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Morphologic, viability and ultrastructural analysis of vitrified sheep preantral follicles enclosed in ovarian tissue

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Main Author: Lunardi, Franciele Osmarini
Publication Date: 2012
Other Authors: Araújo, Valdevane Rocha, Faustino, Luciana Rocha, Carvalho, Adeline de Andrade, Gonçalves, Raphael Fernando Braga, Bassa, Casie Shantel, Báo, Sônia Nair, Name, Khesller Patrícia Olázia, Campello, Claudio Cabral, Figueiredo, José Ricardo de, Rodrigues, Ana Paula Ribeiro
Format: Article
Language: eng
Source: Repositório Institucional da UnB
Download full: http://repositorio.unb.br/handle/10482/17635
Summary: The main objective was to compare the efficiency of vitrification techniques and solutions on the preservation of morphology, ultrastructure and viability of sheep preantral follicles enclosed in ovarian tissue fragments. The fragments were cryopreserved by using macrotube vitrification (MTV), solid-surface vitrification (SSV) or conventional vitrification (CV). These techniques were combined with one of the six solutions containing 6 M ethylene glycol (EG) and with or without sucrose (SUC) (0.25 or 0.50 M) and with or without fetal calf serum (FCS) (10%). After one week, samples were warmed and histological analysis was performed, showing that the percentage of normal follicles after CV (66.20 ± 8.87%) using a solution containing 6 M EG, 0.25 M SUC and 10% FCS (vitrification solution 4 – VS4) was similar to fresh control (79.40 ± 7.83%), MTV (53.40 ± 10.60%) and SSV (56.75 ± 15.33%), all of them with the same vitrification solution (P < 0.05). For follicular viability evaluation, ovarian fragments were vitrified as described above. After warming, follicles were assessed by trypan blue dye. Controversially, the highest percentage of viable follicles was observed in MTV (97.06%) and was similar to fresh control (92.62%) (P < 0.05), but was significantly different from SSV (81.08%) and CV (83.81%) (P < 0.05). These results were validated by transmission electron microscopy that showed normal follicles observed in MTV and in fresh control. In addition, to verify the MTV with VS4 (a combination of the best technique plus the best solution), follicle viability was evaluated after 48 h in vitro culture. The viability assay was performed by fluorescence microscopy (calcein-AM and ethidium homodimer-1) analysis as follows: follicles isolated from fresh tissue were forthwith analyzed or underwent 48 h in vitro culture before analysis, whereas others fragments were vitrified/warmed and immediately analyzed or underwent 48 h in vitro culture before analysis. These results showed that, although follicular viability after MTV/VS4 (65%) was reduced when compared to the non-vitrified follicles at day 0 (100%), follicular viability after MTV/VS4 at day 2 (36.5%) was similar to follicles vitrified at day 0 (65%) and similar to non-vitrified follicles at day 2 (62.5%) (P > 0.05). As the decrease of viability in non-vitrified follicles at day 2 was similar to the decrease of MTV/VS4 in the same time, follicle viability at day 2 is not affected by MTV/VS4. In conclusion, using the experimental conditions of the present study, an efficient solution (VS4: 6 M EG, 0.25 M SUC and 10% FCS) and technique (MTV) were successfully used to vitrify ovine ovarian tissue.
