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Microglial cell response to neuronal degeneration in the brain of brindled mouse
Reactive changes of microglia in response to neuronal degeneration were investigated in the brains of brindled mottled mice with immunocytochemical technique. This mutant has a genetic defect in copper metabolism and spontaneous neuronal degeneration develops around postnatal day 10, in particular i...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier B.V.
1992
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119898/ https://www.ncbi.nlm.nih.gov/pubmed/1638741 http://dx.doi.org/10.1016/0165-3806(92)90023-P |
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author | Ohno, Masaki Higashi, Yasuto Suzuki, Kinuko |
author_facet | Ohno, Masaki Higashi, Yasuto Suzuki, Kinuko |
author_sort | Ohno, Masaki |
collection | PubMed |
description | Reactive changes of microglia in response to neuronal degeneration were investigated in the brains of brindled mottled mice with immunocytochemical technique. This mutant has a genetic defect in copper metabolism and spontaneous neuronal degeneration develops around postnatal day 10, in particular in the parasagittal regions of the cerebral cortex and thalamus. The antibodies to macrophage specific antigen, F4/80 and to type-three complement receptor, Mac-1 were used for the study. Reactive morphological changes of microglia, which are immuno-reactive to the antibodies to F4/80 and/or Mac-1, were demonstrated in areas corresponding to those of neuronal degeneration, coincident with the emergence of cells expressing major histocompatibility complex class II, Ia, antigen. Some of the Ia expressing cells had morphological features of ramified microglia, while others were rod shaped with few processes and were mostly located in the perivascular regions. The focal nature of such cellular changes suggests that signal(s) from the degenerating neurons may be responsible for microglial activation and cellular expression of the Ia antigen in the brain of the brindled mouse. |
format | Online Article Text |
id | pubmed-7119898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1992 |
publisher | Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71198982020-04-08 Microglial cell response to neuronal degeneration in the brain of brindled mouse Ohno, Masaki Higashi, Yasuto Suzuki, Kinuko Brain Res Dev Brain Res Article Reactive changes of microglia in response to neuronal degeneration were investigated in the brains of brindled mottled mice with immunocytochemical technique. This mutant has a genetic defect in copper metabolism and spontaneous neuronal degeneration develops around postnatal day 10, in particular in the parasagittal regions of the cerebral cortex and thalamus. The antibodies to macrophage specific antigen, F4/80 and to type-three complement receptor, Mac-1 were used for the study. Reactive morphological changes of microglia, which are immuno-reactive to the antibodies to F4/80 and/or Mac-1, were demonstrated in areas corresponding to those of neuronal degeneration, coincident with the emergence of cells expressing major histocompatibility complex class II, Ia, antigen. Some of the Ia expressing cells had morphological features of ramified microglia, while others were rod shaped with few processes and were mostly located in the perivascular regions. The focal nature of such cellular changes suggests that signal(s) from the degenerating neurons may be responsible for microglial activation and cellular expression of the Ia antigen in the brain of the brindled mouse. Published by Elsevier B.V. 1992-05-22 2003-03-14 /pmc/articles/PMC7119898/ /pubmed/1638741 http://dx.doi.org/10.1016/0165-3806(92)90023-P Text en Copyright © 1992 Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Ohno, Masaki Higashi, Yasuto Suzuki, Kinuko Microglial cell response to neuronal degeneration in the brain of brindled mouse |
title | Microglial cell response to neuronal degeneration in the brain of brindled mouse |
title_full | Microglial cell response to neuronal degeneration in the brain of brindled mouse |
title_fullStr | Microglial cell response to neuronal degeneration in the brain of brindled mouse |
title_full_unstemmed | Microglial cell response to neuronal degeneration in the brain of brindled mouse |
title_short | Microglial cell response to neuronal degeneration in the brain of brindled mouse |
title_sort | microglial cell response to neuronal degeneration in the brain of brindled mouse |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119898/ https://www.ncbi.nlm.nih.gov/pubmed/1638741 http://dx.doi.org/10.1016/0165-3806(92)90023-P |
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