DOI QR코드

DOI QR Code

Detrimental Effect of Bovine Serum Albumin in a Maturation Medium on Embryonic Development after Somatic Cell Nuclear Transfer in Pigs

  • Lee, Hanna (Division of Applied Animal Science, College of Animal Life Science, Kangwon National University) ;
  • Lee, Yongjin (College of Veterinary Medicine, Kangwon National University) ;
  • Park, Bola (College of Veterinary Medicine, Kangwon National University) ;
  • Elahi, Fazle (College of Veterinary Medicine, Kangwon National University) ;
  • Lee, Joohyeong (College of Veterinary Medicine, Kangwon National University) ;
  • Choi, Jung Hoon (College of Veterinary Medicine, Kangwon National University) ;
  • Lee, Seung Tae (Division of Applied Animal Science, College of Animal Life Science, Kangwon National University) ;
  • Park, Choon-Keun (Division of Applied Animal Science, College of Animal Life Science, Kangwon National University) ;
  • Hyun, Sang-Hwan (Laboratory of Veterinary Embryology and Biotechnology, College of Veterinary Medicine, Chungbuk National University) ;
  • Lee, Eunsong (College of Veterinary Medicine, Kangwon National University)
  • Received : 2014.11.21
  • Accepted : 2014.12.16
  • Published : 2014.12.31

Abstract

This study was designed to evaluate the effect of bovine serum albumin (BSA) in a maturation medium on oocyte maturation and embryonic development in pigs. Immature pig oocytes were matured for 44 h in a medium supplemented with 0.4% (w/v) BSA, 0.1% (w/v) polyvinyl alcohol (PVA), or 10% (v/v) pig follicular fluid (PFF). After IVM, oocytes reached metaphase II stage were activated for parthenogenesis (PA) or used as cytoplasts for somatic cell nuclear transfer (SCNT). Nuclear maturation (89.5%, 90.7% and 91.3% for BSA, PVA and PFF, respectively) and intraoocyte glutathione contents (1.20, 1.16 and 1.00 pixels/oocyte for BSA, PVA and PFF, respectively) were not altered by the macromolecules added to maturation medium. IVM of oocytes in a medium containing BSA (21.4%) and PVA (20.7%) showed significantly lower blastocyst formation after PA than culture in medium with PFF (39.2%). After SCNT, oocytes matured in medium with BSA showed decreased embryonic development to the blastocyst stage (9.2%) compared to those matured in medium with PFF (28.9%), while 23.6% of SCNT oocytes matured in medium with PVA developed to the blastocyst stage. When the effect of BSA in a maturation medium during the first 22 h and the second 22 h of IVM in combination with PFF or PVA was examined, PVA-BSA showed a higher nuclear maturation (94.1%) than BSA-PFF (84.5%). However, there was no significant difference in the blastocyst formation among tested combinations (47.3, 52.2, 50.0, 44.4 and 49.0% for PFF-PFF, PFF-BSA, PVA-BSA, BSA-PVA and BSA-PFF, respectively). Our results demonstrate that BSA and PVA added to maturation medium can support oocyte maturation comparable to PFF-supplemented medium. However, maturation of oocytes in a BSA-containing medium decreases embryonic development after PA and SCNT when compared with the medium supplemented with PFF.

