Cargando…
Melatonin in cryopreservation media improves transplantation efficiency of frozen–thawed spermatogonial stem cells into testes of azoospermic mice
BACKGROUND: Cryostorage of spermatogonial stem cells (SSCs) is an appropriate procedure for long-term storage of SSCs for fertility preservation. However, it causes damage to cellular structures through overproduction of ROS and oxidative stress. In this study, we examined the protective effect of m...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327150/ https://www.ncbi.nlm.nih.gov/pubmed/35883101 http://dx.doi.org/10.1186/s13287-022-03029-1 |
_version_ | 1784757445415927808 |
---|---|
author | Kazemzadeh, Shokoofeh Mohammadpour, Shahram Madadi, Soheila Babakhani, Azar Shabani, Maryam Khanehzad, Maryam |
author_facet | Kazemzadeh, Shokoofeh Mohammadpour, Shahram Madadi, Soheila Babakhani, Azar Shabani, Maryam Khanehzad, Maryam |
author_sort | Kazemzadeh, Shokoofeh |
collection | PubMed |
description | BACKGROUND: Cryostorage of spermatogonial stem cells (SSCs) is an appropriate procedure for long-term storage of SSCs for fertility preservation. However, it causes damage to cellular structures through overproduction of ROS and oxidative stress. In this study, we examined the protective effect of melatonin as a potent antioxidant in the basic freezing medium to establish an optimal cryopreservation method for SSCs. METHODS: SSCs were obtained from the testes of neonatal male mice aged 3–6 days. Then, 100 μM melatonin was added to the basic freezing medium containing DMSO for cryopreservation of SSCs. Viability, apoptosis-related markers (BAX and BCL2), and intracellular ROS generation level were measured in frozen–thawed SSCs before transplantation using the MTT assay, immunocytochemistry, and flow cytometry, respectively. In addition, Western blotting and immunofluorescence were used to evaluate the expression of proliferation (PLZF and GFRα1) and differentiation (Stra8 and SCP3) proteins in frozen–thawed SSCs after transplantation into recipient testes. RESULTS: The data showed that adding melatonin to the cryopreservation medium markedly increased the viability and reduced intracellular ROS generation and apoptosis (by decreasing BAX and increasing BCL2) in the frozen–thawed SSCs (p < 0.05). The expression levels of proliferation (PLZF and GFRα1) and differentiation (Stra8 and SCP3) proteins and resumption of spermatogenesis from frozen–thawed SSCs followed the same pattern after transplantation. CONCLUSIONS: The results of this study revealed that adding melatonin as an antioxidant to the cryopreservation medium containing DMSO could be a promising strategy for cryopreservation of SSCs to maintain fertility in prepubertal male children who suffer from cancer. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-022-03029-1. |
format | Online Article Text |
id | pubmed-9327150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-93271502022-07-28 Melatonin in cryopreservation media improves transplantation efficiency of frozen–thawed spermatogonial stem cells into testes of azoospermic mice Kazemzadeh, Shokoofeh Mohammadpour, Shahram Madadi, Soheila Babakhani, Azar Shabani, Maryam Khanehzad, Maryam Stem Cell Res Ther Research BACKGROUND: Cryostorage of spermatogonial stem cells (SSCs) is an appropriate procedure for long-term storage of SSCs for fertility preservation. However, it causes damage to cellular structures through overproduction of ROS and oxidative stress. In this study, we examined the protective effect of melatonin as a potent antioxidant in the basic freezing medium to establish an optimal cryopreservation method for SSCs. METHODS: SSCs were obtained from the testes of neonatal male mice aged 3–6 days. Then, 100 μM melatonin was added to the basic freezing medium containing DMSO for cryopreservation of SSCs. Viability, apoptosis-related markers (BAX and BCL2), and intracellular ROS generation level were measured in frozen–thawed SSCs before transplantation using the MTT assay, immunocytochemistry, and flow cytometry, respectively. In addition, Western blotting and immunofluorescence were used to evaluate the expression of proliferation (PLZF and GFRα1) and differentiation (Stra8 and SCP3) proteins in frozen–thawed SSCs after transplantation into recipient testes. RESULTS: The data showed that adding melatonin to the cryopreservation medium markedly increased the viability and reduced intracellular ROS generation and apoptosis (by decreasing BAX and increasing BCL2) in the frozen–thawed SSCs (p < 0.05). The expression levels of proliferation (PLZF and GFRα1) and differentiation (Stra8 and SCP3) proteins and resumption of spermatogenesis from frozen–thawed SSCs followed the same pattern after transplantation. CONCLUSIONS: The results of this study revealed that adding melatonin as an antioxidant to the cryopreservation medium containing DMSO could be a promising strategy for cryopreservation of SSCs to maintain fertility in prepubertal male children who suffer from cancer. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-022-03029-1. BioMed Central 2022-07-26 /pmc/articles/PMC9327150/ /pubmed/35883101 http://dx.doi.org/10.1186/s13287-022-03029-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Kazemzadeh, Shokoofeh Mohammadpour, Shahram Madadi, Soheila Babakhani, Azar Shabani, Maryam Khanehzad, Maryam Melatonin in cryopreservation media improves transplantation efficiency of frozen–thawed spermatogonial stem cells into testes of azoospermic mice |
title | Melatonin in cryopreservation media improves transplantation efficiency of frozen–thawed spermatogonial stem cells into testes of azoospermic mice |
title_full | Melatonin in cryopreservation media improves transplantation efficiency of frozen–thawed spermatogonial stem cells into testes of azoospermic mice |
title_fullStr | Melatonin in cryopreservation media improves transplantation efficiency of frozen–thawed spermatogonial stem cells into testes of azoospermic mice |
title_full_unstemmed | Melatonin in cryopreservation media improves transplantation efficiency of frozen–thawed spermatogonial stem cells into testes of azoospermic mice |
title_short | Melatonin in cryopreservation media improves transplantation efficiency of frozen–thawed spermatogonial stem cells into testes of azoospermic mice |
title_sort | melatonin in cryopreservation media improves transplantation efficiency of frozen–thawed spermatogonial stem cells into testes of azoospermic mice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327150/ https://www.ncbi.nlm.nih.gov/pubmed/35883101 http://dx.doi.org/10.1186/s13287-022-03029-1 |
work_keys_str_mv | AT kazemzadehshokoofeh melatoninincryopreservationmediaimprovestransplantationefficiencyoffrozenthawedspermatogonialstemcellsintotestesofazoospermicmice AT mohammadpourshahram melatoninincryopreservationmediaimprovestransplantationefficiencyoffrozenthawedspermatogonialstemcellsintotestesofazoospermicmice AT madadisoheila melatoninincryopreservationmediaimprovestransplantationefficiencyoffrozenthawedspermatogonialstemcellsintotestesofazoospermicmice AT babakhaniazar melatoninincryopreservationmediaimprovestransplantationefficiencyoffrozenthawedspermatogonialstemcellsintotestesofazoospermicmice AT shabanimaryam melatoninincryopreservationmediaimprovestransplantationefficiencyoffrozenthawedspermatogonialstemcellsintotestesofazoospermicmice AT khanehzadmaryam melatoninincryopreservationmediaimprovestransplantationefficiencyoffrozenthawedspermatogonialstemcellsintotestesofazoospermicmice |