Abstract

BackgroundThe in vitro culture of presumed zygotes derived from single cow ovum pick-up (OPU) is important for the production of quality blastocysts maintaining pedigree. The aim of the present study was to evaluate the agar chip-embedded helper embryo coculture system for single cow OPU-derived zygotes by assessing embryo quality.MethodsCumulus oocyte complexes (COCs) were collected from Hanwoo cows with high genetic merit twice a week using the ultra-sound guided OPU technique and from slaughterhouse ovaries. The Hanwoo cow COCs and slaughterhouse ovaries were matured in vitro, fertilized in vitro with thawed Hanwoo sperm and cultured for 24 h. The presumed zygotes were subsequently placed in three different culture systems: (1) control OPU (controlOPU) with single cow OPU-derived presumed zygotes (2~8); (2) agar chip-embedded slaughterhouse helper embryo coculture (agarOPU) with ten presumed zygotes including all presumed zygotes from a cow (2~8) and the rest from agar chip-embedded slaughterhouse presumed zygotes (8~2); and (3) slaughterhouse in vitro embryo production (sIVP) with ten slaughterhouse ovary-derived presumed zygotes, each in 50 μL droplets. Day 8 blastocysts were assayed for apoptosis and gene expression using real time PCR.ResultsThe coculture system promoted higher blastocyst development in OPU zygotes compared to control OPU zygotes cultured alone (35.2 vs. 13.9%; P < 0.01). Genes predicted to be involved in implantation failure and/or embryo resorption were down-regulated (P < 0.05) in control OPU zygotes (CD9, 0.4-fold; AKRAB1, 0.3-fold) and in cocultured zygotes (CD9, 0.3-fold; AKRAB1, 0.3-fold) compared to sIVP blastocysts (1.0-fold). Moreover, genes involved in implantation and/or normal calf delivery were up-regulated (P < 0.05 to P < 0.01) in control OPU zygotes (PGSH2, 5.0-fold; TXN, 4.3-fold; PLAU, 1.7-fold) and cocultured zygotes (PGSH2, 14.5-fold; TXN, 3.2-fold; PLAU, 6.8-fold) compared to sIVP (1.0-fold) blastocysts. However, the expression of PLAC8, TGF-β1, ODC1, ATP5A1 and CASP3 did not differ between the three culture groups.ConclusionsResults show that the agar chip-embedded helper embryo coculture system enhances developmental competence and embryo quality in cultures of limited numbers of high pedigree single cow OPU presumed zygotes.

Highlights

  • The in vitro culture of presumed zygotes derived from single cow ovum pick-up (OPU) is important for the production of quality blastocysts maintaining pedigree

  • Experimental design Three different culture systems were tested to evaluate embryo development in OPU and slaughterhouse presumed zygotes including: (1) “control OPU” with single cow OPU derived presumed zygotes (2~8 depending on availability), (2) “agar chip embedded slaughterhouse helper embryo coculture” with a threshold of total ten presumed zygotes including all presumed zygotes from a donor cow (2~8 depending on availability) and the rest from agar chip embedded slaughterhouse presumed zygotes (8~2 depending on OPU presumed zygotes) and (3) “slaughterhouse in vitro embryo production (IVP) control” with ten presumed slaughterhouse derived zygotes each in 50 μL droplets of In vitro culture (IVC) medium

  • In vitro embryo development efficiency Development rates up to the cleavage stage did not differ between the controlOPU group and the agar chip-embedded slaughterhouse helper embryo coculture (agarOPU) group; blastocyst development rates were

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Summary

Introduction

The in vitro culture of presumed zygotes derived from single cow ovum pick-up (OPU) is important for the production of quality blastocysts maintaining pedigree. Ultrasound-guided transvaginal ovum pick-up (OPU) in combination with conventional in vitro fertilization (IVF) has enabled the production of large numbers of embryos from high genetic merit donors of different ages and physiological conditions [1,2,3]. The efficiency of OPU-based in vitro embryo production (IVP) ranges between 11% in untreated cows to 30% in hormone-treated cows [2,5,6,7,8]. The number of COCs collected from a single cow during an OPU session varies from < 3 in non-stimulated cows [5] to > 9 in hormone-stimulated cows [8]. A culture system promoting consistent high blastocyst development and maintaining pedigree would be crucial to cattle breeding programs

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