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Silver nanoparticles disrupt germline stem cell maintenance in the Drosophila testis

Silver nanoparticles (AgNPs), one of the most popular nanomaterials, are commonly used in consumer products and biomedical devices, despite their potential toxicity. Recently, AgNP exposure was reported to be associated with male reproductive toxicity in mammalian models. However, there is still a l...

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Autores principales: Ong, Cynthia, Lee, Qian Ying, Cai, Yu, Liu, Xiaoli, Ding, Jun, Yung, Lin-Yue Lanry, Bay, Boon-Huat, Baeg, Gyeong-Hun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742918/
https://www.ncbi.nlm.nih.gov/pubmed/26847594
http://dx.doi.org/10.1038/srep20632
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author Ong, Cynthia
Lee, Qian Ying
Cai, Yu
Liu, Xiaoli
Ding, Jun
Yung, Lin-Yue Lanry
Bay, Boon-Huat
Baeg, Gyeong-Hun
author_facet Ong, Cynthia
Lee, Qian Ying
Cai, Yu
Liu, Xiaoli
Ding, Jun
Yung, Lin-Yue Lanry
Bay, Boon-Huat
Baeg, Gyeong-Hun
author_sort Ong, Cynthia
collection PubMed
description Silver nanoparticles (AgNPs), one of the most popular nanomaterials, are commonly used in consumer products and biomedical devices, despite their potential toxicity. Recently, AgNP exposure was reported to be associated with male reproductive toxicity in mammalian models. However, there is still a limited understanding of the effects of AgNPs on spermatogenesis. The fruit fly Drosophila testis is an excellent in vivo model to elucidate the mechanisms underlying AgNP-induced defects in spermatogenesis, as germ lineages can be easily identified and imaged. In this study, we evaluated AgNP-mediated toxicity on spermatogenesis by feeding Drosophila with AgNPs at various concentrations. We first observed a dose-dependent uptake of AgNPs in vivo. Concomitantly, AgNP exposure caused a significant decrease in the viability and delay in the development of Drosophila in a dose-dependent manner. Furthermore, AgNP-treated male flies showed a reduction in fecundity, and the resulting testes contained a decreased number of germline stem cells (GSCs) compared to controls. Interestingly, testes exposed to AgNPs exhibited a dramatic increase in reactive oxygen species levels and showed precocious GSC differentiation. Taken together, our study suggests that AgNP exposure may increase ROS levels in the Drosophila testis, leading to a reduction of GSC number by promoting premature GSC differentiation.
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spelling pubmed-47429182016-02-09 Silver nanoparticles disrupt germline stem cell maintenance in the Drosophila testis Ong, Cynthia Lee, Qian Ying Cai, Yu Liu, Xiaoli Ding, Jun Yung, Lin-Yue Lanry Bay, Boon-Huat Baeg, Gyeong-Hun Sci Rep Article Silver nanoparticles (AgNPs), one of the most popular nanomaterials, are commonly used in consumer products and biomedical devices, despite their potential toxicity. Recently, AgNP exposure was reported to be associated with male reproductive toxicity in mammalian models. However, there is still a limited understanding of the effects of AgNPs on spermatogenesis. The fruit fly Drosophila testis is an excellent in vivo model to elucidate the mechanisms underlying AgNP-induced defects in spermatogenesis, as germ lineages can be easily identified and imaged. In this study, we evaluated AgNP-mediated toxicity on spermatogenesis by feeding Drosophila with AgNPs at various concentrations. We first observed a dose-dependent uptake of AgNPs in vivo. Concomitantly, AgNP exposure caused a significant decrease in the viability and delay in the development of Drosophila in a dose-dependent manner. Furthermore, AgNP-treated male flies showed a reduction in fecundity, and the resulting testes contained a decreased number of germline stem cells (GSCs) compared to controls. Interestingly, testes exposed to AgNPs exhibited a dramatic increase in reactive oxygen species levels and showed precocious GSC differentiation. Taken together, our study suggests that AgNP exposure may increase ROS levels in the Drosophila testis, leading to a reduction of GSC number by promoting premature GSC differentiation. Nature Publishing Group 2016-02-05 /pmc/articles/PMC4742918/ /pubmed/26847594 http://dx.doi.org/10.1038/srep20632 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Ong, Cynthia
Lee, Qian Ying
Cai, Yu
Liu, Xiaoli
Ding, Jun
Yung, Lin-Yue Lanry
Bay, Boon-Huat
Baeg, Gyeong-Hun
Silver nanoparticles disrupt germline stem cell maintenance in the Drosophila testis
title Silver nanoparticles disrupt germline stem cell maintenance in the Drosophila testis
title_full Silver nanoparticles disrupt germline stem cell maintenance in the Drosophila testis
title_fullStr Silver nanoparticles disrupt germline stem cell maintenance in the Drosophila testis
title_full_unstemmed Silver nanoparticles disrupt germline stem cell maintenance in the Drosophila testis
title_short Silver nanoparticles disrupt germline stem cell maintenance in the Drosophila testis
title_sort silver nanoparticles disrupt germline stem cell maintenance in the drosophila testis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742918/
https://www.ncbi.nlm.nih.gov/pubmed/26847594
http://dx.doi.org/10.1038/srep20632
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