Effect of endoplasmic reticulum stress in VEGF-induced neuroprotection

J Invest Surg. 2009 Jan-Feb;22(1):29-34. doi: 10.1080/08941930802566714.

Abstract

Researchers suggest that endoplasmic reticulum (ER) stress cause apoptosis after ischemia. Caspase-12 has been localized to the ER and is a signal for apoptosis. We sought to clarify the role of caspase-12 in the vascular endothelial growth factor (VEGF) induced neuroprotective effect. Transient focal cerebral ischemia was produced by occluding left middle cerebral artery in rabbit. The expressions of caspase-12 and caspase-3 were detected by immunohistochemistry. Neuronal apoptosis was detected by TUNEL staining. We confirmed that the number of apoptotic cells and the expressions of caspase-12 and caspase-3 significantly increased during reperfusion. VEGF inhibited the cell apoptosis and the expressions of caspase-12 and caspase-3. These results suggest that VEGF may protect neurons from apoptosis by inhibiting ER stress pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis*
  • Caspase 12 / metabolism*
  • Caspase 3 / metabolism
  • Cerebrum / pathology
  • Endoplasmic Reticulum / metabolism*
  • Flow Cytometry
  • In Situ Nick-End Labeling
  • Infarction, Middle Cerebral Artery / metabolism*
  • Infarction, Middle Cerebral Artery / pathology
  • Male
  • Rabbits
  • Reperfusion
  • Reperfusion Injury / pathology
  • Stress, Physiological
  • Vascular Endothelial Growth Factor A / metabolism*

Substances

  • Vascular Endothelial Growth Factor A
  • Caspase 12
  • Caspase 3