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Reproduction disrupts stem cell homeostasis in testes of aged male Drosophila via an induced microenvironment
Stem cells rely on instructive cues from their environment. Alterations in microenvironments might contribute to tissue dysfunction and disease pathogenesis. Germline stem cells (GSCs) and cyst stem cells (CySC) in Drosophila testes are normally maintained in the apical area by the testicular hub. I...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6622487/ https://www.ncbi.nlm.nih.gov/pubmed/31295251 http://dx.doi.org/10.1371/journal.pgen.1008062 |
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author | Chang, Yi Chieh Tu, Hsin Chen, Jing-Yi Chang, Ching-Chin Yang, Shu Yuan Pi, Haiwei |
author_facet | Chang, Yi Chieh Tu, Hsin Chen, Jing-Yi Chang, Ching-Chin Yang, Shu Yuan Pi, Haiwei |
author_sort | Chang, Yi Chieh |
collection | PubMed |
description | Stem cells rely on instructive cues from their environment. Alterations in microenvironments might contribute to tissue dysfunction and disease pathogenesis. Germline stem cells (GSCs) and cyst stem cells (CySC) in Drosophila testes are normally maintained in the apical area by the testicular hub. In this study, we found that reproduction leads to accumulation of early differentiating daughters of CySCs and GSCs in the testes of aged male flies, due to hyperactivation of Jun-N-terminal kinase (JNK) signaling to maintain self-renewal gene expression in the differentiating cyst cells. JNK activity is normally required to maintain CySCs in the apical niche. A muscle sheath surrounds the Drosophila testis to maintain its long coiled structure. Importantly, reproduction triggers accumulation of the tumor necrosis factor (TNF) Eiger in the testis muscle to activate JNK signaling via the TNF receptor Grindelwald in the cyst cells. Reducing Eiger activity in the testis muscle sheath suppressed reproduction-induced differentiation defects, but had little effect on testis homeostasis of unmated males. Our results reveal that reproduction in males provokes a dramatic shift in the testicular microenvironment, which impairs tissue homeostasis and spermatogenesis in the testes. |
format | Online Article Text |
id | pubmed-6622487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-66224872019-07-25 Reproduction disrupts stem cell homeostasis in testes of aged male Drosophila via an induced microenvironment Chang, Yi Chieh Tu, Hsin Chen, Jing-Yi Chang, Ching-Chin Yang, Shu Yuan Pi, Haiwei PLoS Genet Research Article Stem cells rely on instructive cues from their environment. Alterations in microenvironments might contribute to tissue dysfunction and disease pathogenesis. Germline stem cells (GSCs) and cyst stem cells (CySC) in Drosophila testes are normally maintained in the apical area by the testicular hub. In this study, we found that reproduction leads to accumulation of early differentiating daughters of CySCs and GSCs in the testes of aged male flies, due to hyperactivation of Jun-N-terminal kinase (JNK) signaling to maintain self-renewal gene expression in the differentiating cyst cells. JNK activity is normally required to maintain CySCs in the apical niche. A muscle sheath surrounds the Drosophila testis to maintain its long coiled structure. Importantly, reproduction triggers accumulation of the tumor necrosis factor (TNF) Eiger in the testis muscle to activate JNK signaling via the TNF receptor Grindelwald in the cyst cells. Reducing Eiger activity in the testis muscle sheath suppressed reproduction-induced differentiation defects, but had little effect on testis homeostasis of unmated males. Our results reveal that reproduction in males provokes a dramatic shift in the testicular microenvironment, which impairs tissue homeostasis and spermatogenesis in the testes. Public Library of Science 2019-07-11 /pmc/articles/PMC6622487/ /pubmed/31295251 http://dx.doi.org/10.1371/journal.pgen.1008062 Text en © 2019 Chang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Chang, Yi Chieh Tu, Hsin Chen, Jing-Yi Chang, Ching-Chin Yang, Shu Yuan Pi, Haiwei Reproduction disrupts stem cell homeostasis in testes of aged male Drosophila via an induced microenvironment |
title | Reproduction disrupts stem cell homeostasis in testes of aged male Drosophila via an induced microenvironment |
title_full | Reproduction disrupts stem cell homeostasis in testes of aged male Drosophila via an induced microenvironment |
title_fullStr | Reproduction disrupts stem cell homeostasis in testes of aged male Drosophila via an induced microenvironment |
title_full_unstemmed | Reproduction disrupts stem cell homeostasis in testes of aged male Drosophila via an induced microenvironment |
title_short | Reproduction disrupts stem cell homeostasis in testes of aged male Drosophila via an induced microenvironment |
title_sort | reproduction disrupts stem cell homeostasis in testes of aged male drosophila via an induced microenvironment |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6622487/ https://www.ncbi.nlm.nih.gov/pubmed/31295251 http://dx.doi.org/10.1371/journal.pgen.1008062 |
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