Abstract
In the present study, we examined patterns of A-myb expression in the kainic acid (KA)-treated mouse hippocampus. Western blot analysis revealed that A-myb expression was dramatically increased in brain 3 days after KA treatment, and was sustained for more than 7 days. A-myb immunoreactivity was restricted to hippocampal neurons in control mice. Three days after KA treatment, strong A-myb immunoreactivity was observed in reactive astrocytes throughout the CA3 region. Thereafter, A-myb immunoreactive astrocytes gradually concentrated around the CA3 region in parallel with selective neuronal loss, and only a few A-myb immunoreactive astrocytes persisted in the CA3 region 14 days after KA treatment. These findings suggest that the A-myb plays a role in the reactive gliosis signaling pathway in KA-induced excitotoxic lesions.
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This study was supported by grant no 21-2004-037 from the Seoul National University Hospital Research Fund, and in part by year 2006 the Second stage of BK 21 Project.
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Jeon, G.S., Byun, H.J., Park, S.K. et al. Induction of Transcription Factor A-myb Expression in Reactive Astrocytes Following an Excitotoxic Lesion in the Mouse Hippocampus. Neurochem Res 31, 1371–1374 (2006). https://doi.org/10.1007/s11064-006-9184-x
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DOI: https://doi.org/10.1007/s11064-006-9184-x