Redox signalling and regulation of the blood-brain barrier

Int J Biochem Cell Biol. 2020 Aug:125:105794. doi: 10.1016/j.biocel.2020.105794. Epub 2020 Jun 17.

Abstract

Neurological disorders are associated with increased oxidative stress. Reactive oxidants damage tissue and promote cell death, but it is apparent that oxidants can have more subtle effects on cell function through the modulation of redox-sensitive signalling pathways. Cells of the blood-brain barrier regulate the brain microenvironment but become dysfunctional during neurological disease. The blood-brain barrier is maintained by many cell types, and is modulated by redox-sensitive pathways, ranging from the cytoskeletal elements responsible for establishing a barrier, to growth factor and cytokine signalling pathways that influence neurovascular cells. During neurological disease, blood-brain barrier cells are exposed to exogenously generated oxidants from immune cells, as well as increasing endogenously oxidant production. These oxidants impair the function of the blood-brain barrier, leading to increased leakage and reduced blood flow. Reducing the impact of oxidants on the function of blood-brain barrier cells may provide new strategies for delaying the progression of neurological disease.

Keywords: Alzheimer’s disease; Blood-brain barrier; Neuroinflammation; Oxidative stress; Redox signalling; Stroke.

Publication types

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

MeSH terms

  • Animals
  • Astrocytes / metabolism
  • Astrocytes / pathology
  • Blood-Brain Barrier / cytology*
  • Blood-Brain Barrier / enzymology
  • Blood-Brain Barrier / metabolism
  • Cell Death / drug effects
  • Endothelial Cells / enzymology
  • Endothelial Cells / metabolism
  • Humans
  • Inflammation / enzymology
  • Inflammation / immunology
  • Inflammation / metabolism*
  • Microglia / enzymology
  • Microglia / metabolism
  • Nervous System Diseases / enzymology
  • Nervous System Diseases / metabolism*
  • Nervous System Diseases / physiopathology
  • Neutrophils / enzymology
  • Neutrophils / metabolism
  • Oxidation-Reduction / drug effects
  • Oxidative Stress / drug effects
  • Oxidative Stress / physiology*
  • Pericytes / enzymology
  • Pericytes / metabolism
  • Pericytes / pathology
  • Signal Transduction / genetics