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Reproductive toxicity and gender differences induced by cadmium telluride quantum dots in an invertebrate model organism
Sexual glands are key sites affected by nanotoxicity, but there is no sensitive assay for measuring reproductive toxicity in animals. The aim of this study was to investigate the toxic effects of cadmium telluride quantum dots (CdTe-QDs) on gonads in a model organism, Bombyx mori. After dorsal vein...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037452/ https://www.ncbi.nlm.nih.gov/pubmed/27669995 http://dx.doi.org/10.1038/srep34182 |
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author | Yan, Si-Qi Xing, Rui Zhou, Yan-Feng Li, Kai-Le Su, Yuan-Yuan Qiu, Jian-Feng Zhang, Yun-Hu Zhang, Ke-Qin He, Yao Lu, Xiao-Ping Xu, Shi-Qing |
author_facet | Yan, Si-Qi Xing, Rui Zhou, Yan-Feng Li, Kai-Le Su, Yuan-Yuan Qiu, Jian-Feng Zhang, Yun-Hu Zhang, Ke-Qin He, Yao Lu, Xiao-Ping Xu, Shi-Qing |
author_sort | Yan, Si-Qi |
collection | PubMed |
description | Sexual glands are key sites affected by nanotoxicity, but there is no sensitive assay for measuring reproductive toxicity in animals. The aim of this study was to investigate the toxic effects of cadmium telluride quantum dots (CdTe-QDs) on gonads in a model organism, Bombyx mori. After dorsal vein injection of 0.32 nmol of CdTe-QDs per individual, the QDs passed through the outer membranes of gonads via the generation of ROS in the membranes of spermatocysts and ovarioles, as well as internal germ cells, thereby inducing early germ cell death or malformations via complex mechanisms related to apoptosis and autophagy through mitochondrial and lysosomal pathways. Histological observations of the gonads and quantitative analyses of germ cell development showed that the reproductive toxicity was characterized by obvious male sensitivity. Exposure to QDs in the early stage of males had severe adverse effects on the quantity and quality of sperm, which was the main reason for the occurrence of unfertilized eggs. Ala- or Gly-conjugated QDs could reduce the nanotoxicity of CdTe-QDs during germ cell development and fertilization of their offspring. The results demonstrate that males are preferable models for evaluating the reproductive toxicity of QDs in combined in vivo/in vitro investigations. |
format | Online Article Text |
id | pubmed-5037452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50374522016-09-30 Reproductive toxicity and gender differences induced by cadmium telluride quantum dots in an invertebrate model organism Yan, Si-Qi Xing, Rui Zhou, Yan-Feng Li, Kai-Le Su, Yuan-Yuan Qiu, Jian-Feng Zhang, Yun-Hu Zhang, Ke-Qin He, Yao Lu, Xiao-Ping Xu, Shi-Qing Sci Rep Article Sexual glands are key sites affected by nanotoxicity, but there is no sensitive assay for measuring reproductive toxicity in animals. The aim of this study was to investigate the toxic effects of cadmium telluride quantum dots (CdTe-QDs) on gonads in a model organism, Bombyx mori. After dorsal vein injection of 0.32 nmol of CdTe-QDs per individual, the QDs passed through the outer membranes of gonads via the generation of ROS in the membranes of spermatocysts and ovarioles, as well as internal germ cells, thereby inducing early germ cell death or malformations via complex mechanisms related to apoptosis and autophagy through mitochondrial and lysosomal pathways. Histological observations of the gonads and quantitative analyses of germ cell development showed that the reproductive toxicity was characterized by obvious male sensitivity. Exposure to QDs in the early stage of males had severe adverse effects on the quantity and quality of sperm, which was the main reason for the occurrence of unfertilized eggs. Ala- or Gly-conjugated QDs could reduce the nanotoxicity of CdTe-QDs during germ cell development and fertilization of their offspring. The results demonstrate that males are preferable models for evaluating the reproductive toxicity of QDs in combined in vivo/in vitro investigations. Nature Publishing Group 2016-09-27 /pmc/articles/PMC5037452/ /pubmed/27669995 http://dx.doi.org/10.1038/srep34182 Text en Copyright © 2016, The Author(s) 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 Yan, Si-Qi Xing, Rui Zhou, Yan-Feng Li, Kai-Le Su, Yuan-Yuan Qiu, Jian-Feng Zhang, Yun-Hu Zhang, Ke-Qin He, Yao Lu, Xiao-Ping Xu, Shi-Qing Reproductive toxicity and gender differences induced by cadmium telluride quantum dots in an invertebrate model organism |
title | Reproductive toxicity and gender differences induced by cadmium telluride quantum dots in an invertebrate model organism |
title_full | Reproductive toxicity and gender differences induced by cadmium telluride quantum dots in an invertebrate model organism |
title_fullStr | Reproductive toxicity and gender differences induced by cadmium telluride quantum dots in an invertebrate model organism |
title_full_unstemmed | Reproductive toxicity and gender differences induced by cadmium telluride quantum dots in an invertebrate model organism |
title_short | Reproductive toxicity and gender differences induced by cadmium telluride quantum dots in an invertebrate model organism |
title_sort | reproductive toxicity and gender differences induced by cadmium telluride quantum dots in an invertebrate model organism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037452/ https://www.ncbi.nlm.nih.gov/pubmed/27669995 http://dx.doi.org/10.1038/srep34182 |
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