Characterization and enrichment of spermatogonial stem cells of common carp (Cyprinus carpio)

Bibliographic Details
Main Author: Vigoya, Angel A.A. [UNESP]
Publication Date: 2024
Other Authors: Martinez, Emanuel R.M. [UNESP], Digmayer, Melanie [UNESP], de Oliveira, Marcos A. [UNESP], Butzge, Arno J. [UNESP], Rosa, Ivana F. [UNESP], Doretto, Lucas B. [UNESP], Nóbrega, Rafael H. [UNESP]
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1016/j.theriogenology.2023.10.021
https://hdl.handle.net/11449/300601
Summary: Spermatogenesis is a systematically organized process that ensures uninterrupted sperm production in which the spermatogonial stem cells (SSCs) play a crucial role. However, the existing absence of teleost-specific molecular markers for SSCs presents a notable challenge. Herein we characterized phenotypically the spermatogonial stem cells using specific molecular markers and transmission electron microscopy. Moreover, we also describe a simple method to suppress common carp spermatogenesis using the combination of Busulfan and thermo-chemical treatment, and finally, we isolate and enrich the undifferentiated spermatogonial fraction. Our results showed that C-kit, GFRα1, and POU2 proteins were expressed by germ cells, meanwhile, undifferentiated spermatogonial populations preferentially expressed GFRα1 and POU2. Moreover, the combination of high temperature (35 °C) and Busulfan (40 mg/kg/BW) effectively suppressed the spermatogenesis of common carp males. Additionally, the amh expression analysis showed differences between the control (26 °C) when compared to 35 °C with a single or two Busulfan doses, confirming that the testes were depleted by the association of Busulfan at high temperatures. In an attempt to isolate the undifferentiated spermatogonial fraction, we used the Percoll discontinuous density gradient. Thus, we successfully dissociated the carp whole testes in different cellular fractions; subsequently, we isolated and enriched the undifferentiated spermatogonial population. Therefore, our results suggest that probably both GFRα-1 and POU2 are highly conserved factors expressed in common carp germinative epithelium and that these molecules were well conserved along the evolutionary process. Furthermore, the enriched undifferentiated spermatogonial population developed here can be used in further germ cell transplantation experiments to preserve and propagate valued and endangered fish species.
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spelling Characterization and enrichment of spermatogonial stem cells of common carp (Cyprinus carpio)Common carp (Cyprinus carpio)GFRα-1Percoll gradientPOU2Spermatogenesis depletionSpermatogonia stem cell enrichmentStem cell markersSpermatogenesis is a systematically organized process that ensures uninterrupted sperm production in which the spermatogonial stem cells (SSCs) play a crucial role. However, the existing absence of teleost-specific molecular markers for SSCs presents a notable challenge. Herein we characterized phenotypically the spermatogonial stem cells using specific molecular markers and transmission electron microscopy. Moreover, we also describe a simple method to suppress common carp spermatogenesis using the combination of Busulfan and thermo-chemical treatment, and finally, we isolate and enrich the undifferentiated spermatogonial fraction. Our results showed that C-kit, GFRα1, and POU2 proteins were expressed by germ cells, meanwhile, undifferentiated spermatogonial populations preferentially expressed GFRα1 and POU2. Moreover, the combination of high temperature (35 °C) and Busulfan (40 mg/kg/BW) effectively suppressed the spermatogenesis of common carp males. Additionally, the amh expression analysis showed differences between the control (26 °C) when compared to 35 °C with a single or two Busulfan doses, confirming that the testes were depleted by the association of Busulfan at high temperatures. In an attempt to isolate the undifferentiated spermatogonial fraction, we used the Percoll discontinuous density gradient. Thus, we successfully dissociated the carp whole testes in different cellular fractions; subsequently, we isolated and enriched the undifferentiated spermatogonial population. Therefore, our results suggest that probably both GFRα-1 and POU2 are highly conserved factors expressed in common carp germinative epithelium and that these molecules were well conserved along the evolutionary process. Furthermore, the enriched undifferentiated spermatogonial population developed here can be used in further germ cell transplantation experiments to preserve and propagate valued and endangered fish species.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Aquaculture Center of São Paulo State University CAUNESP, JaboticabalFaculty of Veterinary Medicine and Animal Science San Martín University Foundation (FUSM)Department of Structural and Functional Biology Institute of Biosciences São Paulo State University (UNESP)Yellow Sea Fisheries Research Institute Chinese Academy of Fishery SciencesNational Key Laboratory of Mariculture Biobreeding and Sustainable GoodsAquaculture Center of São Paulo State University CAUNESP, JaboticabalDepartment of Structural and Functional Biology Institute of Biosciences São Paulo State University (UNESP)FAPESP: 14/07620-7Universidade Estadual Paulista (UNESP)San Martín University Foundation (FUSM)Chinese Academy of Fishery SciencesNational Key Laboratory of Mariculture Biobreeding and Sustainable GoodsVigoya, Angel A.A. [UNESP]Martinez, Emanuel R.M. [UNESP]Digmayer, Melanie [UNESP]de Oliveira, Marcos A. [UNESP]Butzge, Arno J. [UNESP]Rosa, Ivana F. [UNESP]Doretto, Lucas B. [UNESP]Nóbrega, Rafael H. [UNESP]2025-04-29T18:50:04Z2024-01-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article233-244http://dx.doi.org/10.1016/j.theriogenology.2023.10.021Theriogenology, v. 214, p. 233-244.0093-691Xhttps://hdl.handle.net/11449/30060110.1016/j.theriogenology.2023.10.0212-s2.0-85175863133Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengTheriogenologyinfo:eu-repo/semantics/openAccess2025-04-30T13:37:31Zoai:repositorio.unesp.br:11449/300601Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-04-30T13:37:31Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Characterization and enrichment of spermatogonial stem cells of common carp (Cyprinus carpio)