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author Lunardi, Franciele Osmarini
author2 Araújo, Valdevane Rocha
Faustino, Luciana Rocha
Carvalho, Adeline de Andrade
Gonçalves, Raphael Fernando Braga
Bassa, Casie Shantel
Báo, Sônia Nair
Name, Khesller Patrícia Olázia
Campello, Claudio Cabral
Figueiredo, José Ricardo de
Rodrigues, Ana Paula Ribeiro
author2_role author
author
author
author
author
author
author
author
author
author
author_browse Araújo, Valdevane Rocha
Bassa, Casie Shantel
Báo, Sônia Nair
Campello, Claudio Cabral
Carvalho, Adeline de Andrade
Faustino, Luciana Rocha
Figueiredo, José Ricardo de
Gonçalves, Raphael Fernando Braga
Lunardi, Franciele Osmarini
Name, Khesller Patrícia Olázia
Rodrigues, Ana Paula Ribeiro
author_facet Lunardi, Franciele Osmarini
Araújo, Valdevane Rocha
Faustino, Luciana Rocha
Carvalho, Adeline de Andrade
Gonçalves, Raphael Fernando Braga
Bassa, Casie Shantel
Báo, Sônia Nair
Name, Khesller Patrícia Olázia
Campello, Claudio Cabral
Figueiredo, José Ricardo de
Rodrigues, Ana Paula Ribeiro
author_role author
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collection Repositório Institucional da UnB
dc.contributor.author.fl_str_mv Lunardi, Franciele Osmarini
Araújo, Valdevane Rocha
Faustino, Luciana Rocha
Carvalho, Adeline de Andrade
Gonçalves, Raphael Fernando Braga
Bassa, Casie Shantel
Báo, Sônia Nair
Name, Khesller Patrícia Olázia
Campello, Claudio Cabral
Figueiredo, José Ricardo de
Rodrigues, Ana Paula Ribeiro
dc.date.accessioned.fl_str_mv 2015-02-11T12:26:43Z
dc.date.available.fl_str_mv 2015-02-11T12:26:43Z
dc.date.issued.fl_str_mv 2012
dc.identifier.citation.fl_str_mv LUNARDI, Franciele Osmarini, et al. Morphologic, viability and ultrastructural analysis of vitrified sheep preantral follicles enclosed in ovarian tissue. Small Ruminant Research, v. 107, p. 121-130, 2012. Disponível em:<http://www.sciencedirect.com/science/article/pii/S0921448812001599>. Acesso em: 03 fev. 2015.
dc.identifier.uri.fl_str_mv http://repositorio.unb.br/handle/10482/17635
dc.language.iso.fl_str_mv eng
dc.publisher.none.fl_str_mv Elsevier
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
dc.source.none.fl_str_mv reponame:Repositório Institucional da UnB
instname:Universidade de Brasília (UnB)
instacron:UNB
dc.subject.keyword.en.fl_str_mv Ovelha
Ovários
Criopreservação de órgãos, tecidos, etc.
Folículos pré-antrais
dc.title.en.fl_str_mv Morphologic, viability and ultrastructural analysis of vitrified sheep preantral follicles enclosed in ovarian tissue
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
description The main objective was to compare the efficiency of vitrification techniques and solutions on the preservation of morphology, ultrastructure and viability of sheep preantral follicles enclosed in ovarian tissue fragments. The fragments were cryopreserved by using macrotube vitrification (MTV), solid-surface vitrification (SSV) or conventional vitrification (CV). These techniques were combined with one of the six solutions containing 6 M ethylene glycol (EG) and with or without sucrose (SUC) (0.25 or 0.50 M) and with or without fetal calf serum (FCS) (10%). After one week, samples were warmed and histological analysis was performed, showing that the percentage of normal follicles after CV (66.20 ± 8.87%) using a solution containing 6 M EG, 0.25 M SUC and 10% FCS (vitrification solution 4 – VS4) was similar to fresh control (79.40 ± 7.83%), MTV (53.40 ± 10.60%) and SSV (56.75 ± 15.33%), all of them with the same vitrification solution (P < 0.05). For follicular viability evaluation, ovarian fragments were vitrified as described above. After warming, follicles were assessed by trypan blue dye. Controversially, the highest percentage of viable follicles was observed in MTV (97.06%) and was similar to fresh control (92.62%) (P < 0.05), but was significantly different from SSV (81.08%) and CV (83.81%) (P < 0.05). These results were validated by transmission electron microscopy that showed normal follicles observed in MTV and in fresh control. In addition, to verify the MTV with VS4 (a combination of the best technique plus the best solution), follicle viability was evaluated after 48 h in vitro culture. The viability assay was performed by fluorescence microscopy (calcein-AM and ethidium homodimer-1) analysis as follows: follicles isolated from fresh tissue were forthwith analyzed or underwent 48 h in vitro culture before analysis, whereas others fragments were vitrified/warmed and immediately analyzed or underwent 48 h in vitro culture before analysis. These results showed that, although follicular viability after MTV/VS4 (65%) was reduced when compared to the non-vitrified follicles at day 0 (100%), follicular viability after MTV/VS4 at day 2 (36.5%) was similar to follicles vitrified at day 0 (65%) and similar to non-vitrified follicles at day 2 (62.5%) (P > 0.05). As the decrease of viability in non-vitrified follicles at day 2 was similar to the decrease of MTV/VS4 in the same time, follicle viability at day 2 is not affected by MTV/VS4. In conclusion, using the experimental conditions of the present study, an efficient solution (VS4: 6 M EG, 0.25 M SUC and 10% FCS) and technique (MTV) were successfully used to vitrify ovine ovarian tissue.
