TY - JOUR
T1 - Induction of phosphorylated-Stat3 following focal cerebral ischemia in mice
AU - Wen, Tong Chun
AU - Peng, Hui
AU - Hata, Ryuji
AU - Desaki, Junzo
AU - Sakanaka, Masahiro
N1 - Funding Information:
This study was supported in part by Grants-in-aid for scientific research from the Ministry of Education, Science, Sports and Culture in Japan. The authors are grateful to Dr Kazumasa Ikoma for his encouragement and fruitful suggestions throughout this work.
PY - 2001/5/11
Y1 - 2001/5/11
N2 - It has been shown that Stat3 is induced following transient cerebral ischemia in rat. However there is no evidence that cerebral ischemia stimulates the expression of phosphorylated-Stat3 (p-Stat3), which can activate cytokine-mediated signal transduction from the membrane to the nucleus. In the present study, we investigated the changes in p-Stat3 expression following middle cerebral artery occlusion in mice. Western blot analysis revealed a significant increase in the p-Stat3 protein in the peripheral part of the ischemic area, starting from 6 h after ischemia. p-Stat3 immunoreactivity was detected only in neurons, but not in astrocytes or microglia, and p-Stat3-positive neurons were increased in number in the peripheral part of the ischemic area at 24 h after ischemia. Double staining with aTdT-mediated biotinylated UTP nick end labeling (TUNEL) kit and the p-Stat3 antibody indicated that p-Stat3-positive neurons were also TUNEL-positive. Subsequent immuno-electron microscopic observations showed that p-Stat3-positive neurons were at different stages of degeneration. The present findings suggest that the increased expression of p-Stat3 after cerebral ischemia could play a crucial role in ischemia-induced neuron death.
AB - It has been shown that Stat3 is induced following transient cerebral ischemia in rat. However there is no evidence that cerebral ischemia stimulates the expression of phosphorylated-Stat3 (p-Stat3), which can activate cytokine-mediated signal transduction from the membrane to the nucleus. In the present study, we investigated the changes in p-Stat3 expression following middle cerebral artery occlusion in mice. Western blot analysis revealed a significant increase in the p-Stat3 protein in the peripheral part of the ischemic area, starting from 6 h after ischemia. p-Stat3 immunoreactivity was detected only in neurons, but not in astrocytes or microglia, and p-Stat3-positive neurons were increased in number in the peripheral part of the ischemic area at 24 h after ischemia. Double staining with aTdT-mediated biotinylated UTP nick end labeling (TUNEL) kit and the p-Stat3 antibody indicated that p-Stat3-positive neurons were also TUNEL-positive. Subsequent immuno-electron microscopic observations showed that p-Stat3-positive neurons were at different stages of degeneration. The present findings suggest that the increased expression of p-Stat3 after cerebral ischemia could play a crucial role in ischemia-induced neuron death.
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U2 - 10.1016/S0304-3940(01)01711-6
DO - 10.1016/S0304-3940(01)01711-6
M3 - Article
C2 - 11323108
AN - SCOPUS:0035843971
SN - 0304-3940
VL - 303
SP - 153
EP - 156
JO - Neuroscience Letters
JF - Neuroscience Letters
IS - 3
ER -