Astrocytes: regulation of brain homeostasis via apolipoprotein E

Int J Biochem Cell Biol. 2005 Jun;37(6):1145-50. doi: 10.1016/j.biocel.2004.10.004.

Abstract

Astrocytes are derived from the ventricular and subventricular zones of the neural plate, though there is controversy over their derivation from astrocyte-specific precursor cells or radial glia intermediates. Astrocytes are the most abundant cell type in the brain and contribute to brain homeostasis in several ways, including buffering of extracellular K+, regulating neurotransmitter release, forming the blood-brain barrier (BBB), releasing growth factors, and regulating the brain immune response. In addition, astrocytes have been shown to release apolipoprotein E (ApoE), which has been shown to regulate neurotransmission, growth factor release, and immune responses. Due to the diverse functions of astrocytes, they may play a role in a variety of diseases such as hepatic encephalopathy, multiple sclerosis, epilepsy, and age-related diseases including Alzheimer's disease and Parkinson's disease. This review highlights many of the diverse roles played by astrocytes in regulating brain homeostasis and discusses their potential role in a variety of disorders.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Animals
  • Apolipoproteins E / biosynthesis
  • Apolipoproteins E / physiology*
  • Astrocytes / physiology*
  • Blood-Brain Barrier / physiology
  • Brain / physiology*
  • Encephalitis / physiopathology
  • Homeostasis / physiology*
  • Humans
  • Neurotransmitter Agents / metabolism
  • Potassium / metabolism

Substances

  • Apolipoproteins E
  • Neurotransmitter Agents
  • Potassium