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The Invasion and Reproductive Toxicity of QDs-Transferrin Bioconjugates on Preantral Follicle in vitro

The toxicity of QD has been extensively studied over the past decade. However, the potential toxicity of QDs impedes its use for clinical research. In this work, we established a preantral follicle in vitro culture system to investigate the effects of QD-Transferrin (QDs-Tf) bioconjugates on follicl...

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Autores principales: Xu, Gaixia, Lin, Suxia, Law, Wing-Cheung, Roy, Indrajit, Lin, Xiaotan, Mei, Shujiang, Ma, Hanwu, Chen, Siping, Niu, Hanben, Wang, Xiaomei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425092/
https://www.ncbi.nlm.nih.gov/pubmed/22916073
http://dx.doi.org/10.7150/thno.4290
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author Xu, Gaixia
Lin, Suxia
Law, Wing-Cheung
Roy, Indrajit
Lin, Xiaotan
Mei, Shujiang
Ma, Hanwu
Chen, Siping
Niu, Hanben
Wang, Xiaomei
author_facet Xu, Gaixia
Lin, Suxia
Law, Wing-Cheung
Roy, Indrajit
Lin, Xiaotan
Mei, Shujiang
Ma, Hanwu
Chen, Siping
Niu, Hanben
Wang, Xiaomei
author_sort Xu, Gaixia
collection PubMed
description The toxicity of QD has been extensively studied over the past decade. However, the potential toxicity of QDs impedes its use for clinical research. In this work, we established a preantral follicle in vitro culture system to investigate the effects of QD-Transferrin (QDs-Tf) bioconjugates on follicle development and oocyte maturation. The preantral follicles were cultured and exposed to CdTe/ZnTe QDs-Tf bioconjugates with various concentrations and the reproductive toxicity was assessed at different time points post-treatment. The invasion of QDs-Tf for oocytes was verified by laser scanning confocal microscope. Steroid production was evaluated by immunoassay. C-band Giemsa staining was performed to observe the chromosome abnormality of oocytes. The results showed that the QDs-Tf bioconjugates could permeate into granulosa cells and theca cells, but not into oocyte. There are no obvious changes of oocyte diameter, the mucification of cumulus-oocyte-complexes and the occurrence of aneulpoidy as compared with the control group. However, delay in the antrum formation and decrease in the ratio of oocytes with first polar body were observed in QDs-Tf-treated groups. The matured oocytes with first polar body decreased significantly by ~16% (from 79.6±10 % to 63±2.9 %) when the concentration of QDs-Tf bioconjugates exceeded 2.89 nmol·L(-1) (P < 0.05). Our results implied that the CdTe/ZnTe QDs-Tf bioconjugates were reproductive toxic for follicle development, and thus also revealed that this in vitro culture system of preantral follicle is a highly sensitive tool for study on the reproductive toxicity of nanoparticles.
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spelling pubmed-34250922012-08-22 The Invasion and Reproductive Toxicity of QDs-Transferrin Bioconjugates on Preantral Follicle in vitro Xu, Gaixia Lin, Suxia Law, Wing-Cheung Roy, Indrajit Lin, Xiaotan Mei, Shujiang Ma, Hanwu Chen, Siping Niu, Hanben Wang, Xiaomei Theranostics Research Paper The toxicity of QD has been extensively studied over the past decade. However, the potential toxicity of QDs impedes its use for clinical research. In this work, we established a preantral follicle in vitro culture system to investigate the effects of QD-Transferrin (QDs-Tf) bioconjugates on follicle development and oocyte maturation. The preantral follicles were cultured and exposed to CdTe/ZnTe QDs-Tf bioconjugates with various concentrations and the reproductive toxicity was assessed at different time points post-treatment. The invasion of QDs-Tf for oocytes was verified by laser scanning confocal microscope. Steroid production was evaluated by immunoassay. C-band Giemsa staining was performed to observe the chromosome abnormality of oocytes. The results showed that the QDs-Tf bioconjugates could permeate into granulosa cells and theca cells, but not into oocyte. There are no obvious changes of oocyte diameter, the mucification of cumulus-oocyte-complexes and the occurrence of aneulpoidy as compared with the control group. However, delay in the antrum formation and decrease in the ratio of oocytes with first polar body were observed in QDs-Tf-treated groups. The matured oocytes with first polar body decreased significantly by ~16% (from 79.6±10 % to 63±2.9 %) when the concentration of QDs-Tf bioconjugates exceeded 2.89 nmol·L(-1) (P < 0.05). Our results implied that the CdTe/ZnTe QDs-Tf bioconjugates were reproductive toxic for follicle development, and thus also revealed that this in vitro culture system of preantral follicle is a highly sensitive tool for study on the reproductive toxicity of nanoparticles. Ivyspring International Publisher 2012-08-01 /pmc/articles/PMC3425092/ /pubmed/22916073 http://dx.doi.org/10.7150/thno.4290 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Research Paper
Xu, Gaixia
Lin, Suxia
Law, Wing-Cheung
Roy, Indrajit
Lin, Xiaotan
Mei, Shujiang
Ma, Hanwu
Chen, Siping
Niu, Hanben
Wang, Xiaomei
The Invasion and Reproductive Toxicity of QDs-Transferrin Bioconjugates on Preantral Follicle in vitro
title The Invasion and Reproductive Toxicity of QDs-Transferrin Bioconjugates on Preantral Follicle in vitro
title_full The Invasion and Reproductive Toxicity of QDs-Transferrin Bioconjugates on Preantral Follicle in vitro
title_fullStr The Invasion and Reproductive Toxicity of QDs-Transferrin Bioconjugates on Preantral Follicle in vitro
title_full_unstemmed The Invasion and Reproductive Toxicity of QDs-Transferrin Bioconjugates on Preantral Follicle in vitro
title_short The Invasion and Reproductive Toxicity of QDs-Transferrin Bioconjugates on Preantral Follicle in vitro
title_sort invasion and reproductive toxicity of qds-transferrin bioconjugates on preantral follicle in vitro
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425092/
https://www.ncbi.nlm.nih.gov/pubmed/22916073
http://dx.doi.org/10.7150/thno.4290
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