Phosphorylated extracellular signal-regulated kinase 1/2 immunoreactivity and its protein levels in the gerbil hippocampus during normal aging
Phosphorylated extracellular signal-regulated kinase (pERK) mediates neuronal synaptic plasticity, long-term potentiation, and learning and memory in the hippocampus. In this study, we examined pERK1/2 immunoreactivity and its protein level in the gerbil hippocampus at various ages. In the postnatal...
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Published in | Molecules and cells Vol. 29; no. 4; pp. 373 - 378 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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Springer
Korean Society for Molecular and Cellular Biology
01.04.2010
한국분자세포생물학회 |
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ISSN | 1016-8478 0219-1032 |
DOI | 10.1007/s10059-010-0046-7 |
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Abstract | Phosphorylated extracellular signal-regulated kinase (pERK) mediates neuronal synaptic plasticity, long-term potentiation, and learning and memory in the hippocampus. In this study, we examined pERK1/2 immunoreactivity and its protein level in the gerbil hippocampus at various ages. In the postnatal month 1 (PM 1) group, very weak pERK1/2 immunoreactivity was detected in the hippocampus. In the CA1 region, pERK1/2 immunoreactivity was considerably increased in the stratum pyramidale in the PM 6 group. Thereafter, pERK1/2 immunoreactivity was decreased. In the CA2/3 region, pERK1/2 immunoreactivity increased in an age-dependent manner until PM 12. Thereafter, numbers of pERK1/2-immunoreactive neurons were decreased. However, in the mossy fiber zone, pERK1/2 immunostaining became stronger with age. In the dentate gyrus, a few pERK1/2-immunoreactive cells were observed until PM 12. In the PM 18 and 24 groups, numbers of pERK1/2-immunoreactive cells were increased, especially in the polymorphic layer. In Western blot analysis, pERK1/2 level in the gerbil hippocampus was increased with age. These results indicate that total pERK1/2 levels are increased in the hippocampus with age. However pERK1/2 immunoreactivity in subregions of the gerbil hippocampus was changed with different pattern during normal aging. |
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AbstractList | Phosphorylated extracellular signal-regulated kinase (pERK) mediates neuronal synaptic plasticity, long-term potentiation, and learning and memory in the hippocampus. In this study, we examined pERK1/2 immunoreactivity and its protein level in the gerbil hippocampus at various ages. In the postnatal month 1 (PM 1) group, very weak pERK1/2 immunoreactivity was detected in the hippocampus. In the CA1 region, pERK1/2 immunoreactivity was considerably increased in the stratum pyramidale in the PM 6 group. Thereafter, pERK1/2 immunoreactivity was decreased. In the CA2/3 region, pERK1/2 immunoreactivity increased in an age-dependent manner until PM 12. Thereafter, numbers of pERK1/2-immunoreactive neurons were decreased. However, in the mossy fiber zone, pERK1/2 immunostaining became stronger with age. In the dentate gyrus, a few pERK1/2-immunoreactive cells were observed until PM 12. In the PM 18 and 24 groups, numbers of pERK1/2-immunoreactive cells were increased, especially in the polymorphic layer. In Western blot analysis, pERK1/2 level in the gerbil hippocampus was increased with age. These results indicate that total pERK1/2 levels are increased in the hippocampus with age. However pERK1/2 immunoreactivity in subregions of the gerbil hippocampus was changed with different pattern during normal aging. Phosphorylated extracellular signal-regulated kinase (pERK) mediates neuronal synaptic plasticity, long-term potentiation, and learning and memory in the hippocampus. In this study, we examined pERK1/2 immunoreactivity and its protein level in the gerbil hippocampus at various ages. In the postnatal month 1 (PM 1) group, very weak pERK1/2 immunoreactivity was detected in the hippocampus. In the CA1 region, pERK1/2 immunoreactivity was