The Impact of Two Embryo Culture Media, Synthetic Oviduct Fluid and Commercial BO, on pre-and post-Implantation Development of Cloned SAANEN Goat Embryos

Document Type : Original Article

Authors

1 Department of Animal Biotechnology, Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran

2 Department of Clinical Studies, School of Veterinary Medicine, Shahid Bahonar University of Kerman, Kerman, Iran

Abstract

Background: Somatic cell nuclear transfer (SCNT) is an approach for the propagation of elite animals. In vitro condition, especially the composition of culture media has a profound effect on the developmental competency of in vitro derived e mbryos. There are limited studies evaluating the effect of culture media on SCNT outcomes. To address this gap, we compare the effect of two culture media synthetic oviduct fluid (SOF) vs. commercial bracket-oliphant (BO) on developmental comptenecy.
Materials and Methods: In this experimental study, embryos derived from in vitro fertilized (IVF) and SCNT were cultured in both BO and SOF media for 7 days. In addition to the assessment of cleavage and blastocyst on day 3, and 7, the quantitative expression of 16 genes in theresultant blastocysts were assessed. The resultant SCNT blastocysts from SOF and BO groups were also transferred to the synchronized recipient for developmental competency to term.
Results: The blastocyst rate in the BO medium was significantly higher than that of the SOF medium in the SCNT group (P<0.05). All of the examined genes showed increased expression levels in SCNT blastocyst in both media compared to IVF Blastocyst. In the IVF group, Oct4, Bmpr1, and Gcn5 showed significantly higher expression in the SOF medium compared to the BO medium while Akt, Fgfr4, Sox2 showed significantly lower expression in the SOF medium compared to the BO medium. In the SCNT group, Fgfr4, Gcn5, Fzd, Ctnnb, Bmpr1, and Fgfr4 showed significantly higher expression in SOF compared to BO derived blastocyst.
Conclusion: It appears that in SCNT blastocysts, gene regulation is less controlled compared to IVF ones, irrespective of the type of medium. In addition, there are differences regarding certain genes expressions between IVF and SCNT derived blastocysts between SOF and BO, reiterating that culture composition affects developmental competency and gene expression.

