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Age-dependent differences in myelin basic protein expression in the hippocampus of young, adult and aged gerbils
Myelin degeneration is one of the characteristics of aging and degenerative diseases. This study investigated age-related alterations in expression of myelin basic protein (MBP) in the hippocampal subregions (dentate gyrus, CA2/3 and CA1 areas) of gerbils of various ages; young (1 month), adult (6 m...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Association for Laboratory Animal Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645602/ https://www.ncbi.nlm.nih.gov/pubmed/29046699 http://dx.doi.org/10.5625/lar.2017.33.3.237 |
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author | Ahn, Ji Hyeon Lee, Tae-Kyeong Park, Joon Ha Cho, Jeong Hwi Kim, In Hye Lee, Jae Chul Hong, Seongkweon Jeon, Yong Hwan Kang, Il Jun Lee, Young Joo Won, Moo-Ho Lee, Choong-Hyun |
author_facet | Ahn, Ji Hyeon Lee, Tae-Kyeong Park, Joon Ha Cho, Jeong Hwi Kim, In Hye Lee, Jae Chul Hong, Seongkweon Jeon, Yong Hwan Kang, Il Jun Lee, Young Joo Won, Moo-Ho Lee, Choong-Hyun |
author_sort | Ahn, Ji Hyeon |
collection | PubMed |
description | Myelin degeneration is one of the characteristics of aging and degenerative diseases. This study investigated age-related alterations in expression of myelin basic protein (MBP) in the hippocampal subregions (dentate gyrus, CA2/3 and CA1 areas) of gerbils of various ages; young (1 month), adult (6 months) and aged (24 months), using western blot and immunohistochemistry. Western blot results showed tendencies of age-related reductions of MBP levels. MBP immunoreactivity was significantly decreased with age in synaptic sites of trisynaptic loops, perforant paths, mossy fibers, and Schaffer collaterals. In particular, MBP immunoreactive fibers in the dentate molecular cell layer (perforant path) was significantly reduced in adult and aged subjects. In addition, MBP immunoreactive mossy fibers in the dentate polymorphic layer and in the CA3 striatum radiatum was significantly decreased in the aged group. Furthermore, we observed similar age-related alterations in the CA1 stratum radiatum (Schaffer collaterals). However, the density of MBP immunoreactive fibers in the dentate granular cell layer and CA stratum pyramidale was decreased with aging. These findings indicate that expression of MBP is age-dependent and tissue specific according to hippocampal layers. |
format | Online Article Text |
id | pubmed-5645602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Korean Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56456022017-10-18 Age-dependent differences in myelin basic protein expression in the hippocampus of young, adult and aged gerbils Ahn, Ji Hyeon Lee, Tae-Kyeong Park, Joon Ha Cho, Jeong Hwi Kim, In Hye Lee, Jae Chul Hong, Seongkweon Jeon, Yong Hwan Kang, Il Jun Lee, Young Joo Won, Moo-Ho Lee, Choong-Hyun Lab Anim Res Original Article Myelin degeneration is one of the characteristics of aging and degenerative diseases. This study investigated age-related alterations in expression of myelin basic protein (MBP) in the hippocampal subregions (dentate gyrus, CA2/3 and CA1 areas) of gerbils of various ages; young (1 month), adult (6 months) and aged (24 months), using western blot and immunohistochemistry. Western blot results showed tendencies of age-related reductions of MBP levels. MBP immunoreactivity was significantly decreased with age in synaptic sites of trisynaptic loops, perforant paths, mossy fibers, and Schaffer collaterals. In particular, MBP immunoreactive fibers in the dentate molecular cell layer (perforant path) was significantly reduced in adult and aged subjects. In addition, MBP immunoreactive mossy fibers in the dentate polymorphic layer and in the CA3 striatum radiatum was significantly decreased in the aged group. Furthermore, we observed similar age-related alterations in the CA1 stratum radiatum (Schaffer collaterals). However, the density of MBP immunoreactive fibers in the dentate granular cell layer and CA stratum pyramidale was decreased with aging. These findings indicate that expression of MBP is age-dependent and tissue specific according to hippocampal layers. Korean Association for Laboratory Animal Science 2017-09 2017-09-27 /pmc/articles/PMC5645602/ /pubmed/29046699 http://dx.doi.org/10.5625/lar.2017.33.3.237 Text en Copyright © 2017 Korean Association for Laboratory Animal Science http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Ahn, Ji Hyeon Lee, Tae-Kyeong Park, Joon Ha Cho, Jeong Hwi Kim, In Hye Lee, Jae Chul Hong, Seongkweon Jeon, Yong Hwan Kang, Il Jun Lee, Young Joo Won, Moo-Ho Lee, Choong-Hyun Age-dependent differences in myelin basic protein expression in the hippocampus of young, adult and aged gerbils |
title | Age-dependent differences in myelin basic protein expression in the hippocampus of young, adult and aged gerbils |
title_full | Age-dependent differences in myelin basic protein expression in the hippocampus of young, adult and aged gerbils |
title_fullStr | Age-dependent differences in myelin basic protein expression in the hippocampus of young, adult and aged gerbils |
title_full_unstemmed | Age-dependent differences in myelin basic protein expression in the hippocampus of young, adult and aged gerbils |
title_short | Age-dependent differences in myelin basic protein expression in the hippocampus of young, adult and aged gerbils |
title_sort | age-dependent differences in myelin basic protein expression in the hippocampus of young, adult and aged gerbils |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645602/ https://www.ncbi.nlm.nih.gov/pubmed/29046699 http://dx.doi.org/10.5625/lar.2017.33.3.237 |
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