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Internalization of silver nanoparticles into mouse spermatozoa results in poor fertilization and compromised embryo development

Silver nanoparticles (AgNPs) have many features that make them attractive as medical devices, especially in therapeutic agents and drug delivery systems. Here we have introduced AgNPs into mouse spermatozoa and then determined the cytotoxic effects of AgNPs on sperm function and subsequent embryo de...

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Autores principales: Yoisungnern, Ton, Choi, Yun-Jung, Woong Han, Jae, Kang, Min-Hee, Das, Joydeep, Gurunathan, Sangiliyandi, Kwon, Deug-Nam, Cho, Ssang-Goo, Park, Chankyu, Kyung Chang, Won, Chang, Byung-Soo, Parnpai, Rangsun, Kim, Jin-Hoi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459204/
https://www.ncbi.nlm.nih.gov/pubmed/26054035
http://dx.doi.org/10.1038/srep11170
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author Yoisungnern, Ton
Choi, Yun-Jung
Woong Han, Jae
Kang, Min-Hee
Das, Joydeep
Gurunathan, Sangiliyandi
Kwon, Deug-Nam
Cho, Ssang-Goo
Park, Chankyu
Kyung Chang, Won
Chang, Byung-Soo
Parnpai, Rangsun
Kim, Jin-Hoi
author_facet Yoisungnern, Ton
Choi, Yun-Jung
Woong Han, Jae
Kang, Min-Hee
Das, Joydeep
Gurunathan, Sangiliyandi
Kwon, Deug-Nam
Cho, Ssang-Goo
Park, Chankyu
Kyung Chang, Won
Chang, Byung-Soo
Parnpai, Rangsun
Kim, Jin-Hoi
author_sort Yoisungnern, Ton
collection PubMed
description Silver nanoparticles (AgNPs) have many features that make them attractive as medical devices, especially in therapeutic agents and drug delivery systems. Here we have introduced AgNPs into mouse spermatozoa and then determined the cytotoxic effects of AgNPs on sperm function and subsequent embryo development. Scanning electron microscopy and transmission electron microscopy analyses showed that AgNPs could be internalized into sperm cells. Furthermore, exposure to AgNPs inhibited sperm viability and the acrosome reaction in a dose-dependent manner, whereas sperm mitochondrial copy numbers, morphological abnormalities, and mortality due to reactive oxygen species were significantly increased. Likewise, sperm abnormalities due to AgNPs internalization significantly decreased the rate of oocyte fertilization and blastocyst formation. Blastocysts obtained from AgNPs-treated spermatozoa showed lower expression of trophectoderm-associated and pluripotent marker genes. Overall, we propose that AgNPs internalization into spermatozoa may alter sperm physiology, leading to poor fertilization and embryonic development. Such AgNPs-induced reprotoxicity may be a valuable tool as models for testing the safety and applicability of medical devices using AgNPs.
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spelling pubmed-44592042015-06-17 Internalization of silver nanoparticles into mouse spermatozoa results in poor fertilization and compromised embryo development Yoisungnern, Ton Choi, Yun-Jung Woong Han, Jae Kang, Min-Hee Das, Joydeep Gurunathan, Sangiliyandi Kwon, Deug-Nam Cho, Ssang-Goo Park, Chankyu Kyung Chang, Won Chang, Byung-Soo Parnpai, Rangsun Kim, Jin-Hoi Sci Rep Article Silver nanoparticles (AgNPs) have many features that make them attractive as medical devices, especially in therapeutic agents and drug delivery systems. Here we have introduced AgNPs into mouse spermatozoa and then determined the cytotoxic effects of AgNPs on sperm function and subsequent embryo development. Scanning electron microscopy and transmission electron microscopy analyses showed that AgNPs could be internalized into sperm cells. Furthermore, exposure to AgNPs inhibited sperm viability and the acrosome reaction in a dose-dependent manner, whereas sperm mitochondrial copy numbers, morphological abnormalities, and mortality due to reactive oxygen species were significantly increased. Likewise, sperm abnormalities due to AgNPs internalization significantly decreased the rate of oocyte fertilization and blastocyst formation. Blastocysts obtained from AgNPs-treated spermatozoa showed lower expression of trophectoderm-associated and pluripotent marker genes. Overall, we propose that AgNPs internalization into spermatozoa may alter sperm physiology, leading to poor fertilization and embryonic development. Such AgNPs-induced reprotoxicity may be a valuable tool as models for testing the safety and applicability of medical devices using AgNPs. Nature Publishing Group 2015-06-08 /pmc/articles/PMC4459204/ /pubmed/26054035 http://dx.doi.org/10.1038/srep11170 Text en Copyright © 2015, 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
Yoisungnern, Ton
Choi, Yun-Jung
Woong Han, Jae
Kang, Min-Hee
Das, Joydeep
Gurunathan, Sangiliyandi
Kwon, Deug-Nam
Cho, Ssang-Goo
Park, Chankyu
Kyung Chang, Won
Chang, Byung-Soo
Parnpai, Rangsun
Kim, Jin-Hoi
Internalization of silver nanoparticles into mouse spermatozoa results in poor fertilization and compromised embryo development
title Internalization of silver nanoparticles into mouse spermatozoa results in poor fertilization and compromised embryo development
title_full Internalization of silver nanoparticles into mouse spermatozoa results in poor fertilization and compromised embryo development
title_fullStr Internalization of silver nanoparticles into mouse spermatozoa results in poor fertilization and compromised embryo development
title_full_unstemmed Internalization of silver nanoparticles into mouse spermatozoa results in poor fertilization and compromised embryo development
title_short Internalization of silver nanoparticles into mouse spermatozoa results in poor fertilization and compromised embryo development
title_sort internalization of silver nanoparticles into mouse spermatozoa results in poor fertilization and compromised embryo development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459204/
https://www.ncbi.nlm.nih.gov/pubmed/26054035
http://dx.doi.org/10.1038/srep11170
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