title Characterization and enrichment of spermatogonial stem cells of common carp (Cyprinus carpio)
spellingShingle Characterization and enrichment of spermatogonial stem cells of common carp (Cyprinus carpio)
Vigoya, Angel A.A. [UNESP]
Common carp (Cyprinus carpio)
GFRα-1
Percoll gradient
POU2
Spermatogenesis depletion
Spermatogonia stem cell enrichment
Stem cell markers
title_short Characterization and enrichment of spermatogonial stem cells of common carp (Cyprinus carpio)
title_full Characterization and enrichment of spermatogonial stem cells of common carp (Cyprinus carpio)
title_fullStr Characterization and enrichment of spermatogonial stem cells of common carp (Cyprinus carpio)
title_full_unstemmed Characterization and enrichment of spermatogonial stem cells of common carp (Cyprinus carpio)
title_sort Characterization and enrichment of spermatogonial stem cells of common carp (Cyprinus carpio)
author Vigoya, Angel A.A. [UNESP]
author_facet Vigoya, Angel A.A. [UNESP]
Martinez, Emanuel R.M. [UNESP]
Digmayer, Melanie [UNESP]
de Oliveira, Marcos A. [UNESP]
Butzge, Arno J. [UNESP]
Rosa, Ivana F. [UNESP]
Doretto, Lucas B. [UNESP]
Nóbrega, Rafael H. [UNESP]
author_role author
author2 Martinez, Emanuel R.M. [UNESP]
Digmayer, Melanie [UNESP]
de Oliveira, Marcos A. [UNESP]
Butzge, Arno J. [UNESP]
Rosa, Ivana F. [UNESP]
Doretto, Lucas B. [UNESP]
Nóbrega, Rafael H. [UNESP]
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
San Martín University Foundation (FUSM)
Chinese Academy of Fishery Sciences
National Key Laboratory of Mariculture Biobreeding and Sustainable Goods
dc.contributor.author.fl_str_mv Vigoya, Angel A.A. [UNESP]
Martinez, Emanuel R.M. [UNESP]
Digmayer, Melanie [UNESP]
de Oliveira, Marcos A. [UNESP]
Butzge, Arno J. [UNESP]
Rosa, Ivana F. [UNESP]
Doretto, Lucas B. [UNESP]
Nóbrega, Rafael H. [UNESP]
dc.subject.por.fl_str_mv Common carp (Cyprinus carpio)
GFRα-1
Percoll gradient
POU2
Spermatogenesis depletion
Spermatogonia stem cell enrichment
Stem cell markers
topic Common carp (Cyprinus carpio)
GFRα-1
Percoll gradient
POU2
Spermatogenesis depletion
Spermatogonia stem cell enrichment
Stem cell markers
description Spermatogenesis is a systematically organized process that ensures uninterrupted sperm production in which the spermatogonial stem cells (SSCs) play a crucial role. However, the existing absence of teleost-specific molecular markers for SSCs presents a notable challenge. Herein we characterized phenotypically the spermatogonial stem cells using specific molecular markers and transmission electron microscopy. Moreover, we also describe a simple method to suppress common carp spermatogenesis using the combination of Busulfan and thermo-chemical treatment, and finally, we isolate and enrich the undifferentiated spermatogonial fraction. Our results showed that C-kit, GFRα1, and POU2 proteins were expressed by germ cells, meanwhile, undifferentiated spermatogonial populations preferentially expressed GFRα1 and POU2. Moreover, the combination of high temperature (35 °C) and Busulfan (40 mg/kg/BW) effectively suppressed the spermatogenesis of common carp males. Additionally, the amh expression analysis showed differences between the control (26 °C) when compared to 35 °C with a single or two Busulfan doses, confirming that the testes were depleted by the association of Busulfan at high temperatures. In an attempt to isolate the undifferentiated spermatogonial fraction, we used the Percoll discontinuous density gradient. Thus, we successfully dissociated the carp whole testes in different cellular fractions; subsequently, we isolated and enriched the undifferentiated spermatogonial population. Therefore, our results suggest that probably both GFRα-1 and POU2 are highly conserved factors expressed in common carp germinative epithelium and that these molecules were well conserved along the evolutionary process. Furthermore, the enriched undifferentiated spermatogonial population developed here can be used in further germ cell transplantation experiments to preserve and propagate valued and endangered fish species.
publishDate 2024
dc.date.none.fl_str_mv 2024-01-15
2025-04-29T18:50:04Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.theriogenology.2023.10.021
Theriogenology, v. 214, p. 233-244.
0093-691X
https://hdl.handle.net/11449/300601
10.1016/j.theriogenology.2023.10.021
2-s2.0-85175863133
url http://dx.doi.org/10.1016/j.theriogenology.2023.10.021
https://hdl.handle.net/11449/300601
identifier_str_mv Theriogenology, v. 214, p. 233-244.
0093-691X
10.1016/j.theriogenology.2023.10.021
2-s2.0-85175863133
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Theriogenology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 233-244
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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