Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Chang, Yi Chieh, Tu, Hsin, Chen, Jing-Yi, Chang, Ching-Chin, Yang, Shu Yuan, Pi, Haiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
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
_version_ 1783434164694941696
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
work_keys_str_mv AT changyichieh reproductiondisruptsstemcellhomeostasisintestesofagedmaledrosophilaviaaninducedmicroenvironment
AT tuhsin reproductiondisruptsstemcellhomeostasisintestesofagedmaledrosophilaviaaninducedmicroenvironment
AT chenjingyi reproductiondisruptsstemcellhomeostasisintestesofagedmaledrosophilaviaaninducedmicroenvironment
AT changchingchin reproductiondisruptsstemcellhomeostasisintestesofagedmaledrosophilaviaaninducedmicroenvironment
AT yangshuyuan reproductiondisruptsstemcellhomeostasisintestesofagedmaledrosophilaviaaninducedmicroenvironment
AT pihaiwei reproductiondisruptsstemcellhomeostasisintestesofagedmaledrosophilaviaaninducedmicroenvironment