Bovine oviductal and uterine fluid support in vitro embryo development

In order to mimic the maternal oviductal environment, we evaluated the effect of oviductal fluid (OF) and/or uterine fluid (UF) supplementation on in vitro embryo development and quality. In vitro-produced zygotes were cultured with 1.25% OF from Day 1 to Day 4 after insemination (OF group), 1.25% OF from Day 1 to Day 4 followed by 1.25% UF from Day 4 to Day 9 (OF+UF group) or 1.25% UF only from Day 4 to Day 9 (UF group). Control groups were cultured in the presence of synthetic oviduct fluid (SOF) supplemented with 3mgmL-1 bovine serum albumin (BSA) or 5% fetal calf serum (FCS). Supplementation of the culture medium with OF and/or UF (both at 1.25%) supported embryo development (Day 9 blastocyst rate 28.2-30.6%). At 72h after vitrification-warming, the survival of blastocysts from the OF and OF+UF groups was similar to that of blastocysts in the SOF+BSA group (61.0±5.7% and 62.8±6.4% vs 64.8±6.4% respectively), but significantly higher than that of blastocysts from the SOF+FCS group (31.6±4.9%; P<0.001). Blastocysts from the OF group exhibited upregulation of epigenetic genes (i.e. DNA methyltransferase 3α (DNMT3A) and insulin-like growth factor 2 receptor (IGF2R)), compared with expression in the SOF+FCS group (P<0.05). Whereas those from OF+UF and UF groups exhibited downregulation of oxidative stress genes compared to SOF+BSA and OF groups for glutathione peroxidase (GPX1) and to SOF+FCS, SOF+BSA and OF groups for chloride intracellular channel 1 (CLIC1) (P<0.05). In addition, accumulation of reactive oxygen species was lower in blastocysts from the OF, OF+UF and UF groups. In conclusion, the use of low concentrations of OF and UF in in vitro serum-free culture supports embryo development, with OF providing a better control of embryo methylation, whereas UF may have antioxidant activity.

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Main Authors: Hamdi, M., Lopera-Vasquez, R., Maillo, V., Sanchez-Calabuig, M. J., Núnez, C., Gutiérrez Adán, Alfonso, Rizos Dimitrios, Dimitrios
Format: journal article biblioteca
Language:English
Published: CSIRO Publishing 2018
Subjects:Culture medium, Gene expression, in vitro, Fertilisation,
Online Access:http://hdl.handle.net/20.500.12792/565
http://hdl.handle.net/10261/293626
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spelling dig-inia-es-10261-2936262023-02-20T10:30:22Z Bovine oviductal and uterine fluid support in vitro embryo development Hamdi, M. Lopera-Vasquez, R. Maillo, V. Sanchez-Calabuig, M. J. Núnez, C. Gutiérrez Adán, Alfonso Rizos Dimitrios, Dimitrios Culture medium Gene expression in vitro Fertilisation In order to mimic the maternal oviductal environment, we evaluated the effect of oviductal fluid (OF) and/or uterine fluid (UF) supplementation on in vitro embryo development and quality. In vitro-produced zygotes were cultured with 1.25% OF from Day 1 to Day 4 after insemination (OF group), 1.25% OF from Day 1 to Day 4 followed by 1.25% UF from Day 4 to Day 9 (OF+UF group) or 1.25% UF only from Day 4 to Day 9 (UF group). Control groups were cultured in the presence of synthetic oviduct fluid (SOF) supplemented with 3mgmL-1 bovine serum albumin (BSA) or 5% fetal calf serum (FCS). Supplementation of the culture medium with OF and/or UF (both at 1.25%) supported embryo development (Day 9 blastocyst rate 28.2-30.6%). At 72h after vitrification-warming, the survival of blastocysts from the OF and OF+UF groups was similar to that of blastocysts in the SOF+BSA group (61.0±5.7% and 62.8±6.4% vs 64.8±6.4% respectively), but significantly higher than that of blastocysts from the SOF+FCS group (31.6±4.9%; P<0.001). Blastocysts from the OF group exhibited upregulation of epigenetic genes (i.e. DNA methyltransferase 3α (DNMT3A) and insulin-like growth factor 2 receptor (IGF2R)), compared with expression in the SOF+FCS group (P<0.05). Whereas those from OF+UF and UF groups exhibited downregulation of oxidative stress genes compared to SOF+BSA and OF groups for glutathione peroxidase (GPX1) and to SOF+FCS, SOF+BSA and OF groups for chloride intracellular channel 1 (CLIC1) (P<0.05). In addition, accumulation of reactive oxygen species was lower in blastocysts from the OF, OF+UF and UF groups. In conclusion, the use of low concentrations of OF and UF in in vitro serum-free culture supports embryo development, with OF providing a better control of embryo methylation, whereas UF may have antioxidant activity. 2023-02-20T10:30:22Z 2023-02-20T10:30:22Z 2018 journal article Reproduction , Fertility and Development 30(7): 935-945 (2017) 1031-3613 http://hdl.handle.net/20.500.12792/565 http://hdl.handle.net/10261/293626 10.1071/RD17286 1448-5990 en none CSIRO Publishing
institution INIA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-inia-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del INIA España
language English
topic Culture medium
Gene expression
in vitro
Fertilisation
Culture medium
Gene expression
in vitro
Fertilisation
spellingShingle Culture medium
Gene expression
in vitro
Fertilisation
Culture medium
Gene expression
in vitro
Fertilisation
Hamdi, M.
