PDGF receptor β signaling in pericytes following ischemic brain injury

Curr Neurovasc Res. 2012 Feb;9(1):1-9. doi: 10.2174/156720212799297100.

Abstract

Platelet derived growth factor (PDGF)-B plays a neuroprotective role in brain damages, including ischemic stroke. It has been suggested recently that PDGF receptor β (PDGFRβ) expressed in brain pericytes as well as in neurons and astrocytes may mediate the neuroprotective role of PDGF-B. The aims of this study were to elucidate the roles of PDGFRβ signaling in brain pericytes after ischemic stroke. In a rat middle cerebral artery occlusion (MCAO) model, PDGFRβ expression was induced specifically in the pericytes in peri-infarct areas and its level was gradually increased. PDGF-B induced marked phosphorylation of Akt in cultured brain pericytes. Consistently, PDGF-B was upregulated in endothelial cells in per-infarct areas and Akt was strongly phosphorylated in the PDGFRβ-expressing pericytes in periinfarct areas after MCAO. In the cultured pericytes, PDGF-B induced cell growth and anti-apoptotic responses through Akt. Furthermore, PDGF-B significantly increased the expression of nerve growth factor (NGF) and neurotrophin-3 (NT-3) through Akt in the pericytes. Thus, the PDGFRβ-Akt signaling in brain pericytes may play various important roles leading to neuroprotection after ischemic stroke.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain Ischemia / metabolism*
  • Disease Models, Animal
  • Fluorescent Antibody Technique
  • Immunoblotting
  • Immunohistochemistry
  • Pericytes / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Rats
  • Real-Time Polymerase Chain Reaction
  • Receptor, Platelet-Derived Growth Factor beta / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction / physiology*
  • Up-Regulation

Substances

  • Receptor, Platelet-Derived Growth Factor beta
  • Proto-Oncogene Proteins c-akt