Chemically induced enucleation of activated bovine oocytes: chromatin and microtubule organization and production of viable cytoplasts
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , , , , |
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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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 |
|
_version_ |
1808128362669932544 |