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Vitrification freezing of large ovarian tissue in the human body
BACKGROUND: This study aims to carry out the vitrification freezing of a large ovarian tissue in the human body, and evaluate its feasibility. RESULTS: A total of 18 ovarian tissues in the human body were selected, and each tissue was cut into three large ovarian cortex slices. These tissues were ra...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706921/ https://www.ncbi.nlm.nih.gov/pubmed/31438999 http://dx.doi.org/10.1186/s13048-019-0553-x |
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author | Zhao, Qian Zhang, Ying Su, Ke Wang, Xiao-Wan Hai, Pan-Pan Han, Bing Bian, Ai-Ping Guo, Rui-Xia |
author_facet | Zhao, Qian Zhang, Ying Su, Ke Wang, Xiao-Wan Hai, Pan-Pan Han, Bing Bian, Ai-Ping Guo, Rui-Xia |
author_sort | Zhao, Qian |
collection | PubMed |
description | BACKGROUND: This study aims to carry out the vitrification freezing of a large ovarian tissue in the human body, and evaluate its feasibility. RESULTS: A total of 18 ovarian tissues in the human body were selected, and each tissue was cut into three large ovarian cortex slices. These tissues were randomly divided into three groups: vitrification freezing group (group A), programmed freezing group (group B), and fresh control group (group C). Then, the morphological analysis and apoptosis detection of each ovarian tissue was carried out, followed by the recycling of ovarian tissues at three weeks after the heterotransplantation of nude mice, in order to detect the follicle preservation conditions. The immunohistochemistory method was applied to detect the follicle activity. In comparing the proportion of primordial follicle with normal morphology after unfreezing between group A and group B, the difference was not statistically significant (P > 0.05). Furthermore, the incidence of follicle apoptosis in group A and group B was higher than that in the group C (P < 0.05). However, when comparing between group A and group B, the difference was not statistically significant (P > 0.05). The interstitial cell apoptosis rate in group A was lower than that of the group B, showing that the difference was statistically significant (P < 0.05). CONCLUSIONS: Compared with programmed freezing, the vitrification freezing of large ovarian tissues in the human body was feasible to a certain extent. This can be used as an alternative scheme to realize the freeze preservation of ovarian tissues in the human body. |
format | Online Article Text |
id | pubmed-6706921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67069212019-08-28 Vitrification freezing of large ovarian tissue in the human body Zhao, Qian Zhang, Ying Su, Ke Wang, Xiao-Wan Hai, Pan-Pan Han, Bing Bian, Ai-Ping Guo, Rui-Xia J Ovarian Res Research BACKGROUND: This study aims to carry out the vitrification freezing of a large ovarian tissue in the human body, and evaluate its feasibility. RESULTS: A total of 18 ovarian tissues in the human body were selected, and each tissue was cut into three large ovarian cortex slices. These tissues were randomly divided into three groups: vitrification freezing group (group A), programmed freezing group (group B), and fresh control group (group C). Then, the morphological analysis and apoptosis detection of each ovarian tissue was carried out, followed by the recycling of ovarian tissues at three weeks after the heterotransplantation of nude mice, in order to detect the follicle preservation conditions. The immunohistochemistory method was applied to detect the follicle activity. In comparing the proportion of primordial follicle with normal morphology after unfreezing between group A and group B, the difference was not statistically significant (P > 0.05). Furthermore, the incidence of follicle apoptosis in group A and group B was higher than that in the group C (P < 0.05). However, when comparing between group A and group B, the difference was not statistically significant (P > 0.05). The interstitial cell apoptosis rate in group A was lower than that of the group B, showing that the difference was statistically significant (P < 0.05). CONCLUSIONS: Compared with programmed freezing, the vitrification freezing of large ovarian tissues in the human body was feasible to a certain extent. This can be used as an alternative scheme to realize the freeze preservation of ovarian tissues in the human body. BioMed Central 2019-08-22 /pmc/articles/PMC6706921/ /pubmed/31438999 http://dx.doi.org/10.1186/s13048-019-0553-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Zhao, Qian Zhang, Ying Su, Ke Wang, Xiao-Wan Hai, Pan-Pan Han, Bing Bian, Ai-Ping Guo, Rui-Xia Vitrification freezing of large ovarian tissue in the human body |
title | Vitrification freezing of large ovarian tissue in the human body |
title_full | Vitrification freezing of large ovarian tissue in the human body |
title_fullStr | Vitrification freezing of large ovarian tissue in the human body |
title_full_unstemmed | Vitrification freezing of large ovarian tissue in the human body |
title_short | Vitrification freezing of large ovarian tissue in the human body |
title_sort | vitrification freezing of large ovarian tissue in the human body |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706921/ https://www.ncbi.nlm.nih.gov/pubmed/31438999 http://dx.doi.org/10.1186/s13048-019-0553-x |
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