Chemically induced enucleation of activated bovine oocytes: chromatin and microtubule organization and production of viable cytoplasts

Detalhes bibliográficos
Autor(a) principal: Saraiva, Naiara Zoccal
Data de Publicação: 2015
Outros Autores: Oliveira, Clara Slade, Verde Leal, Claudia Lima, Lima, Marina Ragagnin de, Del Collado, Maite, Vantini, Roberta, Monteiro, Fabio Morato, Meo Niciura, Simone Cristina, Garcia, Joaquim Mansano
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1017/S0967199414000537
http://hdl.handle.net/11449/158586
Resumo: As the standard enucleation method in mammalian nuclear transfer is invasive and damaging to cytoplast spatial organization, alternative procedures have been developed over recent years. Among these techniques, chemically induced enucleation (IE) is especially interesting because it does not employ ultraviolet light and reduces the amount of cytoplasm eliminated during the procedure. The objective of this study was to optimize the culture conditions with demecolcine of pre-activated bovine oocytes for chemically IE, and to evaluate nuclear and microtubule organization in cytoplasts obtained by this technique and their viability. In the first experiment, a negative effect on oocyte activation was verified when demecolcine was added at the beginning of the process, reducing activation rates by approximately 30%. This effect was not observed when demecolcine was added to the medium after 1.5 h of activation. In the second experiment, although a reduction in the number of microtubules was observed in most oocytes, these structures did not disappear completely during assessment. Approximately 50% of treated oocytes presented microtubule reduction at the end of the evaluation period, while 23% of oocytes were observed to exhibit the complete disappearance of these structures and 28% exhibited visible microtubules. These findings indicated the lack of immediate microtubule repolymerization after culture in demecolcine-free medium, a fact that may negatively influence embryonic development. However, cleavage rates of 63.6-70.0% and blastocyst yield of 15.5-24.2% were obtained in the final experiment, without significant differences between techniques, indicating that chemically induced enucleation produces normal embryos.
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spelling Chemically induced enucleation of activated bovine oocytes: chromatin and microtubule organization and production of viable cytoplastsBovineChemically induced enucleationChromatinMicrotubuleNuclear transferAs the standard enucleation method in mammalian nuclear transfer is invasive and damaging to cytoplast spatial organization, alternative procedures have been developed over recent years. Among these techniques, chemically induced enucleation (IE) is especially interesting because it does not employ ultraviolet light and reduces the amount of cytoplasm eliminated during the procedure. The objective of this study was to optimize the culture conditions with demecolcine of pre-activated bovine oocytes for chemically IE, and to evaluate nuclear and microtubule organization in cytoplasts obtained by this technique and their viability. In the first experiment, a negative effect on oocyte activation was verified when demecolcine was added at the beginning of the process, reducing activation rates by approximately 30%. This effect was not observed when demecolcine was added to the medium after 1.5 h of activation. In the second experiment, although a reduction in the number of microtubules was observed in most oocytes, these structures did not disappear completely during assessment. Approximately 50% of treated oocytes presented microtubule reduction at the end of the evaluation period, while 23% of oocytes were observed to exhibit the complete disappearance of these structures and 28% exhibited visible microtubules. These findings indicated the lack of immediate microtubule repolymerization after culture in demecolcine-free medium, a fact that may negatively influence embryonic development. However, cleavage rates of 63.6-70.0% and blastocyst yield of 15.5-24.2% were obtained in the final experiment, without significant differences between techniques, indicating that chemically induced enucleation produces normal embryos.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Embrapa Amazonia Oriental, BR-66095100 Belem, Para, BrazilUniv Estadual Paulista, Jaboticabal, BrazilEmbrapa Dairy Cattle, Valenca, BrazilUniv Sao Paulo, Fac Zootecnia & Engn Alimentos, Pirassununga, BrazilInst Zootecnia, Sertaozinho, BrazilEmbrapa Southeast Livestock, Sao Carlos, SP, BrazilUniv Estadual Paulista, Jaboticabal, BrazilCambridge Univ PressEmpresa Brasileira de Pesquisa Agropecuária (EMBRAPA)Universidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Inst ZootecniaSaraiva, Naiara ZoccalOliveira, Clara SladeVerde Leal, Claudia LimaLima, Marina Ragagnin deDel Collado, MaiteVantini, RobertaMonteiro, Fabio MoratoMeo Niciura, Simone CristinaGarcia, Joaquim Mansano2018-11-26T15:28:12Z2018-11-26T15:28:12Z2015-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article852-862application/pdfhttp://dx.doi.org/10.1017/S0967199414000537Zygote. New York: Cambridge Univ Press, v. 23, n. 6, p. 852-862, 2015.0967-1994http://hdl.handle.net/11449/15858610.1017/S0967199414000537WOS:000364956200007WOS000364956200007.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengZygote0,387info:eu-repo/semantics/openAccess2023-10-09T06:06:28Zoai:repositorio.unesp.br:11449/158586Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:27:34.441464Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Chemically induced enucleation of activated bovine oocytes: chromatin and microtubule organization and production of viable cytoplasts
