dc.creatorMaruri, Alejandro
dc.creatorCruzans, Paula Romina
dc.creatorLorenzo, María Soledad
dc.creatorTello, Maria Fernanda
dc.creatorTeplitz, Gabriela Maia
dc.creatorCarou, María Clara
dc.creatorLombardo, Daniel Marcelo
dc.date.accessioned2020-01-29T20:40:44Z
dc.date.accessioned2022-10-14T22:05:05Z
dc.date.available2020-01-29T20:40:44Z
dc.date.available2022-10-14T22:05:05Z
dc.date.created2020-01-29T20:40:44Z
dc.date.issued2018-10
dc.identifierMaruri, Alejandro; Cruzans, Paula Romina; Lorenzo, María Soledad; Tello, Maria Fernanda; Teplitz, Gabriela Maia; et al.; Embryotrophic effect of a short-term embryo coculture with bovine luteal cells; Elsevier Science Inc; Theriogenology; 119; 10-2018; 143-149
dc.identifier0093-691X
dc.identifierhttp://hdl.handle.net/11336/96167
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4311900
dc.description.abstractThe coculture with somatic cells is an alternative to improve suboptimal in vitro culture (IVC) conditions and promote embryo development. Several cell types have been used for this purpose, but there is no information about using luteal cells in short-term coculture with embryos. Consequently, this study aimed to assess the effect of a short-term coculture of early bovine embryos-luteal cells on the in vitro development and embryo quality. Presumptive embryos were cultured from day 0 to day 2 in medium alone (control) or cocultured with bovine luteal cells (BLC-1). Then, embryos from both groups were cultured in medium alone from day 2 to day 8. The development rates on day 8 were compared between groups. The level of reactive oxygen species (ROS) and proliferation rates were evaluated in day 2 embryos and late apoptosis and proliferation rates were determined in day 7 blastocysts. Our results showed that the coculture with bovine luteal cells increased the blastocyst rate compared to the control (50.4% vs. 29.8%; P < 0.01), but there were no differences in the cleavage rates on day 2. The rate of stage 6 blastocysts was higher in the coculture (37.3% vs. 23.8% control; P < 0.01), without differences in the expansion and hatching rates compared to the control. The ROS level in day 2 embryos was higher in the coculture than the control (82 vs. 57.1; P < 0.05), and the cell proliferation rate was higher in the coculture (48% vs. 13% control; P < 0.01), without differences in the mean number of cells between groups. In day 7 blastocysts, the apoptosis rate decreased in the coculture with bovine luteal cells from day 0 to day 2 (4.1% vs. 10.9% control; P < 0.01), whereas the cell proliferation rate and the mean number of cells did not differ between groups. This is the first report of a short-term coculture of in vitro produced embryos and bovine luteal cells. Our model could be an alternative to increase the efficiency of the in vitro production of embryos in cattle.
dc.languageeng
dc.publisherElsevier Science Inc
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.theriogenology.2018.06.032
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0093691X18304291
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectBOVINE EMBRYO QUALITY
dc.subjectBOVINE LUTEAL CELLS
dc.subjectCOCULTURE
dc.subjectEMBRYOTROPHIC EFFECT
dc.titleEmbryotrophic effect of a short-term embryo coculture with bovine luteal cells
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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