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Age-Related Alterations in the Testicular Proteome of a Non-Human Primate
Aging of human testis and associated cellular changes is difficult to assess. Therefore, we used a translational, non-human primate model to get insights into underlying cellular and biochemical processes. Using proteomics and immunohistochemistry, we analyzed testicular tissue of young (age 2 to 3)...
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/PMC8225046/ https://www.ncbi.nlm.nih.gov/pubmed/34074003 http://dx.doi.org/10.3390/cells10061306 |
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author | Stöckl, Jan B. Schmid, Nina Flenkenthaler, Florian Drummer, Charis Behr, Rüdiger Mayerhofer, Artur Arnold, Georg J. Fröhlich, Thomas |
author_facet | Stöckl, Jan B. Schmid, Nina Flenkenthaler, Florian Drummer, Charis Behr, Rüdiger Mayerhofer, Artur Arnold, Georg J. Fröhlich, Thomas |
author_sort | Stöckl, Jan B. |
collection | PubMed |
description | Aging of human testis and associated cellular changes is difficult to assess. Therefore, we used a translational, non-human primate model to get insights into underlying cellular and biochemical processes. Using proteomics and immunohistochemistry, we analyzed testicular tissue of young (age 2 to 3) and old (age 10 to 12) common marmosets (Callithrix jacchus). Using a mass spectrometry-based proteomics approach, we identified 63,124 peptides, which could be assigned to 5924 proteins. Among them, we found proteins specific for germ cells and somatic cells, such as Leydig and Sertoli cells. Quantitative analysis showed 31 differentially abundant proteins, of which 29 proteins were more abundant in older animals. An increased abundance of anti-proliferative proteins, among them CDKN2A, indicate reduced cell proliferation in old testes. Additionally, an increased abundance of several small leucine rich repeat proteoglycans and other extracellular matrix proteins was observed, which may be related to impaired cell migration and fibrotic events. Furthermore, an increased abundance of proteins with inhibitory roles in smooth muscle cell contraction like CNN1 indicates functional alterations in testicular peritubular cells and may mirror a reduced capacity of these cells to contract in old testes. |
format | Online Article Text |
id | pubmed-8225046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82250462021-06-25 Age-Related Alterations in the Testicular Proteome of a Non-Human Primate Stöckl, Jan B. Schmid, Nina Flenkenthaler, Florian Drummer, Charis Behr, Rüdiger Mayerhofer, Artur Arnold, Georg J. Fröhlich, Thomas Cells Article Aging of human testis and associated cellular changes is difficult to assess. Therefore, we used a translational, non-human primate model to get insights into underlying cellular and biochemical processes. Using proteomics and immunohistochemistry, we analyzed testicular tissue of young (age 2 to 3) and old (age 10 to 12) common marmosets (Callithrix jacchus). Using a mass spectrometry-based proteomics approach, we identified 63,124 peptides, which could be assigned to 5924 proteins. Among them, we found proteins specific for germ cells and somatic cells, such as Leydig and Sertoli cells. Quantitative analysis showed 31 differentially abundant proteins, of which 29 proteins were more abundant in older animals. An increased abundance of anti-proliferative proteins, among them CDKN2A, indicate reduced cell proliferation in old testes. Additionally, an increased abundance of several small leucine rich repeat proteoglycans and other extracellular matrix proteins was observed, which may be related to impaired cell migration and fibrotic events. Furthermore, an increased abundance of proteins with inhibitory roles in smooth muscle cell contraction like CNN1 indicates functional alterations in testicular peritubular cells and may mirror a reduced capacity of these cells to contract in old testes. MDPI 2021-05-24 /pmc/articles/PMC8225046/ /pubmed/34074003 http://dx.doi.org/10.3390/cells10061306 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Stöckl, Jan B. Schmid, Nina Flenkenthaler, Florian Drummer, Charis Behr, Rüdiger Mayerhofer, Artur Arnold, Georg J. Fröhlich, Thomas Age-Related Alterations in the Testicular Proteome of a Non-Human Primate |
title | Age-Related Alterations in the Testicular Proteome of a Non-Human Primate |
title_full | Age-Related Alterations in the Testicular Proteome of a Non-Human Primate |
title_fullStr | Age-Related Alterations in the Testicular Proteome of a Non-Human Primate |
title_full_unstemmed | Age-Related Alterations in the Testicular Proteome of a Non-Human Primate |
title_short | Age-Related Alterations in the Testicular Proteome of a Non-Human Primate |
title_sort | age-related alterations in the testicular proteome of a non-human primate |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225046/ https://www.ncbi.nlm.nih.gov/pubmed/34074003 http://dx.doi.org/10.3390/cells10061306 |
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