics*
  • Ferritins / metabolism
  • Gene Expression Regulation*
  • Hemeproteins / genetics
  • Hemeproteins / metabolism
  • Hepcidins / genetics
  • Hepcidins / metabolism
  • Heterogeneous-Nuclear Ribonucleoproteins / genetics
  • Heterogeneous-Nuclear Ribonucleoproteins / metabolism
  • Homeostasis / genetics
  • Humans
  • Iron / metabolism*
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • RNA-Binding Proteins
  • Receptors, Transferrin / genetics*
  • Receptors, Transferrin / metabolism
  • Response Elements
  • Signal Transduction
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Transferrin / genetics*
  • Transferrin / metabolism

Substances

  • Antigens, CD
  • Basic Helix-Loop-Helix Transcription Factors
  • CD71 antigen
  • Cation Transport Proteins
  • DMRT1 protein
  • DNA-Binding Proteins
  • HAMP protein, human
  • Hemeproteins
  • Hepcidins
  • Heterogeneous-Nuclear Ribonucleoproteins
  • PCBP1 protein, human
  • Protein Isoforms
  • RNA-Binding Proteins
  • Receptors, Transferrin
  • SLC48A1 protein, human
  • Transcription Factors
  • Transferrin
  • metal transporting protein 1
  • endothelial PAS domain-containing protein 1
  • Ferritins
  • Iron