Immunohistochemical study on the distribution of phosphorylated extracellular signal-regulated kinase (ERK) in the central nervous system of SOD1G93A transgenic mice

被引:32
作者
Chung, YH
Joo, KM
Lim, HC
Cho, MH
Kim, D
Lee, WB
Cha, CI
机构
[1] Seoul Natl Univ, Coll Med, Dept Anat, Seoul 110799, South Korea
[2] Chung Ang Univ, Coll Med, Dept Anat, Seoul 156756, South Korea
[3] Seoul Natl Univ, Med Ctr, Neurosci Res Inst, Seoul 110799, South Korea
[4] KNIH, Biomed Brain Res Ctr, Seoul, South Korea
关键词
amyotrophic lateral sclerosis (ALS); extracellular signal-regulated kinases (ERK); SOD1(G93A) mutant transgenic mice; astrocyte;
D O I
10.1016/j.brainres.2005.05.060
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
In the present study, we performed immunohistochemical studies to investigate the changes of phosphorylated extracellular signal-regulated kinases (PERK) in the central nervous system of SOD1(G93A) transgenic mice. In symptomatic transgenic mice, pERK-immunoreactive astrocytes were detected in the spinal cord, brainstem, central gray and cerebellar nuclei. In contrast to symptomatic mice, no pERK-immunoreactive astrocytes were observed in any brain region of wtSOD1 and presymptomatic mice, and the number and intensity of stained neurons were not different at the age of 8 weeks and 13 weeks. Interestingly, region-specific alterations in pERK immunoreactivity were observed in the hippocampal region and cerebellum. These results provide the first evidence that pERK-immunoreactive astrocytes were found in the CNS of SOD1(G93A) transgenic mice after clinical symptoms, showing a possible consequence of the pathological process of ALS. This study has also demonstrated that pERK increases in the hippocampus and cerebellum, suggesting a role of pERK in an abnormality of cognitive and/or motor function in ALS, respectively. However, the mechanisms underlying the increased immunoreactivity for pERK and the functional implications require elucidation. (C) 2005 Elsevier B.V All rights reserved.
引用
收藏
页码:203 / 209
页数:7
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