Characterization of nestin expression in astrocytes in the rat hippocampal CA1 region following transient forebrain ischemia.
10.5115/acb.2013.46.2.131
- Author:
Jeong Min CHO
1
;
Yoo Jin SHIN
;
Jang Mi PARK
;
Jin KIM
;
Mun Yong LEE
Author Information
1. Department of Anatomy and Cell Death Disease Research Center, The Catholic University of Korea College of Medicine, Seoul, Korea. munylee@catholic.ac.kr
- Publication Type:Original Article
- Keywords:
Nestin;
Transient forebrain ischemia;
Reactive astrocytes;
Hippocampus
- MeSH:
Animals;
Astrocytes;
CA1 Region, Hippocampal;
Hippocampus;
Intermediate Filament Proteins;
Ischemia;
Nerve Tissue Proteins;
Neurons;
Prosencephalon;
Pyramidal Cells;
Rats;
Transcription Factors
- From:Anatomy & Cell Biology
2013;46(2):131-140
- CountryRepublic of Korea
- Language:English
-
Abstract:
Recent studies have suggested that nestin facilitates cellular structural remodeling in vasculature-associated cells in response to ischemic injury. The current study was designed to investigate the potential role of post-ischemic nestin expression in parenchymal astrocytes. With this aim, we characterized ischemia-induced nestin expression in the CA1 hippocampal region, an area that undergoes a delayed neuronal death, followed by a lack of neuronal generation after transient forebrain ischemia. Virtually all of the nestin-positive cells in the ischemic CA1 hippocampus were reactive astrocytes. However, induction of nestin expression did not correlate simply with astrogliosis, but rather showed characteristic time- and strata-dependent expression patterns. Nestin induction in astrocytes of the pyramidal cell layer was rapid and transient, while a long-lasting induction of nestin was observed in astrocytes located in the CA1 dendritic subfields, such as the stratum oriens and radiatum, until at least day 28 after ischemia. There was no detectable expression in the stratum lacunosum moleculare despite the evident astroglial reaction. Almost all of the nestin-positive cells also expressed a transcription factor for neural/glial progenitors, i.e., Sox-2 or Sox-9, and some cells were also positive for Ki-67. However, all of the nestin-positive astrocytes expressed the calcium-binding protein S100beta, which is known to be expressed in a distinct, post-mitotic astrocyte population. Thus, our data indicate that in the ischemic CA1 hippocampus, nestin expression was induced in astroglia that were becoming reactive, but not in a progenitor/stem cell population, suggesting that nestin may allow for the structural remodeling of these cells in response to ischemic injury.
