Expression of Activating Transcription Factor 3 in Ischemic Penumbra Region Following Focal Cerebral Ischemia.
- Author:
Dae Yong SONG
1
;
Kyoung Min OH
;
Ji Hye LEE
;
Ran Sook WOO
;
Yun Jeong LEE
;
Jung Tae HAN
;
Tai Kyoung BAIK
Author Information
1. Department of Anatomy and Neurosciences, School of Medicine and Medical Sciences Research Institute, Eulji University, Daejeon, Korea. tkbaik@eulji.ac.kr
- Publication Type:Original Article
- Keywords:
Activating transcription factor 3;
Cerebral ischemia;
Immediate-early gene
- MeSH:
Activating Transcription Factor 3;
Astrocytes;
Brain;
Brain Injuries;
Brain Ischemia;
Cell Death;
Coloring Agents;
Eosinophils;
Genes, Immediate-Early;
Humans;
Microglia;
Middle Cerebral Artery;
Necrosis;
Neurons;
Research Personnel;
Tetrazolium Salts;
Up-Regulation
- From:Korean Journal of Anatomy
2008;41(3):173-183
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
It has been demonstrated that some of immediate early genes (IEGs) such as c-Jun or fos are induced immediately following neuronal injury and they play an important role in determining the fate of the injured neurons. Of IEGs, the activating transcription factor 3 (ATF3) is focused by many investigators, because they are expressed in various types of neural insults and have been known to serve a diverse function in both neuronal survival and death. However, little is known about the functional role of ATF3 in ischemic brain injury. So in this study, the authors examined the expression pattern of the activating transcription factor 3 (ATF3) following middle cerebral artery (MCA) occlusion-reperfusion injury. According to the findings obtained by triphenyltetrazolium chloride (TTC) stains, the authors have classified the infarcted area into two regions, the ischemic core region and the ischemic penumbra region. In both regions, many neurons underwent neuronal degeneration, characterized by the shrunken nuclei with eosinophilic perikaryon. The H & E stain also demonstrated the increased number of probable activated astrocytes and microglia in the ischemic brain regions and this was confirmed by GFAP- and OX42-immunohistochemistry. Immunohistochemical study for ATF3 also demonstrated the specific upregulation of ATF3 in the nuclei of neurons under ischemic injury, but not in those of the contralateral regions. Interestingly, the number of the ATF3 positive neurons in the ischemic penumbra regions outnumbered that of the ischemic core regions. Based on many reports that the neuronal death in ischemic penumbra region is caused by programed cell death rather than by necrosis which is main cause of neuronal death in ischemic core region, our results could suggest that the ATF3 is an important IEGs which determine the fate of the ischemic neurons.