Lopera-Vasquez, R.
Maillo, V.
Sanchez-Calabuig, M. J.
Núnez, C.
Gutiérrez Adán, Alfonso
Rizos Dimitrios, Dimitrios
Bovine oviductal and uterine fluid support in vitro embryo development
description In order to mimic the maternal oviductal environment, we evaluated the effect of oviductal fluid (OF) and/or uterine fluid (UF) supplementation on in vitro embryo development and quality. In vitro-produced zygotes were cultured with 1.25% OF from Day 1 to Day 4 after insemination (OF group), 1.25% OF from Day 1 to Day 4 followed by 1.25% UF from Day 4 to Day 9 (OF+UF group) or 1.25% UF only from Day 4 to Day 9 (UF group). Control groups were cultured in the presence of synthetic oviduct fluid (SOF) supplemented with 3mgmL-1 bovine serum albumin (BSA) or 5% fetal calf serum (FCS). Supplementation of the culture medium with OF and/or UF (both at 1.25%) supported embryo development (Day 9 blastocyst rate 28.2-30.6%). At 72h after vitrification-warming, the survival of blastocysts from the OF and OF+UF groups was similar to that of blastocysts in the SOF+BSA group (61.0±5.7% and 62.8±6.4% vs 64.8±6.4% respectively), but significantly higher than that of blastocysts from the SOF+FCS group (31.6±4.9%; P<0.001). Blastocysts from the OF group exhibited upregulation of epigenetic genes (i.e. DNA methyltransferase 3α (DNMT3A) and insulin-like growth factor 2 receptor (IGF2R)), compared with expression in the SOF+FCS group (P<0.05). Whereas those from OF+UF and UF groups exhibited downregulation of oxidative stress genes compared to SOF+BSA and OF groups for glutathione peroxidase (GPX1) and to SOF+FCS, SOF+BSA and OF groups for chloride intracellular channel 1 (CLIC1) (P<0.05). In addition, accumulation of reactive oxygen species was lower in blastocysts from the OF, OF+UF and UF groups. In conclusion, the use of low concentrations of OF and UF in in vitro serum-free culture supports embryo development, with OF providing a better control of embryo methylation, whereas UF may have antioxidant activity.
format journal article
topic_facet Culture medium
Gene expression
in vitro
Fertilisation
author Hamdi, M.
Lopera-Vasquez, R.
Maillo, V.
Sanchez-Calabuig, M. J.
Núnez, C.
Gutiérrez Adán, Alfonso
Rizos Dimitrios, Dimitrios
author_facet Hamdi, M.
Lopera-Vasquez, R.
Maillo, V.
Sanchez-Calabuig, M. J.
Núnez, C.
Gutiérrez Adán, Alfonso
Rizos Dimitrios, Dimitrios
author_sort Hamdi, M.
title Bovine oviductal and uterine fluid support in vitro embryo development
title_short Bovine oviductal and uterine fluid support in vitro embryo development
title_full Bovine oviductal and uterine fluid support in vitro embryo development
title_fullStr Bovine oviductal and uterine fluid support in vitro embryo development
title_full_unstemmed Bovine oviductal and uterine fluid support in vitro embryo development
title_sort bovine oviductal and uterine fluid support in vitro embryo development
publisher CSIRO Publishing
publishDate 2018
url http://hdl.handle.net/20.500.12792/565
http://hdl.handle.net/10261/293626
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AT sanchezcalabuigmj bovineoviductalanduterinefluidsupportinvitroembryodevelopment
AT nunezc bovineoviductalanduterinefluidsupportinvitroembryodevelopment
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