Journals / Turkish Journal of Veterinary and Animal Sciences / 2012 / Cilt: 36 - Sayı: 4

The effects of oviductal cell co-culture and different gas mixtures on the development of bovine embryos in vitro

Pages
362–366
Publication Date
2012-04-01
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In conclusion, the addition of co-culture to B2 (5% CO2 atmosphere) and SOF (5% CO2, 5% O2, and 90% N2 atmosphere) media increased the rate of transferable embryos.

📌 3 Key Takeaways

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Objective & Hypothesis:The objective of the current study was to investigate the effects of the addition of oviduct co-culture to synthetic oviduct fluid (SOF) and Ménézo B2 media used in an in vitro study of cows, and the effects of different gas atmospheres (5% CO2 or 5% CO2, 5% O2, and 90% N2) on in vitro cultures.
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Key Findings & Data:Oocytes obtained through aspiration from the ovaries of slaughtered Holstein cows were washed and cultured within a TCM-199 maturation medium at 38.8 °C for 23 h.
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Conclusion & Impact:In conclusion, the addition of co-culture to B2 (5% CO2 atmosphere) and SOF (5% CO2, 5% O2, and 90% N2 atmosphere) media increased the rate of transferable embryos.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Key words: Cattle · embryo · oviduct co-culture

Abstract

The objective of the current study was to investigate the effects of the addition of oviduct co-culture to synthetic oviduct fluid (SOF) and Ménézo B2 media used in an in vitro study of cows, and the effects of different gas atmospheres (5% CO2 or 5% CO2, 5% O2, and 90% N2) on in vitro cultures. Oocytes obtained through aspiration from the ovaries of slaughtered Holstein cows were washed and cultured within a TCM-199 maturation medium at 38.8 °C for 23 h. Then the matured oocytes and thawed semen, prepared in accordance with the swim-up method, were incubated for fertilization within in vitro fertilization (IVF)-Tyrode's albumin lactate pyruvate (TALP) medium with an atmosphere including the combination of 5% CO2, 5% O2, and 90% N2 gas, at 38.8 °C for 18-24 h. Fertilized oocytes were distributed into 3 main groups: Group I: B2 (5% CO2), Group II: B2 medium (5% CO2, 5% O2, and 90% N2), and Group III: SOF (5% CO2, 5% O2, and 90% N2), and each group was divided into 2 subgroups, with and without oviduct co-culture cells, and were cultured for 9 days. The percentage of embryos that reached the blastocyst stage was 34.0%, 20.0%, and 32.3% in the co-culture group and 26.7% and 23.3% in the without co-culture group, respectively. Group III showed the highest development of expanded blastocyst stage (P < 0.01). In conclusion, the addition of co-culture to B2 (5% CO2 atmosphere) and SOF (5% CO2, 5% O2, and 90% N2 atmosphere) media increased the rate of transferable embryos.

Özet

The objective of the current study was to investigate the effects of the addition of oviduct co-culture to synthetic oviduct fluid (SOF) and Ménézo B2 media used in an in vitro study of cows, and the effects of different gas atmospheres (5% CO2 or 5% CO2, 5% O2, and 90% N2) on in vitro cultures. Oocytes obtained through aspiration from the ovaries of slaughtered Holstein cows were washed and cultured within a TCM-199 maturation medium at 38.8 °C for 23 h. Then the matured oocytes and thawed semen, prepared in accordance with the swim-up method, were incubated for fertilization within in vitro fertilization (IVF)-Tyrode's albumin lactate pyruvate (TALP) medium with an atmosphere including the combination of 5% CO2, 5% O2, and 90% N2 gas, at 38.8 °C for 18-24 h. Fertilized oocytes were distributed into 3 main groups: Group I: B2 (5% CO2), Group II: B2 medium (5% CO2, 5% O2, and 90% N2), and Group III: SOF (5% CO2, 5% O2, and 90% N2), and each group was divided into 2 subgroups, with and without oviduct co-culture cells, and were cultured for 9 days. The percentage of embryos that reached the blastocyst stage was 34.0%, 20.0%, and 32.3% in the co-culture group and 26.7% and 23.3% in the without co-culture group, respectively. Group III showed the highest development of expanded blastocyst stage (P < 0.01). In conclusion, the addition of co-culture to B2 (5% CO2 atmosphere) and SOF (5% CO2, 5% O2, and 90% N2 atmosphere) media increased the rate of transferable embryos.

