dc.creatorPeralta Troncoso, Óscar
dc.creatorBucher, Danai
dc.creatorFernández, Ana
dc.creatorBerland, Marco
dc.creatorStrobel, Pablo
dc.creatorRamírez, Alfredo
dc.creatorConcha, Ilona I.
dc.creatorRatto, Marcelo H.
dc.date.accessioned2014-01-29T15:38:02Z
dc.date.accessioned2019-04-25T23:36:29Z
dc.date.available2014-01-29T15:38:02Z
dc.date.available2019-04-25T23:36:29Z
dc.date.created2014-01-29T15:38:02Z
dc.date.issued2013-06-24
dc.identifierREPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY Volume: 11
dc.identifierDOI: 10.1186/1477-7827-11-55
dc.identifierhttp://repositorio.uchile.cl/handle/2250/122514
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/2426867
dc.description.abstractBackground: The objectives of the study were to characterize the expression of the α- and β-subunits of granulocyte-macrophage colony stimulating factor (GM-CSF) receptor in bovine cumulus cells and oocytes and to determine the effect of exogenous GM-CSF on cumulus cells expansion, oocyte maturation, IGF-2 transcript expression and subsequent competence for embryonic development. Methods: Cumulus-oocyte complexes (COC) were obtained by aspirating follicles 3- to 8-mm in diameter with an 18 G needle connected to a vacuum pump at −50 mmHg. Samples of cumulus cells and oocytes were used to detect GM- CSF receptor by immunofluorescence. A dose–response experiment was performed to estimate the effect of GM-CSF on cumulus cell expansion and nuclear/cytoplasmic maturation. Also, the effect of GM-CSF on IGF-2 expression was evaluated in oocytes and cumulus cells after in vitro maturation by Q-PCR. Finally, a batch of COC was randomly assigned to in vitro maturation media consisting of: 1) synthetic oviductal fluid (SOF, n = 212); 2) synthetic oviductal fluid supplemented with 100 ng/ml of GM-CSF (SOF + GM-CSF, n = 224) or 3) tissue culture medium (TCM 199, n = 216) and then subsequently in vitro fertilized and cultured for 9 days. Results: Immunoreactivity for both α and β GM-CSF receptors was localized in the cytoplasm of both cumulus cells and oocytes. Oocytes in vitro matured either with 10 or 100 ng/ml of GM-CSF presented a higher (P < 0.05) cumulus cells expansion than that of the control group (0 ng/ml of GM-CSF). GM-CSF did not affect the proportion of oocytes in metaphase II, cortical granules dispersion and IGF-2 expression. COC exposed to 100 ng/ml of GM-CSF during maturation did not display significant differences in terms of embryo cleavage rate (50.4% vs. 57.5%), blastocyst development at day 7 (31.9% vs. 28.7%) and at day 9 (17.4% vs. 17.9%) compared to untreated control (SOF alone, P = 0.2). Conclusions: GM-CSF enhanced cumulus cell expansion of in vitro matured bovine COC. However, GM-CSF did not increase oocyte nuclear or cytoplasmic maturation rates, IGF-2 expression or subsequent embryonic development.
dc.languageen
dc.publisherBIOMED CENTRAL LTD
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.subjectGM-CSF
dc.titleGranulocyte-macrophage colony stimulating factor (GM-CSF) enhances cumulus cell expansion in bovine oocytes
dc.typeArtículos de revistas


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