eu_rights_str_mv openAccess
format article
id UNB_dabdb071e9cf395f3a98b1ccbf3bc9e0
identifier_str_mv LUNARDI, Franciele Osmarini, et al. Morphologic, viability and ultrastructural analysis of vitrified sheep preantral follicles enclosed in ovarian tissue. Small Ruminant Research, v. 107, p. 121-130, 2012. Disponível em:<http://www.sciencedirect.com/science/article/pii/S0921448812001599>. Acesso em: 03 fev. 2015.
instacron_str UNB
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instname_str Universidade de Brasília (UnB)
language eng
network_acronym_str UNB
network_name_str Repositório Institucional da UnB
oai_identifier_str oai:repositorio.unb.br:10482/17635
publishDate 2012
publishDateSort 2012
publisher.none.fl_str_mv Elsevier
reponame_str Repositório Institucional da UnB
repository.mail.fl_str_mv repositorio@unb.br
repository.name.fl_str_mv Repositório Institucional da UnB - Universidade de Brasília (UnB)
repository_id_str
spelling Lunardi, Franciele OsmariniAraújo, Valdevane RochaFaustino, Luciana RochaCarvalho, Adeline de AndradeGonçalves, Raphael Fernando BragaBassa, Casie ShantelBáo, Sônia NairName, Khesller Patrícia OláziaCampello, Claudio CabralFigueiredo, José Ricardo deRodrigues, Ana Paula Ribeiro2015-02-11T12:26:43Z2015-02-11T12:26:43Z2012LUNARDI, Franciele Osmarini, et al. Morphologic, viability and ultrastructural analysis of vitrified sheep preantral follicles enclosed in ovarian tissue. Small Ruminant Research, v. 107, p. 121-130, 2012. Disponível em:<http://www.sciencedirect.com/science/article/pii/S0921448812001599>. Acesso em: 03 fev. 2015.http://repositorio.unb.br/handle/10482/17635The main objective was to compare the efficiency of vitrification techniques and solutions on the preservation of morphology, ultrastructure and viability of sheep preantral follicles enclosed in ovarian tissue fragments. The fragments were cryopreserved by using macrotube vitrification (MTV), solid-surface vitrification (SSV) or conventional vitrification (CV). These techniques were combined with one of the six solutions containing 6 M ethylene glycol (EG) and with or without sucrose (SUC) (0.25 or 0.50 M) and with or without fetal calf serum (FCS) (10%). After one week, samples were warmed and histological analysis was performed, showing that the percentage of normal follicles after CV (66.20 ± 8.87%) using a solution containing 6 M EG, 0.25 M SUC and 10% FCS (vitrification solution 4 – VS4) was similar to fresh control (79.40 ± 7.83%), MTV (53.40 ± 10.60%) and SSV (56.75 ± 15.33%), all of them with the same vitrification solution (P < 0.05). For follicular viability evaluation, ovarian fragments were vitrified as described above. After warming, follicles were assessed by trypan blue dye. Controversially, the highest percentage of viable follicles was observed in MTV (97.06%) and was similar to fresh control (92.62%) (P < 0.05), but was significantly different from SSV (81.08%) and CV (83.81%) (P < 0.05). These results were validated by transmission electron microscopy that showed normal follicles observed in MTV and in fresh control. In addition, to verify the MTV with VS4 (a combination of the best technique plus the best solution), follicle viability was evaluated after 48 h in vitro culture. The viability assay was performed by fluorescence microscopy (calcein-AM and ethidium homodimer-1) analysis as follows: follicles isolated from fresh tissue were forthwith analyzed or underwent 48 h in vitro culture before analysis, whereas others fragments were vitrified/warmed and immediately analyzed or underwent 48 h in vitro culture before analysis. These results showed that, although follicular viability after MTV/VS4 (65%) was reduced when compared to the non-vitrified follicles at day 0 (100%), follicular viability after MTV/VS4 at day 2 (36.5%) was similar to follicles vitrified at day 0 (65%) and similar to non-vitrified follicles at day 2 (62.5%) (P > 0.05). As the decrease of viability in non-vitrified follicles at day 2 was similar to the decrease of MTV/VS4 in the same