considerably increased in the stratum pyramidale in the PM 6 group. Thereafter, pERK1/2 immunoreactivity was decreased. In the CA2/3 region, pERK1/2 immunoreactivity increased in an age-dependent manner until PM 12. Thereafter, numbers of pERK1/2-immunoreactive neurons were decreased. However, in the mossy fiber zone, pERK1/2 immunostaining became stronger with age. In the dentate gyrus, a few pERK1/2-immunoreactive cells were observed until PM 12. In the PM 18 and 24 groups, numbers of pERK1/2-immunoreactive cells were increased, especially in the polymorphic layer. In Western blot analysis, pERK1/2 level in the gerbil hippocampus was increased with age. These results indicate that total pERK1/2 levels are increased in the hippocampus with age. However pERK1/2 immunoreactivity in subregions of the gerbil hippocampus was changed with different pattern during normal aging.[PUBLICATION ABSTRACT] Phosphorylated extracellular signal-regulated kinase (pERK) mediates neuronal synaptic plasticity, long-term potentia-tion, and learning and memory in the hippocampus. In this study, we examined pERK1/2 immunoreactivity and its protein level in the gerbil hippocampus at various ages. In the postnatal month 1 (PM 1) group, very weak pERK1/2 immunoreactivity was detected in the hippocampus. In the CA1 region, pERK1/2 immunoreactivity was considerably increased in the stratum pyramidale in the PM 6 group. Thereafter, pERK1/2 immunoreactivity was decreased. In the CA2/3 region, pERK1/2 immunoreactivity increased in an age-dependent manner until PM 12. Thereafter, num-bers of pERK1/2-immunoreactive neurons were decreased. However, in the mossy fiber zone, pERK1/2 immunostain-ing became stronger with age. In the dentate gyrus, a few pERK1/2-immunoreactive cells were observed until PM 12. In the PM 18 and 24 groups, numbers of pERK1/2-immunoreactive cells were increased, especially in the polymorphic layer. In Western blot analysis, pERK1/2 level in the gerbil hippocampus was increased with age. These results indicate that total pERK1/2 levels are increased in the hippocampus with age. However pERK1/2 immunore-activity in subregions of the gerbil hippocampus was changed with different pattern during normal aging. KCI Citation Count: 9 |
Author | Kim, S.K., Kangnam Sacred Heart Hospital, College of Medicine, Hallym University, Seoul, Republic of Korea Hwang, I.K., Seoul National University, Seoul, Republic of Korea Choi, J.H., Hallym University, Chuncheon, Republic of Korea Won, M.H., Hallym University, Chuncheon, Republic of Korea Bae, E.J., Hallym University, Chuncheon, Republic of Korea Lee, C.H., Hallym University, Chuncheon, Republic of Korea Yoo, K.Y., Hallym University, Chuncheon, Republic of Korea Park, O.K., Hallym University, Chuncheon, Republic of Korea Kang, I.J., Hallym University, Chuncheon, Republic of Korea |
Author_xml | – sequence: 1 fullname: Lee, C.H., Hallym University, Chuncheon, Republic of Korea – sequence: 2 fullname: Yoo, K.Y., Hallym University, Chuncheon, Republic of Korea – sequence: 3 fullname: Park, O.K., Hallym University, Chuncheon, Republic of Korea – sequence: 4 fullname: Choi, J.H., Hallym University, Chuncheon, Republic of Korea – sequence: 5 fullname: Kang, I.J., Hallym University, Chuncheon, Republic of Korea – sequence: 6 fullname: Bae, E.J., Hallym University, Chuncheon, Republic of Korea – sequence: 7 fullname: Kim, S.K., Kangnam Sacred Heart Hospital, College of Medicine, Hallym University, Seoul, Republic of Korea – sequence: 8 fullname: Hwang, I.K., Seoul National University, Seoul, Republic of Korea – sequence: 9 fullname: Won, M.H., Hallym University, Chuncheon, Republic of Korea |
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CitedBy_id | crossref_primary_10_1159_000439026 crossref_primary_10_1111_j_1439_0264_2011_01083_x crossref_primary_10_2174_1567202616666190618114250 crossref_primary_10_1007_s11064_012_0752_y crossref_primary_10_1155_2015_414965 crossref_primary_10_3390_ijms222011223 crossref_primary_10_1007_s10571_010_9638_1 |
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