Keywords

References

  1. Abeydeera LR, Wang WH, Cantley TC, Rieke A, Murphy CN, Prather RS and Day BN. 2000. Development and viability of pig oocytes matured in a protein-free medium containing epidermal growth factor. Theriogenology 54:787-797. https://doi.org/10.1016/S0093-691X(00)00390-3
  2. Abeydeera LR, Wang WH, Prather RS and Day BN. 1998. Maturation in vitro of pig oocytes in protein-free culture media: fertilization and subsequent embryo development in vitro. Biol. Reprod. 58:1316-1320. https://doi.org/10.1095/biolreprod58.5.1316
  3. Camaioni A, Hascall VC, Yanagishita M and Salustri A. 1993. Effects of exogenous hyaluronic acid and serum on matrix organization and stability in the mouse cumulus cell-oocyte complex. J. Biol. Chem. 268:20473-20481.
  4. Chen L, Wert SE, Hendrix EM, Russell PT, Cannon M and Larsen WJ. 1990. Hyaluronic acid synthesis and gap junction endocytosis are necessary for normal expansion of the cumulus mass. Mol. Reprod. Dev. 26:236-247. https://doi.org/10.1002/mrd.1080260307
  5. De Matos DG and Furnus CC. 2000. The importance of having high glutathione (GSH) level after bovine in vitro maturation on embryo development: effect of ${\beta}$-mercaptoethanol, cysteine and cystine. Theriogenology 53:761-771. https://doi.org/10.1016/S0093-691X(99)00278-2
  6. Duque P, Hidalgo CO, Gomez E, Pintado B, Facal N and Diez C. 2003. Macromolecular source as dependent on osmotic pressure and water source: Effects on bovine in vitro embryo development and quality. Reprod. Nutr. Dev. 43:487-496. https://doi.org/10.1051/rnd:2004007
  7. Eckert J and Niemann H. 1995. In vitro maturation, fertilization and culture to blastocysts of bovine oocytes in proteinfree media. Theriogenology 43:1211-1225. https://doi.org/10.1016/0093-691X(95)00093-N
  8. Eppig JJ. 1982. The relationship between cumulus cell-oocyte coupling, oocyte meiotic maturation, and cumulus expansion. Dev. Biol. 89:268-272. https://doi.org/10.1016/0012-1606(82)90314-1
  9. Eppig JJ. 1991. Intercommunication between mammalian oocytes and companion somatic cells. Bioessays 13:569-574. https://doi.org/10.1002/bies.950131105
  10. George F, Daniaux C, Genicot G, Verhaeghe B, Lambert P and Donnay I. 2008. Set up of a serum-free culture system for bovine embryos: embryo development and quality before and after transient transfer. Theriogenology 69:612-623. https://doi.org/10.1016/j.theriogenology.2007.11.008
  11. Geshi M, Takenouchi N, Yamauchi N and Nagai T. 2000. Effects of sodium pyruvate in nonserum maturation medium on maturation, fertilization, and subsequent development of bovine oocytes with or without cumulus cells. Biol. Reprod. 63: 1730-1734. https://doi.org/10.1095/biolreprod63.6.1730
  12. Gray CW, Morgan PM and Kane MT. 1992. Purification of an embryotrophic factor from commercial bovine serum albumin and its identification as citrate. J. Reprod. Fertil. 94: 471-480. https://doi.org/10.1530/jrf.0.0940471
  13. Hong J and Lee E. 2007. Intrafollicular amino acid concentration and the effect of amino acids in a defined maturation medium on porcine oocyte maturation, fertilization, and preimplantation development. Theriogenology 68:728-735. https://doi.org/10.1016/j.theriogenology.2007.06.002
  14. Kane MT. 1985. A low molecular weight extract of bovine serum albumin stimulates rabbit blastocyst cell division and expansion in vitro. J. Reprod. Fertil. 73:147-150. https://doi.org/10.1530/jrf.0.0730147
  15. Kishida R, Lee ES and Fukui Y. 2004. In vitro maturation of porcine oocytes using a defined medium and developmental capacity after intracytoplasmic sperm injection. Theriogenology 62:1663-1676. https://doi.org/10.1016/j.theriogenology.2004.03.008
  16. Lee J, Lee Y, Park B, Elahi F, Jeon Y, Hyun S-H and Lee E. 2014. Developmental competence of IVM pig oocytes after SCNT in relation to the shrinkage pattern induced by hyperosmotic treatment. Theriogenology 81:974-981. https://doi.org/10.1016/j.theriogenology.2014.01.022
  17. Liu RH, Li YH, Jiao LH, Wang XN, Wang H and Wang WH. 2002. Extracellular and intracellular factors affecting nuclear and cytoplasmic maturation of porcine oocytes collected from different sizes of follicles. Zygote 10:253-260. https://doi.org/10.1017/S0967199402002332
  18. Marei WF, Ghafari F and Fouladi-Nashta AA. 2012. Role of hyaluronic acid in maturation and further early embryo development of bovine oocytes. Theriogenology 78:670-677. https://doi.org/10.1016/j.theriogenology.2012.03.013
