Exopolysaccharide ID1 Improves Post-Warming Outcomes after Vitrification of In Vitro-Produced Bovine Embryos
This study aimed to assess the cryoprotectant role of exopolysaccharide (EPS) ID1, produced by Antarctic Pseudomonas sp., in the vitrification of in vitro-produced (IVP) bovine embryos. IVP day 7 (D7) and day 8 (D8) expanded blastocysts derived from cow or calf oocytes were vitrified without supplem...
| Autores: | , , , , , , |
|---|---|
| Formato: | artículo |
| Fecha de publicación: | 2022 |
| País: | España |
| Recursos: | Universitat Autònoma de Barcelona |
| Repositorio: | Dipòsit Digital de Documents de la UAB |
| Idioma: | inglés |
| OAI Identifier: | oai:ddd.uab.cat:260299 |
| Acesso em linha: | https://ddd.uab.cat/record/260299 https://dx.doi.org/urn:doi:10.3390/ijms23137069 |
| Access Level: | acceso abierto |
| Palavra-chave: | Cryopreservation Blastocyst Total cell number Inner cell mass TUNEL Embryo development Gene expression regulation |
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Exopolysaccharide ID1 Improves Post-Warming Outcomes after Vitrification of In Vitro-Produced Bovine EmbryosOrdóñez-León, Erika AlinaMartínez-Rodero, Iris|||0000-0001-7057-2045Garcia Martinez, Tania|||0000-0002-3428-3075López Béjar, Manel|||0000-0001-9490-6126Yeste Oliveras, Marc|||0000-0002-2209-340XMercadé, Elena|||0000-0001-7828-2210Mogas Amorós, Teresa|||0000-0002-6733-1328CryopreservationBlastocystTotal cell numberInner cell massTUNELEmbryo developmentGene expression regulationThis study aimed to assess the cryoprotectant role of exopolysaccharide (EPS) ID1, produced by Antarctic Pseudomonas sp., in the vitrification of in vitro-produced (IVP) bovine embryos. IVP day 7 (D7) and day 8 (D8) expanded blastocysts derived from cow or calf oocytes were vitrified without supplementation (EPS0) or supplemented with 10 µg/mL (EPS10) or 100 µg/mL (EPS100) EPS ID1. The effect of EPS ID1 was assessed in post-warming re-expansion and hatching rates, differential cell count, apoptosis rate, and gene expression. EPS100 re-expansion rates were significantly higher than those observed for the EPS0 and EPS10 treatments, regardless of culture length or oocyte source. EPS100 hatching rate was similar to the one of the fresh blastocysts except for those D7 blastocysts derived from calf oocytes. No differences were observed among EPS ID1 treatments when the inner cell mass, trophectoderm, and total cell number were assessed. Although apoptosis rates were higher (p ≤ 0.05) in vitrified groups compared to fresh embryos, EPS100 blastocysts had a lower number (p ≤ 0.05) of apoptotic nuclei than the EPS0 or EPS10 groups. No differences in the expression of BCL2, AQP3, CX43, and SOD1 genes between treatments were observed. Vitrification without EPS ID1 supplementation produced blastocysts with significantly higher BAX gene expression, whereas treatment with 100 µg/mL EPS ID1 returned BAX levels to those observed in non-vitrified blastocysts. Our results suggest that 100 µg/mL EPS ID1 added to the vitrification media is beneficial for embryo cryopreservation because it results in higher re-expansion and hatching ability and it positively modulates apoptosis. 22022-01-0120222022-01-01Articlehttp://purl.org/coar/resource_type/c_6501VoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleapplication/pdfhttps://ddd.uab.cat/record/260299https://dx.doi.org/urn:doi:10.3390/ijms23137069reponame:Dipòsit Digital de Documents de la UABinstname:Universitat Autònoma de BarcelonaInglésengAgencia Estatal de Investigación https://doi.org/10.13039/501100011033 PID2020-116531RB-I00Agencia Estatal de Investigación https://doi.org/10.13039/501100011033 BES-2017-081962open accesshttp://purl.org/coar/access_right/c_abf2Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original.https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessoai:ddd.uab.cat:2602992026-06-06T12:50:31Z |
| dc.title.none.fl_str_mv |
Exopolysaccharide ID1 Improves Post-Warming Outcomes after Vitrification of In Vitro-Produced Bovine Embryos |
| title |
Exopolysaccharide ID1 Improves Post-Warming Outcomes after Vitrification of In Vitro-Produced Bovine Embryos |
| spellingShingle |
Exopolysaccharide ID1 Improves Post-Warming Outcomes after Vitrification of In Vitro-Produced Bovine Embryos Ordóñez-León, Erika Alina Cryopreservation Blastocyst Total cell number Inner cell mass TUNEL Embryo development Gene expression regulation |
| title_short |
Exopolysaccharide ID1 Improves Post-Warming Outcomes after Vitrification of In Vitro-Produced Bovine Embryos |
| title_full |
Exopolysaccharide ID1 Improves Post-Warming Outcomes after Vitrification of In Vitro-Produced Bovine Embryos |