time, follicle viability at day 2 is not affected by MTV/VS4. In conclusion, using the experimental conditions of the present study, an efficient solution (VS4: 6 M EG, 0.25 M SUC and 10% FCS) and technique (MTV) were successfully used to vitrify ovine ovarian tissue.ElsevierEste Manuscrito do Autor Aceito para Publicação (AAM) é protegido por direitos autorais e publicado pela Elsevier. Ele esta disponível neste Repositório, por acordo entre a Elsevier e a Universidade de Brasília. As alterações decorrentes do processo de publicação - como a edição, correção, formatação estrutural, e outros mecanismos de controle de qualidade - não estão refletidas nesta versão do texto. A versão definitiva do texto foi posteriormente publicado em [Small Ruminant Research, Volume 107, Número 2-3, Outubro 2012, Pages 121–130 , doi:10.1016/j.smallrumres.2012.04.009]. Você pode baixar, copiar e utilizar de outra forma o AAM para fins não comerciais , desde que sua licença seja limitada pelas seguintes restrições: (1) Você pode usar este AAM para fins não comerciais apenas sob os termos da licença CC- BY- NC-ND. (2) A integridade do trabalho e identificação do autor, detentor dos direitos autorais e editor deve ser preservado em qualquer cópia. (3) Tem de atribuir este AAM no seguinte formato: [acordo na linguagem atribuída, incluindo o link para CC BY-NC-ND licença Digital + DOI do artigo publicado na revista Elsevier ScienceDirect ® da plataforma].info:eu-repo/semantics/openAccessMorphologic, viability and ultrastructural analysis of vitrified sheep preantral follicles enclosed in ovarian tissueinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleOvelhaOváriosCriopreservação de órgãos, tecidos, etc.Folículos pré-antraisengreponame:Repositório Institucional da UnBinstname:Universidade de Brasília (UnB)instacron:UNBORIGINALARTIGO_MorphologicViabilityUltrastructural.pdfARTIGO_MorphologicViabilityUltrastructural.pdfapplication/pdf1399435http://repositorio2.unb.br/jspui/bitstream/10482/17635/1/ARTIGO_MorphologicViabilityUltrastructural.pdfc590256940fda96133444e6b3fd7d3eeMD51open accessLICENSElicense.txtlicense.txttext/plain266http://repositorio2.unb.br/jspui/bitstream/10482/17635/2/license.txtd95c8d57a7cb3133e60bf96094a9124aMD52open access10482/176352023-05-24 20:34:27.742open accessoai:repositorio.unb.br:10482/17635TGljZW5zZSBncmFudGVkIGJ5IEFuYSBDcmlzdGluYSBCYXJib3NhIGRhIFNpbHZhIChhbm5hYmRzQGhvdG1haWwuY29tKSBvbiAyMDE1LTAyLTAzVDE1OjIwOjU3WiAoR01UKToKClN1Ym1pc3PDo28gZWZldGl2YWRhIHBvciBpbnRlZ3JhbnRlIGRhIGVxdWlwZSBkbyBSZXBvc2l0w7NyaW8gSW5zdGl0dWNpb25hbCBkYSBVbkIgZGUgYWNvcmRvIGNvbSBsaWNlbsOnYSBjb25jZWRpZGEgcGVsbyBhdXRvciBlL291IGRldGVudG9yIGRvcyBkaXJlaXRvcyBhdXRvcmFpcy4=Repositório InstitucionalPUBhttps://repositorio.unb.br/oai/requestrepositorio@unb.bropendoar:2023-05-24T23:34:27Repositório Institucional da UnB - Universidade de Brasília (UnB)
spellingShingle Morphologic, viability and ultrastructural analysis of vitrified sheep preantral follicles enclosed in ovarian tissue
Lunardi, Franciele Osmarini
Ovelha
Ovários
Criopreservação de órgãos, tecidos, etc.
Folículos pré-antrais
status_str publishedVersion
title Morphologic, viability and ultrastructural analysis of vitrified sheep preantral follicles enclosed in ovarian tissue
title_full Morphologic, viability and ultrastructural analysis of vitrified sheep preantral follicles enclosed in ovarian tissue
title_fullStr Morphologic, viability and ultrastructural analysis of vitrified sheep preantral follicles enclosed in ovarian tissue
title_full_unstemmed Morphologic, viability and ultrastructural analysis of vitrified sheep preantral follicles enclosed in ovarian tissue
title_short Morphologic, viability and ultrastructural analysis of vitrified sheep preantral follicles enclosed in ovarian tissue
title_sort Morphologic, viability and ultrastructural analysis of vitrified sheep preantral follicles enclosed in ovarian tissue
topic Ovelha
Ovários
Criopreservação de órgãos, tecidos, etc.
Folículos pré-antrais
url http://repositorio.unb.br/handle/10482/17635