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Strain‐specific differential expression of astrocytes and microglia in the mouse hippocampus
INTRODUCTION: Genetic background influences neurotransmitter expression and function of the hippocampus. Genetic background influences the phenotype of the hippocampus, but expression of neuroglia in hippocampus has not been well established dependent on various mouse strains. OBJECTIVES: In this st...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943717/ https://www.ncbi.nlm.nih.gov/pubmed/29761014 http://dx.doi.org/10.1002/brb3.961 |
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author | Kim, Jong Whi Nam, Sung Min Yoo, Dae Young Jung, Hyo Young Hwang, In Koo Seong, Je Kyung Yoon, Yeo Sung |
author_facet | Kim, Jong Whi Nam, Sung Min Yoo, Dae Young Jung, Hyo Young Hwang, In Koo Seong, Je Kyung Yoon, Yeo Sung |
author_sort | Kim, Jong Whi |
collection | PubMed |
description | INTRODUCTION: Genetic background influences neurotransmitter expression and function of the hippocampus. Genetic background influences the phenotype of the hippocampus, but expression of neuroglia in hippocampus has not been well established dependent on various mouse strains. OBJECTIVES: In this study, we investigated the effects of genetic background on cell population of astrocytes and microglia in eight widely used inbred strains (C57BL/6J, A/J, BALB/c, C3H/HeJ, FVB, 129/SvJ, DBA/1, and DBA/2) and one outbred strain (ICR). METHODS: In all mouse strains, glial fibrillary acidic protein (GFAP)‐immunoreactive astrocytes and ionized calcium‐binding adaptor molecule 1 (Iba‐1)‐immunoreactive microglia were found in almost all layers of hippocampal CA1‐4 regions and the dentate gyrus. RESULTS: We observed significant differences in the number of astrocytes and microglia. In the CA1 and CA3 regions, the number of GFAP‐immunoreactive astrocytes was highest in the C3H/HeJ strain, and lowest in the 129/SvJ and FVB strains. In the polymorphic layer of the dentate gyrus, the number was highest in the DBA/1 strain and lowest in the 129/SvJ strain. Among the nine mouse strains, the number of Iba‐1‐immunoreactive microglia was highest in the CA1 and CA3 regions in the ICR and in the dentate gyrus of the C57BL/6 strain. The CA1 region of the FVB strain and the CA3 region and dentate gyrus of DBA/2 had the lowest number of Iba‐1‐immunoreactive microglia. CONCLUSION: These results suggest that the numbers of astrocytes and microglia differ depending on the mouse strain and these differences may be related to strain‐dependent function of astrocytes. |
format | Online Article Text |
id | pubmed-5943717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59437172018-05-14 Strain‐specific differential expression of astrocytes and microglia in the mouse hippocampus Kim, Jong Whi Nam, Sung Min Yoo, Dae Young Jung, Hyo Young Hwang, In Koo Seong, Je Kyung Yoon, Yeo Sung Brain Behav Original Research INTRODUCTION: Genetic background influences neurotransmitter expression and function of the hippocampus. Genetic background influences the phenotype of the hippocampus, but expression of neuroglia in hippocampus has not been well established dependent on various mouse strains. OBJECTIVES: In this study, we investigated the effects of genetic background on cell population of astrocytes and microglia in eight widely used inbred strains (C57BL/6J, A/J, BALB/c, C3H/HeJ, FVB, 129/SvJ, DBA/1, and DBA/2) and one outbred strain (ICR). METHODS: In all mouse strains, glial fibrillary acidic protein (GFAP)‐immunoreactive astrocytes and ionized calcium‐binding adaptor molecule 1 (Iba‐1)‐immunoreactive microglia were found in almost all layers of hippocampal CA1‐4 regions and the dentate gyrus. RESULTS: We observed significant differences in the number of astrocytes and microglia. In the CA1 and CA3 regions, the number of GFAP‐immunoreactive astrocytes was highest in the C3H/HeJ strain, and lowest in the 129/SvJ and FVB strains. In the polymorphic layer of the dentate gyrus, the number was highest in the DBA/1 strain and lowest in the 129/SvJ strain. Among the nine mouse strains, the number of Iba‐1‐immunoreactive microglia was highest in the CA1 and CA3 regions in the ICR and in the dentate gyrus of the C57BL/6 strain. The CA1 region of the FVB strain and the CA3 region and dentate gyrus of DBA/2 had the lowest number of Iba‐1‐immunoreactive microglia. CONCLUSION: These results suggest that the numbers of astrocytes and microglia differ depending on the mouse strain and these differences may be related to strain‐dependent function of astrocytes. John Wiley and Sons Inc. 2018-03-22 /pmc/articles/PMC5943717/ /pubmed/29761014 http://dx.doi.org/10.1002/brb3.961 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Kim, Jong Whi Nam, Sung Min Yoo, Dae Young Jung, Hyo Young Hwang, In Koo Seong, Je Kyung Yoon, Yeo Sung Strain‐specific differential expression of astrocytes and microglia in the mouse hippocampus |
title | Strain‐specific differential expression of astrocytes and microglia in the mouse hippocampus |
title_full | Strain‐specific differential expression of astrocytes and microglia in the mouse hippocampus |
title_fullStr | Strain‐specific differential expression of astrocytes and microglia in the mouse hippocampus |
title_full_unstemmed | Strain‐specific differential expression of astrocytes and microglia in the mouse hippocampus |
title_short | Strain‐specific differential expression of astrocytes and microglia in the mouse hippocampus |
title_sort | strain‐specific differential expression of astrocytes and microglia in the mouse hippocampus |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943717/ https://www.ncbi.nlm.nih.gov/pubmed/29761014 http://dx.doi.org/10.1002/brb3.961 |
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