Czech J. Anim. Sci., 2010, 55(7):267-275 | DOI: 10.17221/298/2009-CJAS

Recombinant human activin A promotes development of bovine somatic cell nuclear transfer embryos matured in vitro

S. Hua, J. Lan, Y.G. Liu, Y.L. Song, J. Liu, Y.S. Wang, T. Zhang, Y. Zhang
College of Veterinary Medicine, Northwest A and F University, Yangling, Shaanxi Province, China

To improve the culture system of bovine somatic cell nuclear transfer (SCNT) embryos, we studied the effects of activin A on developmental competence of bovine SCNT embryos during the early development stage based on the traditional culture method, and analyzed the expression level of the genes related to blastocyst hatching (Na/K-ATPase, Glut-1) and related to activin A signalling pathway (ActRII and Smad2). We generated the bovine SCNT embryo using a Holstein cow oocyte as recipient cytoplasm and a foetal ear fibroblast (Holstein cow, 120 days) as donor cell. The embryos were cultured as follows: experiment 1, the addition of activin A at the concentrations of 0 (control), 20 (M1-20), 40 (M1-40) or 80 ng/ml (M1-80) to the media during the first three days and no addition during the subsequent 5 days; experiment 2, no addition of activin A to the media during the first 3 days and the addition of activin A at the concentrations of 0 (control), 20 (M2-20), 40 (M2-40) or 80 ng/ml (M2-80) during the subsequent 5 days. The results indicated that the blastocyst formation rate and hatching rate, and total blastomere numbers as well as ICM/TE obtained in experiment 1 were not significantly different from the control group (P > 0.05). In contrast, these values obtained in experiment 2 were significantly higher than in the control group (P < 0.05). In addition, the relative abundance (ratio to GAPDH mRNA) of each gene (Glut-1, ActR II and Smad2) was not significantly different among the treatments in the experiment. The expression levels of 4 genes (Na/K-ATPase, Glut-1, ActR II and Smad2) in blastocysts obtained in experiment 2 were higher than those obtained in experiment 1. In conclusion, the present study suggests that the addition of activin A to the culture media from day 4 to day 8 can enhance the developmental competence of bovine SCNT embryos.

Keywords: activin A; SCNT; embryo development; bovine

Published: July 31, 2010  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
Hua S, Lan J, Liu YG, Song YL, Liu J, Wang YS, et al.. Recombinant human activin A promotes development of bovine somatic cell nuclear transfer embryos matured in vitro. Czech J. Anim. Sci. 2010;55(7):267-275. doi: 10.17221/298/2009-CJAS.
Download citation

