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Chronic Porphyromonas gingivalis infection accelerates the occurrence of age-related granules in ApoE(–) (/) (–) mice brains

This study explored the origin of age-related granules in the apolipoprotein E gene knockout (ApoE(−/−)) B6 background mice brains following chronic gingival infection with Porphyromonas gingivalis for 24 weeks. Intracerebral localization of P. gingivalis was detected by fluorescence in situ hybridi...

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Autores principales: Singhrao, Sim K., Chukkapalli, Sasanka, Poole, Sophie, Velsko, Irina, Crean, St John, Kesavalu, Lakshmyya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5328363/
https://www.ncbi.nlm.nih.gov/pubmed/28326151
http://dx.doi.org/10.1080/20002297.2016.1270602
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author Singhrao, Sim K.
Chukkapalli, Sasanka
Poole, Sophie
Velsko, Irina
Crean, St John
Kesavalu, Lakshmyya
author_facet Singhrao, Sim K.
Chukkapalli, Sasanka
Poole, Sophie
Velsko, Irina
Crean, St John
Kesavalu, Lakshmyya
author_sort Singhrao, Sim K.
collection PubMed
description This study explored the origin of age-related granules in the apolipoprotein E gene knockout (ApoE(−/−)) B6 background mice brains following chronic gingival infection with Porphyromonas gingivalis for 24 weeks. Intracerebral localization of P. gingivalis was detected by fluorescence in situ hybridization (FISH) and its protease by immunohistochemistry. The age-related granules were observed by periodic acid–Schiff (PAS), silver impregnation, and immunostaining. FISH showed intracerebral dissemination of P. gingivalis cells (p = 0.001). PAS and silver impregnation demonstrated the presence of larger inclusions restricted to the CA1, CA2, and dentate gyrus sectors of the hippocampus. A specific monoclonal antibody to bacterial peptidoglycan detected clusters of granules with variable sizes in mice brains infected with P. gingivalis (p = 0.004), and also highlighted areas of diffuse punctate staining equating to physical tissue damage. Mouse immunoglobulin G was observed in the capillaries of the cerebral parenchyma of all P. gingivalis–infected brains (p = 0.001), and on pyramidal neurons in some severely affected mice, compared with the sham-infected mice. Gingipains was also observed in microvessels of the hippocampus in the infected mice. This study supports the possibility of early appearance of age-related granules in ApoE(−/−) mice following inflammation-mediated tissue injury, accompanied by loss of cerebral blood-brain barrier integrity.
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spelling pubmed-53283632017-03-06 Chronic Porphyromonas gingivalis infection accelerates the occurrence of age-related granules in ApoE(–) (/) (–) mice brains Singhrao, Sim K. Chukkapalli, Sasanka Poole, Sophie Velsko, Irina Crean, St John Kesavalu, Lakshmyya J Oral Microbiol Original Articles This study explored the origin of age-related granules in the apolipoprotein E gene knockout (ApoE(−/−)) B6 background mice brains following chronic gingival infection with Porphyromonas gingivalis for 24 weeks. Intracerebral localization of P. gingivalis was detected by fluorescence in situ hybridization (FISH) and its protease by immunohistochemistry. The age-related granules were observed by periodic acid–Schiff (PAS), silver impregnation, and immunostaining. FISH showed intracerebral dissemination of P. gingivalis cells (p = 0.001). PAS and silver impregnation demonstrated the presence of larger inclusions restricted to the CA1, CA2, and dentate gyrus sectors of the hippocampus. A specific monoclonal antibody to bacterial peptidoglycan detected clusters of granules with variable sizes in mice brains infected with P. gingivalis (p = 0.004), and also highlighted areas of diffuse punctate staining equating to physical tissue damage. Mouse immunoglobulin G was observed in the capillaries of the cerebral parenchyma of all P. gingivalis–infected brains (p = 0.001), and on pyramidal neurons in some severely affected mice, compared with the sham-infected mice. Gingipains was also observed in microvessels of the hippocampus in the infected mice. This study supports the possibility of early appearance of age-related granules in ApoE(−/−) mice following inflammation-mediated tissue injury, accompanied by loss of cerebral blood-brain barrier integrity. Taylor & Francis 2017-01-17 /pmc/articles/PMC5328363/ /pubmed/28326151 http://dx.doi.org/10.1080/20002297.2016.1270602 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Singhrao, Sim K.
Chukkapalli, Sasanka
Poole, Sophie
Velsko, Irina
Crean, St John
Kesavalu, Lakshmyya
Chronic Porphyromonas gingivalis infection accelerates the occurrence of age-related granules in ApoE(–) (/) (–) mice brains
title Chronic Porphyromonas gingivalis infection accelerates the occurrence of age-related granules in ApoE(–) (/) (–) mice brains
title_full Chronic Porphyromonas gingivalis infection accelerates the occurrence of age-related granules in ApoE(–) (/) (–) mice brains
title_fullStr Chronic Porphyromonas gingivalis infection accelerates the occurrence of age-related granules in ApoE(–) (/) (–) mice brains
title_full_unstemmed Chronic Porphyromonas gingivalis infection accelerates the occurrence of age-related granules in ApoE(–) (/) (–) mice brains
title_short Chronic Porphyromonas gingivalis infection accelerates the occurrence of age-related granules in ApoE(–) (/) (–) mice brains
title_sort chronic porphyromonas gingivalis infection accelerates the occurrence of age-related granules in apoe(–) (/) (–) mice brains
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5328363/
https://www.ncbi.nlm.nih.gov/pubmed/28326151
http://dx.doi.org/10.1080/20002297.2016.1270602
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