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Exacerbation of AMD Phenotype in Lasered CNV Murine Model by Dysbiotic Oral Pathogens
Emerging evidence underscores an association between age-related macular degeneration (AMD) and periodontal disease (PD), yet the biological basis of this linkage and the specific role of oral dysbiosis caused by PD in AMD pathophysiology remains unclear. Furthermore, a simple reproducible model tha...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922506/ https://www.ncbi.nlm.nih.gov/pubmed/33670526 http://dx.doi.org/10.3390/antiox10020309 |
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author | Arjunan, Pachiappan Swaminathan, Radhika Yuan, Jessie Elashiry, Mohamed Tawfik, Amany Al-Shabrawey, Mohamed Martin, Pamela M. Muthusamy, Thangaraju Cutler, Christopher W. |
author_facet | Arjunan, Pachiappan Swaminathan, Radhika Yuan, Jessie Elashiry, Mohamed Tawfik, Amany Al-Shabrawey, Mohamed Martin, Pamela M. Muthusamy, Thangaraju Cutler, Christopher W. |
author_sort | Arjunan, Pachiappan |
collection | PubMed |
description | Emerging evidence underscores an association between age-related macular degeneration (AMD) and periodontal disease (PD), yet the biological basis of this linkage and the specific role of oral dysbiosis caused by PD in AMD pathophysiology remains unclear. Furthermore, a simple reproducible model that emulates characteristics of both AMD and PD has been lacking. Hence, we established a novel AMD+PD murine model to decipher the potential role of oral infection (ligature-enhanced) with the keystone periodontal pathogen Porphyromonas gingivalis, in the progression of neovasculogenesis in a laser-induced choroidal-neovascularization (Li-CNV) mouse retina. By a combination of fundus photography, optical coherence tomography, and fluorescein angiography, we documented inflammatory drusen-like lesions, reduced retinal thickness, and increased vascular leakage in AMD+PD mice retinae. H&E further confirmed a significant reduction of retinal thickness and subretinal drusen-like deposits. Immunofluorescence microscopy revealed significant induction of choroidal/retinal vasculogenesis in AMD+PD mice. qPCR identified increased expression of oxidative-stress, angiogenesis, pro-inflammatory mediators, whereas antioxidants and anti-inflammatory genes in AMD+PD mice retinae were notably decreased. Through qPCR, we detected Pg and its fimbrial 16s-RrNA gene expression in the AMD+PD mice retinae. To sum-up, this is the first in vivo study signifying a role of periodontal infection in augmentation of AMD phenotype, with the aid of a pioneering AMD+PD murine model established in our laboratory. |
format | Online Article Text |
id | pubmed-7922506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79225062021-03-03 Exacerbation of AMD Phenotype in Lasered CNV Murine Model by Dysbiotic Oral Pathogens Arjunan, Pachiappan Swaminathan, Radhika Yuan, Jessie Elashiry, Mohamed Tawfik, Amany Al-Shabrawey, Mohamed Martin, Pamela M. Muthusamy, Thangaraju Cutler, Christopher W. Antioxidants (Basel) Article Emerging evidence underscores an association between age-related macular degeneration (AMD) and periodontal disease (PD), yet the biological basis of this linkage and the specific role of oral dysbiosis caused by PD in AMD pathophysiology remains unclear. Furthermore, a simple reproducible model that emulates characteristics of both AMD and PD has been lacking. Hence, we established a novel AMD+PD murine model to decipher the potential role of oral infection (ligature-enhanced) with the keystone periodontal pathogen Porphyromonas gingivalis, in the progression of neovasculogenesis in a laser-induced choroidal-neovascularization (Li-CNV) mouse retina. By a combination of fundus photography, optical coherence tomography, and fluorescein angiography, we documented inflammatory drusen-like lesions, reduced retinal thickness, and increased vascular leakage in AMD+PD mice retinae. H&E further confirmed a significant reduction of retinal thickness and subretinal drusen-like deposits. Immunofluorescence microscopy revealed significant induction of choroidal/retinal vasculogenesis in AMD+PD mice. qPCR identified increased expression of oxidative-stress, angiogenesis, pro-inflammatory mediators, whereas antioxidants and anti-inflammatory genes in AMD+PD mice retinae were notably decreased. Through qPCR, we detected Pg and its fimbrial 16s-RrNA gene expression in the AMD+PD mice retinae. To sum-up, this is the first in vivo study signifying a role of periodontal infection in augmentation of AMD phenotype, with the aid of a pioneering AMD+PD murine model established in our laboratory. MDPI 2021-02-18 /pmc/articles/PMC7922506/ /pubmed/33670526 http://dx.doi.org/10.3390/antiox10020309 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Arjunan, Pachiappan Swaminathan, Radhika Yuan, Jessie Elashiry, Mohamed Tawfik, Amany Al-Shabrawey, Mohamed Martin, Pamela M. Muthusamy, Thangaraju Cutler, Christopher W. Exacerbation of AMD Phenotype in Lasered CNV Murine Model by Dysbiotic Oral Pathogens |
title | Exacerbation of AMD Phenotype in Lasered CNV Murine Model by Dysbiotic Oral Pathogens |
title_full | Exacerbation of AMD Phenotype in Lasered CNV Murine Model by Dysbiotic Oral Pathogens |
title_fullStr | Exacerbation of AMD Phenotype in Lasered CNV Murine Model by Dysbiotic Oral Pathogens |
title_full_unstemmed | Exacerbation of AMD Phenotype in Lasered CNV Murine Model by Dysbiotic Oral Pathogens |
title_short | Exacerbation of AMD Phenotype in Lasered CNV Murine Model by Dysbiotic Oral Pathogens |
title_sort | exacerbation of amd phenotype in lasered cnv murine model by dysbiotic oral pathogens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922506/ https://www.ncbi.nlm.nih.gov/pubmed/33670526 http://dx.doi.org/10.3390/antiox10020309 |
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