References

  1. Albano R.M., Groome N., Smith J.C. (1993): Activins are expressed in preimplantation mouse embryos and in ES and EC cells and are regulated on their differentiation. Development, 117, 711-723. Go to original source... Go to PubMed...
  2. Balasubramanian S., Son W.J., Kumar B.M., Ock S.A., Yoo J.G., Im G.S., Choe S.Y., Rho G.J. (2007): Expression pattern of oxygen and stress-responsive gene transcripts at various developmental stages of in vitro and in vivo preimplantation bovine embryos. Theriogenology, 68, 265-275. Go to original source... Go to PubMed...
  3. Barnes F.L., Eyestone W.H. (1990): Early cleavage and the maternal zygotic transition in bovine embryos. Theriogenology, 33, 141-152. Go to original source...
  4. Barnes F.L., First N.L. (1991): Embryonic transcription in in vitro cultured bovine embryos. Molecular Reproduction and Development, 29, 117-123. Go to original source... Go to PubMed...
  5. Camous S., Heyman Y., Meziou W., Ménézo Y. (1984): Cleavage beyond the block stage and survival after transfer of early bovine embryos cultured with trophoblastic vesicles. Journal of Reproduction and Fertility, 72, 479-485. Go to original source... Go to PubMed...
  6. Coss D., Thackray V.G., Deng C.X., Mellon. P.L. (2005): Activin regulates luteinizing hormone beta-subunit gene expression through Smad-binding and homeobox elements. Molecular Endocrinology, 19, 2610-2623. Go to original source... Go to PubMed...
  7. Enright B.P., Lonergan P., Dinnyes A., Fair T., Ward F.A., Yang X., Boland M.P. (2000): Culture of in vitro produced bovine zygotes in vitro vs in vivo: implications for early embryo development and quality. Theriogenology, 54, 659-673. Go to original source... Go to PubMed...
  8. Gandolfi F., Modina S., Brevini T.A., Passoni L., Artini P., Petraglia F., Lauria A. (1995): Activin beta A subunit is expressed in bovine oviduct. Molecular Reproduction and Development, 40, 286-291. Go to original source... Go to PubMed...
  9. Hirai S., Matsumoto H., Moriya N.H., Kawachi H., Yano H. (2007): Follistatin rescues the inhibitory effect of activin A on the differentiation of bovine preadipocyte. Domestic Animal Endocrinology, 33, 269-280. Go to original source... Go to PubMed...
  10. Hossein M.S., Jeong Y.W., Park S.W., Kim J.J., Lee E., Ko K.H., Kim H.S., Kim Y.W., Hyun S.H., Shin T., Hawthorne L., Hwang W.S. (2009): Obtaining multiple offspring of a specific canine genotype by somatic cell nuclear transfer. Cloning Stem Cells, 11, 123-130. Go to original source... Go to PubMed...
  11. Hua S., Zhang Y., Li X.C., Ma L.B., Cao J.W., Dai J.P., Li R. (2007): Effects of granulosa cell mitochondria transfer on the early development of bovine embryos in vitro. Cloning Stem Cells, 9, 237-246. Go to original source... Go to PubMed...
  12. Jones R.L., Kaitu'u-Lino T.J., Nie G., Sanchez-Partida L.G., Findlay J.K., Salamonsen L.A. (2006): Complex expression patterns support potential roles for maternally derived activins in the establishment of pregnancy in mouse. Reproduction, 132, 799-810. Go to original source... Go to PubMed...
  13. Khatir H., Anouassi A., Tibary A. (2007): Quality and developmental ability of dromedary (Camelus dromedarius) embryos obtained by IVM/IVF, in vivo matured/IVF or in vivo matured/fertilized oocytes. Reproduction in Domestic Animals, 42, 263-270. Go to original source... Go to PubMed...
  14. Koo D.B., Kang Y.K., Choi Y.H., Sun P.J., Ha-Na K., Bong O.K., Dong-Soo S., Humdai P., Kyung-Kwang L., YongMahn H. (2002): Aberrant allocations of inner cell mass and trophectoderm cells in bovine nuclear transfer blastocysts. Biology of Reproduction, 67, 487-492. Go to original source... Go to PubMed...
  15. Manova K., Paynton B.V., Bachvarova R.F. (1992): Expression of activins and TGF beta 1 and beta 2 RNAs in early postimplantation mouse embryos and uterine decidua. Mechanisms of Development, 36, 141-152. Go to original source... Go to PubMed...
  16. Mtango N.R., Varisanga M.D., Dong Y.J., Rajamahendran R., Suzuki T. (2003): Growth factors and growth hormone enhance in vitro embryo production and post-thaw survival of vitrified bovine blastocysts. Theriogenology, 59, 1393-1402. Go to original source... Go to PubMed...
  17. Orimo T., Taga M., Matsui H., Minaguchi H. (1996): The effect of activin-A on the development of mouse preimplantation embryos in vitro. Journal of Assisted Reproduction and Genetics, 13, 669-674. Go to original source... Go to PubMed...
  18. Park J.E., Oh H.J., Hong S.G., Jang G., Kim M.K., Lee B.C. (2008): Effects of activin A on the in vitro development and mRNA expression of bovine embryos cultured in chemically-defined two-step culture medium. Reproduction in Domestic Animals, Digital object identifier doi: 10.1111/j.1439-0531.2008.01306.x Go to original source... Go to PubMed...
  19. Rieger D., Loskutoff N.M., Betteridge K.J. (1992): Developmentally related changes in the uptake and metabolism of glucose, glutamine and pyruvate by cattle embryos produced in vitro. Reproduction, Fertility, and Development, 4, 547-557. Go to original source... Go to PubMed...
  20. Rizos D., Ward F., Duffy P., Boland M.P., Lonergan P. (2002): Consequences of bovine oocyte maturation, fertilization or early embryo development in vitro versus in vivo: implications for blastocyst yield and blastocyst quality. Molecular Reproduction and Development, 61, 234-248. Go to original source... Go to PubMed...
  21. Silva C.C., Knight P.C. (1998): Modulatory actions of activin A and follistatin on the developmental competence of in vitro-matured bovine oocytes. Biology of Reproduction, 58, 558-565. Go to original source... Go to PubMed...
  22. Stock A.E., Woodruff T.K., Smith L.C. (1997): Effects of inhibin A and activin A during in vitro maturation of bovine oocytes in hormone- and serum-free medium. Biology of Reproduction, 56, 1559-1564. Go to original source... Go to PubMed...
  23. Takahashi Y., First N.L. (1992): In vitro development of bovine one-cell embryos: Influence of glucose, lactate, pyruvate, amino acids and vitamins. Theriogenology, 37, 963-978. Go to original source... Go to PubMed...
  24. Vorbrodt A., Konwinski M., Solter D., Koprowski H. (1997): Ultrastructural cytochemistry of membranebound phosphatases in preimplantation mouse embryos. Developmental Biology, 55, 117-134. Go to original source... Go to PubMed...
  25. Watson A.J., Kidder G.M. (1988): Immunofluorescence assessment of the timing of appearance and cellular distribution of Na/K-ATPase during mouse embryogenesis. Developmental Biology, 126, 80-90. Go to original source... Go to PubMed...
  26. Wrenzycki C., Herrmann D., Niemann H. (2003): Timing of blastocyst expansion affects spatial messenger RNA expression patterns of genes in bovine blastocysts produced in vitro. Biology of Reproduction, 68, 2073-2080. Go to original source... Go to PubMed...
  27. Yoshioka K., Kamomae H. (1996): Recombinant human activin A stimulates development of bovine one-cell embryos matured and fertilized in vitro. Molecular Reproduction and Development, 45, 151-156. Go to original source...
  28. Yoshioka K., Suzuki C., Iwamura S. (1998): Activin A and follistatin regulate developmental competence of in vitro-produced bovine embryos. Biology of Reproduction, 59, 1017-1022. Go to original source... Go to PubMed...
  29. Yoshioka K., Suzuki C., Iwamura S. (2000): Effects of activin A and follistatin on developmental kinetics of bovine embryos: cinematographic analysis in a chemi-cally defined medium. Journal of Reproduction and Fertility, 118, 119-125. Go to original source...

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY NC 4.0), which permits non-comercial use, distribution, and reproduction in any medium, provided the original publication is properly cited. No use, distribution or reproduction is permitted which does not comply with these terms.