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No evidence for age-related alterations in the marmoset retina
The physiological aging process of the retina is accompanied by various and sometimes extensive changes: Macular degeneration, retinopathies and glaucoma are the most common findings in the elderly and can potentially lead to irreversible visual disablements up to blindness. To study the aging proce...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9479465/ https://www.ncbi.nlm.nih.gov/pubmed/36120100 http://dx.doi.org/10.3389/fnana.2022.945295 |
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author | Haverkamp, Silke Reinhard, Katja Peichl, Leo Mietsch, Matthias |
author_facet | Haverkamp, Silke Reinhard, Katja Peichl, Leo Mietsch, Matthias |
author_sort | Haverkamp, Silke |
collection | PubMed |
description | The physiological aging process of the retina is accompanied by various and sometimes extensive changes: Macular degeneration, retinopathies and glaucoma are the most common findings in the elderly and can potentially lead to irreversible visual disablements up to blindness. To study the aging process and to identify possible therapeutic targets to counteract these diseases, the use of appropriate animal models is mandatory. Besides the most commonly used rodent species, a non-human primate, the common marmoset (Callithrix jacchus) emerged as a promising animal model of human aging over the last years. However, the visual aging process in this species is only partially characterized, especially with regard to retinal aberrations. Therefore, we assessed here for the first time potential changes in retinal morphology of the common marmoset of different age groups. By cell type specific immunolabeling, we analyzed different cell types and distributions, potential photoreceptor and ganglion cell loss, and structural reorganization. We detected no signs of age-related differences in staining patterns or densities of various cell populations. For example, there were no signs of photoreceptor degeneration, and there was only minimal sprouting of rod bipolar cells in aged retinas. Altogether, we describe here the maintenance of a stable neuronal architecture, distribution and number of different cell populations with only mild aberrations during the aging process in the common marmoset retina. These findings are in stark contrast to previously reported findings in rodent species and humans and deserve further investigations to identify the underlying mechanisms and possible therapeutic targets. |
format | Online Article Text |
id | pubmed-9479465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94794652022-09-17 No evidence for age-related alterations in the marmoset retina Haverkamp, Silke Reinhard, Katja Peichl, Leo Mietsch, Matthias Front Neuroanat Neuroanatomy The physiological aging process of the retina is accompanied by various and sometimes extensive changes: Macular degeneration, retinopathies and glaucoma are the most common findings in the elderly and can potentially lead to irreversible visual disablements up to blindness. To study the aging process and to identify possible therapeutic targets to counteract these diseases, the use of appropriate animal models is mandatory. Besides the most commonly used rodent species, a non-human primate, the common marmoset (Callithrix jacchus) emerged as a promising animal model of human aging over the last years. However, the visual aging process in this species is only partially characterized, especially with regard to retinal aberrations. Therefore, we assessed here for the first time potential changes in retinal morphology of the common marmoset of different age groups. By cell type specific immunolabeling, we analyzed different cell types and distributions, potential photoreceptor and ganglion cell loss, and structural reorganization. We detected no signs of age-related differences in staining patterns or densities of various cell populations. For example, there were no signs of photoreceptor degeneration, and there was only minimal sprouting of rod bipolar cells in aged retinas. Altogether, we describe here the maintenance of a stable neuronal architecture, distribution and number of different cell populations with only mild aberrations during the aging process in the common marmoset retina. These findings are in stark contrast to previously reported findings in rodent species and humans and deserve further investigations to identify the underlying mechanisms and possible therapeutic targets. Frontiers Media S.A. 2022-09-02 /pmc/articles/PMC9479465/ /pubmed/36120100 http://dx.doi.org/10.3389/fnana.2022.945295 Text en Copyright © 2022 Haverkamp, Reinhard, Peichl and Mietsch. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroanatomy Haverkamp, Silke Reinhard, Katja Peichl, Leo Mietsch, Matthias No evidence for age-related alterations in the marmoset retina |
title | No evidence for age-related alterations in the marmoset retina |
title_full | No evidence for age-related alterations in the marmoset retina |
title_fullStr | No evidence for age-related alterations in the marmoset retina |
title_full_unstemmed | No evidence for age-related alterations in the marmoset retina |
title_short | No evidence for age-related alterations in the marmoset retina |
title_sort | no evidence for age-related alterations in the marmoset retina |
topic | Neuroanatomy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9479465/ https://www.ncbi.nlm.nih.gov/pubmed/36120100 http://dx.doi.org/10.3389/fnana.2022.945295 |
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