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Amyloid Beta(1-40)-Induced Astrogliosis and the Effect of Genistein Treatment in Rat: A Three-Dimensional Confocal Morphometric and Proteomic Study
Astrocytes are highly involved in regulation and homeostasis of the extracellular environment in the healthy brain. In pathological conditions, these cells play a major role in the inflammatory response seen in CNS tissues, which is called reactive astrogliosis and includes hypertrophy and prolifera...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793933/ https://www.ncbi.nlm.nih.gov/pubmed/24130779 http://dx.doi.org/10.1371/journal.pone.0076526 |
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author | Bagheri, Maryam Rezakhani, Arjang Nyström, Sofie Turkina, Maria V. Roghani, Mehrdad Hammarström, Per Mohseni, Simin |
author_facet | Bagheri, Maryam Rezakhani, Arjang Nyström, Sofie Turkina, Maria V. Roghani, Mehrdad Hammarström, Per Mohseni, Simin |
author_sort | Bagheri, Maryam |
collection | PubMed |
description | Astrocytes are highly involved in regulation and homeostasis of the extracellular environment in the healthy brain. In pathological conditions, these cells play a major role in the inflammatory response seen in CNS tissues, which is called reactive astrogliosis and includes hypertrophy and proliferation of astrocytes. Here, we performed 3D confocal microscopy to evaluate the morphological response of reactive astrocytes positive for glial fibrillary acidic protein (GFAP) in rats, to the presence of Aβ(1–40) in the rat brain before and after treatment with genistein. In 50 astrocytes per animal, we measured the volume and surface area for the nucleus, cell body, the entire cell, the tissue covered by single astrocytes and quantified the number and length of branches, the density of the astrocytes and the intensity of GFAP immunoreactivity. Injecting Aβ(1–40) into the brain of rats caused astrogliosis indicated by increased values for all measured parameters. Mass spectrometric analysis of hippocampal tissue in Aβ(1–40)-injected brain showed decreased amounts of tubulins, enolases and myelin basic protein, and increased amounts of dihydropyrimidinase-related protein 2. In Aβ(1–40)-injected rats pretreated with genistein, GFAP intensity was decreased to the sham-operated group level, and Aβ(1–40)-induced astrogliosis was significantly ameliorated. |
format | Online Article Text |
id | pubmed-3793933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37939332013-10-15 Amyloid Beta(1-40)-Induced Astrogliosis and the Effect of Genistein Treatment in Rat: A Three-Dimensional Confocal Morphometric and Proteomic Study Bagheri, Maryam Rezakhani, Arjang Nyström, Sofie Turkina, Maria V. Roghani, Mehrdad Hammarström, Per Mohseni, Simin PLoS One Research Article Astrocytes are highly involved in regulation and homeostasis of the extracellular environment in the healthy brain. In pathological conditions, these cells play a major role in the inflammatory response seen in CNS tissues, which is called reactive astrogliosis and includes hypertrophy and proliferation of astrocytes. Here, we performed 3D confocal microscopy to evaluate the morphological response of reactive astrocytes positive for glial fibrillary acidic protein (GFAP) in rats, to the presence of Aβ(1–40) in the rat brain before and after treatment with genistein. In 50 astrocytes per animal, we measured the volume and surface area for the nucleus, cell body, the entire cell, the tissue covered by single astrocytes and quantified the number and length of branches, the density of the astrocytes and the intensity of GFAP immunoreactivity. Injecting Aβ(1–40) into the brain of rats caused astrogliosis indicated by increased values for all measured parameters. Mass spectrometric analysis of hippocampal tissue in Aβ(1–40)-injected brain showed decreased amounts of tubulins, enolases and myelin basic protein, and increased amounts of dihydropyrimidinase-related protein 2. In Aβ(1–40)-injected rats pretreated with genistein, GFAP intensity was decreased to the sham-operated group level, and Aβ(1–40)-induced astrogliosis was significantly ameliorated. Public Library of Science 2013-10-09 /pmc/articles/PMC3793933/ /pubmed/24130779 http://dx.doi.org/10.1371/journal.pone.0076526 Text en © 2013 Bagheri et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Bagheri, Maryam Rezakhani, Arjang Nyström, Sofie Turkina, Maria V. Roghani, Mehrdad Hammarström, Per Mohseni, Simin Amyloid Beta(1-40)-Induced Astrogliosis and the Effect of Genistein Treatment in Rat: A Three-Dimensional Confocal Morphometric and Proteomic Study |
title | Amyloid Beta(1-40)-Induced Astrogliosis and the Effect of Genistein Treatment in Rat: A Three-Dimensional Confocal Morphometric and Proteomic Study |
title_full | Amyloid Beta(1-40)-Induced Astrogliosis and the Effect of Genistein Treatment in Rat: A Three-Dimensional Confocal Morphometric and Proteomic Study |
title_fullStr | Amyloid Beta(1-40)-Induced Astrogliosis and the Effect of Genistein Treatment in Rat: A Three-Dimensional Confocal Morphometric and Proteomic Study |
title_full_unstemmed | Amyloid Beta(1-40)-Induced Astrogliosis and the Effect of Genistein Treatment in Rat: A Three-Dimensional Confocal Morphometric and Proteomic Study |
title_short | Amyloid Beta(1-40)-Induced Astrogliosis and the Effect of Genistein Treatment in Rat: A Three-Dimensional Confocal Morphometric and Proteomic Study |
title_sort | amyloid beta(1-40)-induced astrogliosis and the effect of genistein treatment in rat: a three-dimensional confocal morphometric and proteomic study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793933/ https://www.ncbi.nlm.nih.gov/pubmed/24130779 http://dx.doi.org/10.1371/journal.pone.0076526 |
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