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Cite This Article

ÖZDAŞ, Ö. B., CİRİT, Ü., BARAN, A., KAŞIKÇI, G. (2012). The effects of oviductal cell co-culture and different gas mixtures on the development of bovine embryos in vitro. Turkish Journal of Veterinary and Animal Sciences, Cilt: 36 - Sayı: 4, 362–366. https://ajindex.com/articles/122031

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References (11)

  1. Avery, B., Brandenhoff, H.R., Greve, T.: Development of in vitro matured and fertilized bovine embryos, cultured from days 1-5 post insemination in either Ménézo B2 medium or in HECM-6 medium. Th eriogenology, 1995; 44: 935-945.
  2. Özdaş, Ö.B., Pabuccuoğlu, S., İleri, İ.K.: Eff ects of monopotasium phosphate and oviduct cells on the in vitro fertilized mice embryos development. Medycyna Wet., 2006; 62: 281-284.
  3. Walker, S.K., Wade, M.G., Nancarrow, C.D., Kelleher, D.L, Boland, M.P.: Development of ovine embryos in synthetic oviductal fl uid containing amino acids at oviductal fl uid concentrations. Biol. Reprod. 1996; 55: 703-708.
  4. Rizos, D., Ramirez, M.A., Pintado, B., Lonergan, P., Gutierrez- Adan, A.: Culture of bovine embryos in intermediate host oviducts with emphasis on the isolated mouse oviduct. Th eriogenology, 2010; 73: 775-785.
  5. Fischer, B., Bavister, B.D.: Oxygen tension in the oviduct and uterus of rhesus monkeys, hamster and rabbits. J. Reprod. Fertil., 1993; 99: 673-679.
  6. Tervit, H.R., Whittingham, D.G., Rowson, L.E.: Successful culture in vitro of sheep and cattle ova. J. Reprod. Fertil., 1972; 30: 493-497.
  7. Rief, S., Sinowatz, F., Stojkovic, M., Einspanier, R., Wolf, E., Prelle, K.: Eff ects of novel co-culture system on development, metabolism and gene expression of bovine embryos produced in vitro. Reproduction, 2002; 124: 543-556.
  8. Goovaerts, I.G.F., Leroy, J.L.M.R., Soom, A. Van., Clercq, J.B.P. de, Andries S., Bols, P.E.J.: Eff ect of cumulus cell co-culture and oxygen tension in the in vitro developmental competence of bovine zygotes cultured singly. Th eriogenology, 2009; 71: 729- 738. Barnett, D.K, Bavister, B.D.: What is the relationship between the metabolism of preimplantation embryos and their developmental competence. Mol. Reprod. Dev., 1996; 43: 105- 133. 18 Moore, K., Bondioli, K.R.: Glycine and alanine supplementation of culture medium enhances development of in vitro matured and fertilized cattle embryos. Biol. Reprod., 1993; 48: 833-840.
  9. Vanroose, G., Van Soom, A., Kruif, A.: From co-culture to defi ned medium: state of the art and practical considerations. Reprod. Dom. Anim., 2001; 36: 25-28.
  10. Yuan, Y.Q., Van Soom, A., Coopman, F.O.J., Mintiens, K., Boerjan, M.L., Van Zeveren, A., Kruif, A., Peelman, L.J.: Infl uence of oxygen tension on apoptosis and hatching in bovine embryos cultured in vitro. Th eriogenology, 2003; 59, 1585-1596.
  11. Pinyopummintr, T., Bavister, B.D.: Energy substrate requirements for in vitro development of earl