  19. Mingoti GZ, Garcia JM and Rosa-e-Silva AA. 2002. Steroidogenesis in cumulus cells of bovine cumulus-oocyte-complexes matured in vitro with BSA and different concentrations of steroids. Anim. Reprod. Sci. 69:175-186. https://doi.org/10.1016/S0378-4320(01)00187-7
  20. Mizushima S and Fukui Y. 2001. Fertilizability and developmental capacity of bovine oocytes cultured individually in a chemically defined maturation medium. Theriogenology 55:1431-1445. https://doi.org/10.1016/S0093-691X(01)00492-7
  21. Sakatani M, Suda I, Oki T, Kobayashi S, Kobayashi S and Takahashi M. 2007. Effects of purple sweet potato anthocyanins on development and intracellular redox status of bovine preimplantation embryos exposed to heat shock. J. Reprod. Dev. 53:605-614. https://doi.org/10.1262/jrd.18124
  22. Seli E, Zeyneloglu HB, Senturk LM, Bahtiyar OM, Olive DL and Arici A. 1998. Basic fibroblast growth factor: peritoneal and follicular fluid levels and its effect on early embryonic development. Fertil. Steril. 69:1145-1148. https://doi.org/10.1016/S0015-0282(98)00074-0
  23. Song K, Hyun SH, Shin T and Lee E. 2009. Post-activation treatment with demecolcine improves development of somatic cell nuclear transfer embryos in pigs by modifying the remodeling of donor nuclei. Mol. Reprod. Dev. 76:611-619. https://doi.org/10.1002/mrd.20989
  24. Sung LY, Du F, Xu J, Chang W, Nedambale TL, Zhang J, Jiang S, Tian XC and Yang X. 2004. The differential requirement of albumin and sodium citrate on the development of in vitro produced bovine embryos. Reprod. Nutr. Dev. 44:551-564. https://doi.org/10.1051/rnd:2004061
  25. Sutton ML, Gilchrist RB and Thompson JG. 2003. Effects of in-vivo and in-vitro environments on the metabolism of the cumulus-oocyte complex and its influence on oocyte developmental capacity. Hum. Reprod. Update 9:35-48. https://doi.org/10.1093/humupd/dmg009
  26. Suzuki C and Yoshioka K. 2006. Effects of amino acid supplements and replacement of polyvinyl alcohol with bovine serum albumin in porcine zygote medium. Reprod. Fertil. Dev. 18:789-795. https://doi.org/10.1071/RD06032
  27. Wan PC, Hao ZD, Zhou P, Wu Y, Yang L, Cui MS, Liu SR and Zeng SM. 2009. Effects of SOF and CR1 media on developmental competence and cell apoptosis of ovine in vitro fertilization embryos. Anim. Reprod. Sci. 114:279-288. https://doi.org/10.1016/j.anireprosci.2008.09.020
  28. Wang WH and Day BN. 2002. Development of porcine embryos produced by IVM/IVF in a medium with or without protein supplementation: effects of extracellular glutathione. Zygote 10:109-115. https://doi.org/10.1017/S0967199402002150
  29. Wydooghe E, Heras S, Dewulf J, Piepers S, Van den Abbeel E, De Sutter P, Vandaele L and Van Soom A. 2014. Replacing serum in culture medium with albumin and insulin, transferrin and selenium is the key to successful bovine embryo development in individual culture. Reprod. Fertil. Dev. 26:717-724. https://doi.org/10.1071/RD13043
  30. Yamauchi N and Nagai T. 1999. Male pronuclear formation in denuded porcine oocytes after in vitro maturation in the presence of cysteamine. Biol. Reprod. 61:828-833. https://doi.org/10.1095/biolreprod61.3.828
  31. Yong HY and Lee E. 2007. Presence of intact cumulus cells during in vitro fertilization inhibits sperm penetration but improves blastocyst formation in vitro. J. Emb. Trans. 22: 1-7.
  32. You J, Kim J and Lee E. 2009. Effect of macromolecules in maturation medium on oocyte maturation and embryonic development after parthenogenesis and nuclear transfer in pigs. J. Emb. Trans. 24:97-104.
  33. You J, Kim J, Lim J and Lee E. 2010. Anthocyanin stimulates in vitro development of cloned pig embryos by increasing the intracellular glutathione level and inhibiting reactive oxygen species. Theriogenology 74:777-785. https://doi.org/10.1016/j.theriogenology.2010.04.002
  34. You J, Lee J, Hyun SH and Lee E. 2012. L-carnitine treatment during oocyte maturation improves in vitro development of cloned pig embryos by influencing intracellular glutathione synthesis and embryonic gene expression. Theriogenology 78:235-243. https://doi.org/10.1016/j.theriogenology.2012.02.027
  35. Zhang L, Jiang S, Wozniak PJ, Yang X and Godke RA. 1995. Cumulus cell function during bovine oocyte maturation, fertilization, and embryo development in vitro. Mol. Reprod. Dev. 40:338-344. https://doi.org/10.1002/mrd.1080400310