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Fertilization and early embryology: Established cell lines and their conditioned media support bovine embryo development during in-vitro culture
Authors:Myers, M.W.   Broussard, J.R.   Menezo, Y.   Prough, S.G.   Blackwell, J.   Blackwell, J.   Godke, R.A.   Thibodeaux, J.K.
Affiliation:In Vitro Fertilization Laboratory, Tulsa Center for Fertility and Women's Health 1145 South Utica, Suite 1209, Tulsa, OK 74104 1Departments of Dairy Louisiana State University Baton Rouge, LA 70803, USA 2Departments of INSA, Laboratorie de Biologie Villeurbanne 69621, France 3Departments of Animal Science, Louisiana State University Baton Rouge, LA 70803, USA
Abstract:These experiments were conducted to evaluate the ability ofdifferent somatic–cell monolayers or conditioned mediumfrom somatic cells for supporting bovine embryo developmentin vitro. In the first experiment, bovine embryos (2- to 4-cells)were allocated randomly to a control (medium 199 with 10% fetalbovine serum and antibiotics) group or co-cultured with bovineoviduct epithelial (BOEC), buffalo rat liver (BRL), Madin Darbybovine kidney (MDBK) or African green monkey kidney (Vero) cells.In the second experiment, bovine embryos (1-cell) were allocatedrandomly to the following groups: control medium or conditionedmedium from BOEC, BRL, MDBK and Vero monolayers. In both experiments,development to the blastocyst stage was assessed after 8 daysof incubation at 39°C and 5% CO2 In Experiment 1, co-cultureimproved development to the blastocyst stage compared with controlmedium alone, and the highest development was observed afterco–culture with BOEC. In Experiment 2, conditioned mediumenhanced development to morulae and blastocysts compared withthe control medium; however, no differences were detected amongdifferent cell supports. These results indicate that both co-cultureand conditioned medium from different cell monolayers supporteddevelopment to the blastocyst stage at a higher efficiency thancontrol medium alone.
Keywords:bovine embryos/co-culture/in-vitro fertilization
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