| title_fullStr |
Exopolysaccharide ID1 Improves Post-Warming Outcomes after Vitrification of In Vitro-Produced Bovine Embryos |
| title_full_unstemmed |
Exopolysaccharide ID1 Improves Post-Warming Outcomes after Vitrification of In Vitro-Produced Bovine Embryos |
| title_sort |
Exopolysaccharide ID1 Improves Post-Warming Outcomes after Vitrification of In Vitro-Produced Bovine Embryos |
| dc.creator.none.fl_str_mv |
Ordóñez-León, Erika Alina Martínez-Rodero, Iris|||0000-0001-7057-2045 Garcia Martinez, Tania|||0000-0002-3428-3075 López Béjar, Manel|||0000-0001-9490-6126 Yeste Oliveras, Marc|||0000-0002-2209-340X Mercadé, Elena|||0000-0001-7828-2210 Mogas Amorós, Teresa|||0000-0002-6733-1328 |
| author |
Ordóñez-León, Erika Alina |
| author_facet |
Ordóñez-León, Erika Alina Martínez-Rodero, Iris|||0000-0001-7057-2045 Garcia Martinez, Tania|||0000-0002-3428-3075 López Béjar, Manel|||0000-0001-9490-6126 Yeste Oliveras, Marc|||0000-0002-2209-340X Mercadé, Elena|||0000-0001-7828-2210 Mogas Amorós, Teresa|||0000-0002-6733-1328 |
| author_role |
author |
| author2 |
Martínez-Rodero, Iris|||0000-0001-7057-2045 Garcia Martinez, Tania|||0000-0002-3428-3075 López Béjar, Manel|||0000-0001-9490-6126 Yeste Oliveras, Marc|||0000-0002-2209-340X Mercadé, Elena|||0000-0001-7828-2210 Mogas Amorós, Teresa|||0000-0002-6733-1328 |
| author2_role |
author author author author author author |
| dc.subject.none.fl_str_mv |
Cryopreservation Blastocyst Total cell number Inner cell mass TUNEL Embryo development Gene expression regulation |
| topic |
Cryopreservation Blastocyst Total cell number Inner cell mass TUNEL Embryo development Gene expression regulation |
| description |
This study aimed to assess the cryoprotectant role of exopolysaccharide (EPS) ID1, produced by Antarctic Pseudomonas sp., in the vitrification of in vitro-produced (IVP) bovine embryos. IVP day 7 (D7) and day 8 (D8) expanded blastocysts derived from cow or calf oocytes were vitrified without supplementation (EPS0) or supplemented with 10 µg/mL (EPS10) or 100 µg/mL (EPS100) EPS ID1. The effect of EPS ID1 was assessed in post-warming re-expansion and hatching rates, differential cell count, apoptosis rate, and gene expression. EPS100 re-expansion rates were significantly higher than those observed for the EPS0 and EPS10 treatments, regardless of culture length or oocyte source. EPS100 hatching rate was similar to the one of the fresh blastocysts except for those D7 blastocysts derived from calf oocytes. No differences were observed among EPS ID1 treatments when the inner cell mass, trophectoderm, and total cell number were assessed. Although apoptosis rates were higher (p ≤ 0.05) in vitrified groups compared to fresh embryos, EPS100 blastocysts had a lower number (p ≤ 0.05) of apoptotic nuclei than the EPS0 or EPS10 groups. No differences in the expression of BCL2, AQP3, CX43, and SOD1 genes between treatments were observed. Vitrification without EPS ID1 supplementation produced blastocysts with significantly higher BAX gene expression, whereas treatment with 100 µg/mL EPS ID1 returned BAX levels to those observed in non-vitrified blastocysts. Our results suggest that 100 µg/mL EPS ID1 added to the vitrification media is beneficial for embryo cryopreservation because it results in higher re-expansion and hatching ability and it positively modulates apoptosis. |
| publishDate |
2022 |
| dc.date.none.fl_str_mv |
2 2022-01-01 2022 2022-01-01 |
| dc.type.none.fl_str_mv |
Article http://purl.org/coar/resource_type/c_6501 VoR http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| dc.type.openaire.fl_str_mv |
info:eu-repo/semantics/article |
| format |
article |
| dc.identifier.none.fl_str_mv |
https://ddd.uab.cat/record/260299 https://dx.doi.org/urn:doi:10.3390/ijms23137069 |
| url |
https://ddd.uab.cat/record/260299 https://dx.doi.org/urn:doi:10.3390/ijms23137069 |
| dc.language.none.fl_str_mv |
Inglés eng |
| language_invalid_str_mv |
Inglés |
| language |
eng |
| dc.relation.none.fl_str_mv |
Agencia Estatal de Investigación https://doi.org/10.13039/501100011033 PID2020-116531RB-I00 Agencia Estatal de Investigación https://doi.org/10.13039/501100011033 BES-2017-081962 |
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open access http://purl.org/coar/access_right/c_abf2 https://creativecommons.org/licenses/by/4.0/ |
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info:eu-repo/semantics/openAccess |
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open access http://purl.org/coar/access_right/c_abf2 https://creativecommons.org/licenses/by/4.0/ |
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openAccess |
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