Iron dysregulation and neurodegeneration: the molecular connection

Mol Interv. 2006 Apr;6(2):89-97. doi: 10.1124/mi.6.2.6.

Abstract

Iron is essential for many biological processes however excess concentrations can be harmful to many tissues. Its amounts must therefore be carefully regulated in all cells of the body including those in the brain. Increased amounts of iron have been reported in many neurodegenerative disorders. Whether this increased iron contributes to neurodegeneration has been considered controversial. In this review, we discuss some recently identified anomalies in proteins linked with iron metabolism which signify a critical role for iron dysregulation in neurodegeneration.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cation Transport Proteins / genetics
  • Cation Transport Proteins / metabolism
  • Ceruloplasmin / genetics
  • Ceruloplasmin / metabolism
  • Frataxin
  • Heme Oxygenase-1 / metabolism
  • Hemochromatosis Protein
  • Histocompatibility Antigens Class I / genetics
  • Histocompatibility Antigens Class I / metabolism
  • Humans
  • Iron / metabolism*
  • Iron Metabolism Disorders
  • Iron-Binding Proteins / genetics
  • Iron-Binding Proteins / metabolism
  • Iron-Regulatory Proteins / metabolism*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Metalloproteins / genetics
  • Metalloproteins / metabolism
  • Mice
  • Mice, Transgenic
  • Models, Biological
  • Mutation
  • Nerve Degeneration / genetics*
  • Neurodegenerative Diseases / etiology*
  • Neurodegenerative Diseases / genetics
  • Neurodegenerative Diseases / metabolism*
  • Phosphotransferases (Alcohol Group Acceptor) / genetics
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism

Substances

  • Cation Transport Proteins
  • HFE protein, human
  • Hemochromatosis Protein
  • Histocompatibility Antigens Class I
  • Iron-Binding Proteins
  • Iron-Regulatory Proteins
  • Membrane Proteins
  • Metalloproteins
  • solute carrier family 11- (proton-coupled divalent metal ion transporters), member 2
  • Iron
  • Heme Oxygenase-1
  • Ceruloplasmin
  • Phosphotransferases (Alcohol Group Acceptor)
  • pantothenate kinase