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Effect of Antifreeze Protein on Mouse Ovarian Tissue Cryopreservation and Transplantation
PURPOSE: To investigate the effect of antifreeze protein (AFP) supplementation on ovarian vitrification and transplantation. MATERIALS AND METHODS: In this experimental study, we researched a total of 182 ovaries from 4-week-old ICR mice. The equilibration solution included 20% ethylene glycol (EG),...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Yonsei University College of Medicine
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4397449/ https://www.ncbi.nlm.nih.gov/pubmed/25837185 http://dx.doi.org/10.3349/ymj.2015.56.3.778 |
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author | Lee, Jung Ryeol Youm, Hye Won Lee, Hee Jun Jee, Byung Chul Suh, Chang Suk Kim, Seok Hyun |
author_facet | Lee, Jung Ryeol Youm, Hye Won Lee, Hee Jun Jee, Byung Chul Suh, Chang Suk Kim, Seok Hyun |
author_sort | Lee, Jung Ryeol |
collection | PubMed |
description | PURPOSE: To investigate the effect of antifreeze protein (AFP) supplementation on ovarian vitrification and transplantation. MATERIALS AND METHODS: In this experimental study, we researched a total of 182 ovaries from 4-week-old ICR mice. The equilibration solution included 20% ethylene glycol (EG), and the vitrification solution included 40% EG, 18% Ficoll, and 0.3 M sucrose. Intact ovaries were first suspended in 1 mL of equilibration solution for 10 min, and then mixed with 0.5 mL of vitrification solution for 5 min. Ovaries were randomly assigned to 3 groups and 0, 5, or 20 mg/mL of type III AFP was added into the vitrification solution (control, AFP5, and AFP20 groups, respectively). The vitrified ovaries were evaluated after warming and 2 weeks after autotransplantation. The main outcome measurements are follicular morphology and apoptosis assessed by histology and the TUNEL assay. RESULTS: A significantly higher intact follicle ratio was shown in the AFP treated groups (control, 28.9%; AFP5, 42.3%; and AFP20, 44.7%). The rate of apoptotic follicles was significantly lower in the AFP treated groups (control, 26.6%; AFP5, 18.7%; and AFP20, 12.6%). After transplantation of the vitrified-warmed ovaries, a significantly higher intact follicle ratio was shown in the AFP20 group. The rate of apoptotic follicles was similar among the groups. CONCLUSION: The results of the present study suggest that supplementing AFP in the vitrification solution has beneficial effects on the survival of ovarian tissue during cryopreservation and transplantation. |
format | Online Article Text |
id | pubmed-4397449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Yonsei University College of Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-43974492015-05-01 Effect of Antifreeze Protein on Mouse Ovarian Tissue Cryopreservation and Transplantation Lee, Jung Ryeol Youm, Hye Won Lee, Hee Jun Jee, Byung Chul Suh, Chang Suk Kim, Seok Hyun Yonsei Med J Original Article PURPOSE: To investigate the effect of antifreeze protein (AFP) supplementation on ovarian vitrification and transplantation. MATERIALS AND METHODS: In this experimental study, we researched a total of 182 ovaries from 4-week-old ICR mice. The equilibration solution included 20% ethylene glycol (EG), and the vitrification solution included 40% EG, 18% Ficoll, and 0.3 M sucrose. Intact ovaries were first suspended in 1 mL of equilibration solution for 10 min, and then mixed with 0.5 mL of vitrification solution for 5 min. Ovaries were randomly assigned to 3 groups and 0, 5, or 20 mg/mL of type III AFP was added into the vitrification solution (control, AFP5, and AFP20 groups, respectively). The vitrified ovaries were evaluated after warming and 2 weeks after autotransplantation. The main outcome measurements are follicular morphology and apoptosis assessed by histology and the TUNEL assay. RESULTS: A significantly higher intact follicle ratio was shown in the AFP treated groups (control, 28.9%; AFP5, 42.3%; and AFP20, 44.7%). The rate of apoptotic follicles was significantly lower in the AFP treated groups (control, 26.6%; AFP5, 18.7%; and AFP20, 12.6%). After transplantation of the vitrified-warmed ovaries, a significantly higher intact follicle ratio was shown in the AFP20 group. The rate of apoptotic follicles was similar among the groups. CONCLUSION: The results of the present study suggest that supplementing AFP in the vitrification solution has beneficial effects on the survival of ovarian tissue during cryopreservation and transplantation. Yonsei University College of Medicine 2015-05-01 2015-04-01 /pmc/articles/PMC4397449/ /pubmed/25837185 http://dx.doi.org/10.3349/ymj.2015.56.3.778 Text en © Copyright: Yonsei University College of Medicine 2015 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Jung Ryeol Youm, Hye Won Lee, Hee Jun Jee, Byung Chul Suh, Chang Suk Kim, Seok Hyun Effect of Antifreeze Protein on Mouse Ovarian Tissue Cryopreservation and Transplantation |
title | Effect of Antifreeze Protein on Mouse Ovarian Tissue Cryopreservation and Transplantation |
title_full | Effect of Antifreeze Protein on Mouse Ovarian Tissue Cryopreservation and Transplantation |
title_fullStr | Effect of Antifreeze Protein on Mouse Ovarian Tissue Cryopreservation and Transplantation |
title_full_unstemmed | Effect of Antifreeze Protein on Mouse Ovarian Tissue Cryopreservation and Transplantation |
title_short | Effect of Antifreeze Protein on Mouse Ovarian Tissue Cryopreservation and Transplantation |
title_sort | effect of antifreeze protein on mouse ovarian tissue cryopreservation and transplantation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4397449/ https://www.ncbi.nlm.nih.gov/pubmed/25837185 http://dx.doi.org/10.3349/ymj.2015.56.3.778 |
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