title Chemically induced enucleation of activated bovine oocytes: chromatin and microtubule organization and production of viable cytoplasts
spellingShingle Chemically induced enucleation of activated bovine oocytes: chromatin and microtubule organization and production of viable cytoplasts
Saraiva, Naiara Zoccal
Bovine
Chemically induced enucleation
Chromatin
Microtubule
Nuclear transfer
title_short Chemically induced enucleation of activated bovine oocytes: chromatin and microtubule organization and production of viable cytoplasts
title_full Chemically induced enucleation of activated bovine oocytes: chromatin and microtubule organization and production of viable cytoplasts
title_fullStr Chemically induced enucleation of activated bovine oocytes: chromatin and microtubule organization and production of viable cytoplasts
title_full_unstemmed Chemically induced enucleation of activated bovine oocytes: chromatin and microtubule organization and production of viable cytoplasts
title_sort Chemically induced enucleation of activated bovine oocytes: chromatin and microtubule organization and production of viable cytoplasts
author Saraiva, Naiara Zoccal
author_facet Saraiva, Naiara Zoccal
Oliveira, Clara Slade
Verde Leal, Claudia Lima
Lima, Marina Ragagnin de
Del Collado, Maite
Vantini, Roberta
Monteiro, Fabio Morato
Meo Niciura, Simone Cristina
Garcia, Joaquim Mansano
author_role author
author2 Oliveira, Clara Slade
Verde Leal, Claudia Lima
Lima, Marina Ragagnin de
Del Collado, Maite
Vantini, Roberta
Monteiro, Fabio Morato
Meo Niciura, Simone Cristina
Garcia, Joaquim Mansano
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Empresa Brasileira de Pesquisa Agropecuária (EMBRAPA)
Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
Inst Zootecnia
dc.contributor.author.fl_str_mv Saraiva, Naiara Zoccal
Oliveira, Clara Slade
Verde Leal, Claudia Lima
Lima, Marina Ragagnin de
Del Collado, Maite
Vantini, Roberta
Monteiro, Fabio Morato
Meo Niciura, Simone Cristina
Garcia, Joaquim Mansano
dc.subject.por.fl_str_mv Bovine
Chemically induced enucleation
Chromatin
Microtubule
Nuclear transfer
topic Bovine
Chemically induced enucleation
Chromatin
Microtubule
Nuclear transfer
description As the standard enucleation method in mammalian nuclear transfer is invasive and damaging to cytoplast spatial organization, alternative procedures have been developed over recent years. Among these techniques, chemically induced enucleation (IE) is especially interesting because it does not employ ultraviolet light and reduces the amount of cytoplasm eliminated during the procedure. The objective of this study was to optimize the culture conditions with demecolcine of pre-activated bovine oocytes for chemically IE, and to evaluate nuclear and microtubule organization in cytoplasts obtained by this technique and their viability. In the first experiment, a negative effect on oocyte activation was verified when demecolcine was added at the beginning of the process, reducing activation rates by approximately 30%. This effect was not observed when demecolcine was added to the medium after 1.5 h of activation. In the second experiment, although a reduction in the number of microtubules was observed in most oocytes, these structures did not disappear completely during assessment. Approximately 50% of treated oocytes presented microtubule reduction at the end of the evaluation period, while 23% of oocytes were observed to exhibit the complete disappearance of these structures and 28% exhibited visible microtubules. These findings indicated the lack of immediate microtubule repolymerization after culture in demecolcine-free medium, a fact that may negatively influence embryonic development. However, cleavage rates of 63.6-70.0% and blastocyst yield of 15.5-24.2% were obtained in the final experiment, without significant differences between techniques, indicating that chemically induced enucleation produces normal embryos.
publishDate 2015
dc.date.none.fl_str_mv 2015-12-01
2018-11-26T15:28:12Z
2018-11-26T15:28:12Z
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/10.1017/S0967199414000537
Zygote. New York: Cambridge Univ Press, v. 23, n. 6, p. 852-862, 2015.
0967-1994
http://hdl.handle.net/11449/158586
10.1017/S0967199414000537
WOS:000364956200007
WOS000364956200007.pdf
url http://dx.doi.org/10.1017/S0967199414000537
http://hdl.handle.net/11449/158586
identifier_str_mv Zygote. New York: Cambridge Univ Press, v. 23, n. 6, p. 852-862, 2015.
0967-1994
10.1017/S0967199414000537
WOS:000364956200007
WOS000364956200007.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Zygote
0,387
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 852-862
application/pdf
dc.publisher.none.fl_str_mv Cambridge Univ Press
publisher.none.fl_str_mv Cambridge Univ Press
dc.source.none.fl_str_mv Web of Science
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
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