The role of integrin alpha(v)beta (8) in neonatal hypoxic-ischemic brain injury

Neurotox Res. 2010 May;17(4):406-17. doi: 10.1007/s12640-009-9117-y. Epub 2009 Sep 23.

Abstract

Integrin alpha(v)beta(8) plays an important role in cerebral vascular development. It has been proven that alpha(v)beta(8) is a key factor for transforming growth factor-beta1 (TGF-beta1) activation in epithelial cells. However, it is not clear whether alpha(v)beta(8) can activate TGF-beta1 and play a role in protection during neonatal hypoxic-ischemic brain injury. In this study, we investigated the relationship between alpha(v)beta(8) and TGF-beta1 activation, and thus the effects of TGF-beta1 activation in the protection of neurons after hypoxia-ischemia (HI). Astrocytes and neurons from rat brains were cultured and then subjected to oxygen-glucose deprivation to generate HI model in vitro. beta(8) expression was determined using immunocytochemistry, western blot, and reverse-transcriptase polymerase chain reaction. TGF-beta1 activation was determined by TGF-beta bioassay in a tested cell (astrocyte) and a reporter cell co-culture system. The pro-apoptotic protein, cleaved caspase-3, and the anti-apoptotic protein, Bcl-2 and Bcl-xL, were detected using western blot. Cellular apoptosis was detected with TUNEL. We found that beta(8) expression was stronger in astrocytes than that in neurons under normoxia. HI resulted in a rapid and persistent increase of beta(8) expression in astrocytes, but only in a slight and transient increase in neurons. Astrocytes beta(8) could induce TGF-beta1 leading to upregulation of Bcl-2 and Bcl-xL, and thus attenuated neuronal apoptosis. The present findings suggest that beta(8) protecting the brain against neonatal HI injury through TGF-beta1 signaling pathway, which may have implications for the treatment of HI brain injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Animals, Newborn
  • Apoptosis / physiology
  • Astrocytes
  • Brain / cytology
  • Cells, Cultured
  • Coculture Techniques / methods
  • Gene Expression / physiology
  • Glucose / deficiency*
  • Hypoxia / pathology*
  • In Situ Nick-End Labeling
  • Neurons / drug effects
  • Neurons / metabolism*
  • Oxygen / pharmacology
  • Proto-Oncogene Proteins / metabolism
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction / drug effects
  • Statistics, Nonparametric
  • Time Factors
  • Trans-Activators / metabolism
  • Transfection / methods
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / metabolism*
  • bcl-X Protein / metabolism

Substances

  • Bcl2l1 protein, rat
  • MYBL1 protein, human
  • Proto-Oncogene Proteins
  • RNA, Messenger
  • RNA, Small Interfering
  • Trans-Activators
  • Transforming Growth Factor beta
  • bcl-X Protein
  • Glucose
  • Oxygen