Keywords


  1. Tríbulo P, Rivera RM, Obando MSO, Jannaman EA, Hansen PJ. Production and culture of the bovine embryo. Methods Mol Biol. 2019; 2006: 115-129.
  2. Petersen CG, Mauri AL, Vagnini LD, Renzi A, Petersen B, Matilla MC, et al. Randomized comparison of two commercial culture me­dia (Cook and Vitrolife) for embryo culture after IMSI. JBRA Assist Reprod. 2019; 23(1): 33-36.
  3. Takahashi Y, First NL. In vitro development of bovine one-cell em­bryos: influence of glucose, lactate, pyruvate, amino acids and vi­tamins. Theriogenology. 1992; 37(5): 963-978.
  4. Ménézo Y, Lichtblau I, Elder K. New insights into human pre-im­plantation metabolism in vivo and in vitro. J Assist Reprod Genet. 2013; 30(3): 293-303.
  5. Kleijkers SHM, van Montfoort APA, Bekers O, Coonen E, Derhaag JG, Evers JLH, et al. Ammonium accumulation in commercially available embryo culture media and protein supplements during storage at 2–8°C and during incubation at 37°C. Hum Reprod. 2016; 31(6): 1192-1199.
  6. Simopoulou M, Sfakianoudis K, Rapani A, Giannelou P, Anifandis G, Bolaris S, et al. Considerations regarding embryo culture condi­tions: from media to epigenetics. In Vivo. 2018; 32(3): 451-460.
  7. Mohd-Fazirul M, Nor-Ashikin MNK, Kamsani YS, Sharaniza Ab-Rahim, Norhazlin JMY, Wan-Hafizah WJ, et al. Comparison of the effects of three commercial media on preimplantation mouse em­bryo development and morphological grading. Biomed Res. 2015; 26(3): 477-484. 
  8. Morbeck DE, Baumann NA, Oglesbee D. Composition of single-step media used for human embryo culture. Fertil Steril. 2017; 107(4): 1055-1060. e1. 
  9. López-Pelayo I, Gutiérrez-Romero JM, Armada AIM, Calero-Ruiz MM, Acevedo-Yagüe PJM. Comparison of two commercial em­bryo culture media (SAGE-1 step single medium vs. G1-PLUS™/G2-PLUS™ sequential media): influence on in vitro fertilization outcomes and human embryo quality. JBRA Assist Reprod. 2018; 22(2): 128-133. 
  1. Hemkemeyer SA, Schwarzer C, Boiani M, Ehmcke J, Le Gac S, Schlatt S, et al. Effects of embryo culture media do not persist af­ter implantation: a histological study in mice. Hum Reprod. 2014; 29(2): 220-233.
  2. Soto-Heras S, Menéndez-Blanco I, Catalá MG, Izquierdo D, Thompson JG, Paramio MT. Biphasic in vitro maturation with C-type natriuretic peptide enhances the developmental competence of juvenile-goat oocytes. PLoS One. 2019; 14(8): e0221663.
  3. Deng M, Liu Z, Chen B, Wan Y, Yang H, Zhang Y, et al. Aberrant DNA and histone methylation during zygotic genome activation in goat cloned embryos. Theriogenology. 2020; 148: 27-36.
  4. Menéndez-Blanco I, Soto-Heras S, Catalá MG, Piras AR, Izquierdo D, Paramio MT. Effect of vitrification of in vitro matured prepubertal goat oocytes on embryo development after parthenogenic activa­tion and intracytoplasmic sperm injection. Cryobiology. 2020; 93: 56-61.
  5. Yao T, Asayama Y. Human preimplantation embryo culture media: past, present, and future. J Mamm Ova Res. 2016; 33(1): 17-34.
  6. Sfontouris IA, Kolibianakis EM, Lainas GT, Petsas GK, Tarlatzis BC, Lainas TG. Blastocyst development in a single medium com­pared to sequential media: a prospective study with sibling oo­cytes. Reprod Sci. 2017; 24(9): 1312-1318.
  7. Kij B, Kochan J, Nowak A, Niżański W, Prochowska S, Fryc K, et al. Using time lapse monitoring for determination of morphological defect frequency in feline embryos after in vitro fertilization (IVF). Animals (Basel). 2020; 10(1): 3.
  8. Salilew-Wondim D, Tesfaye D, Hoelker M, Schellander K. Embryo transcriptome response to environmental factors: implication for its survival under suboptimal conditions. Animal Reprod Sci. 2014; 149(1-2): 30-38.
  9. Song H, Li H, Huang M, Xu D, wang Z, Wang F. Big animal cloning using transgenic induced pluripotent stem cells: a case study of goat transgenic induced pluripotent stem cells. Cell Reprogram. 2016; 18(1): 37-47.
  10. Wan Y, Zhang Y, Zhou Z, Jia R, Meng L, Huang R, et al. Effect of potassium simplex optimization medium (KSOM) and embryo screening on the production of human lactoferrin transgenic cloned dairy goats. Afr J Biotechnol. 2013; 12(49): 6887-6893.
  11. Hajian M, Jafarpour F, Aghamiri SM, Varnosfaderani SR, Esfahani MH. Effects of ovary storage temperature and embryo vitrification on somatic cell nuclear transfer outcomes in goats. Reprod Fertil Dev. 2020; 32(4): 419-424.
  12. Wilmut I, Schnieke AE, McWhir J, Kind AJ, Campbell KH. Viable offspring derived from fetal and adult mammalian cells. Nature. 1997; 385(6619): 810-813.
  13. Cordova A, King WA, Mastromonaco GF. Choosing a culture me­dium for SCNT and iSCNT reconstructed embryos: from domestic to wildlife species. J Anim Sci Technol. 2017; 59: 24.
  14. Hosseini SM, Hajian M, Ostadhosseini S, Forouzanfar M, Abedi P, Jafarpour F, et al. Contrasting effects of G1. 2/G2. 2 and SOF1/SOF2 embryo culture media on pre-and post-implantation develop­ment of non-transgenic and transgenic cloned goat embryos. Re­prod Biomed Online. 2015; 31(3): 372-383.
  15. Hosseini SM, Moulavi F, Nasr-Esfahani MH. A novel method of so­matic cell nuclear transfer with minimum equipment. Methods Mol Biol. 2015; 1330: 169-188.
  16. Lan GC, Han D, Wu YG, Han ZB, Ma SF, Liu XY, et al. Effects of duration, concentration, and timing of ionomycin and 6-dimeth­ylaminopurine (6-DMAP) treatment on activation of goat oocytes. Mol Reprod Dev. 2005; 71(3): 380-388.
  17. McGraw S, Vigneault C, Sirard MA. Temporal expression of fac­tors involved in chromatin remodeling and in gene regulation dur­ing early bovine in vitro embryo development. Reproduction. 2007; 133(3): 597-608.
  18. Nielsen JMK, Wrenzycki C, Hyttel P, Poppicht F, Strøbech L. New IVF media affect blastocyst development and gene expression lev­els in in vitro produced bovine embryos. Reprod Fertil Dev. 2015; 27(1): 206-207.
  19. Penitente-Filho JM. Improved in vitro production systems for bo­vine embryos. CAB Reviews. 2015; 10(048): 1-4.
  20. Chiavarini M, Ostorero A, Naldini G, Fabiani R. Cancer risk in chil­dren and young adults (offspring) born after medically assisted re­production: a systematic review and meta-analysis. J Multidiscip Sci. 2019; 2(4): 430-448.
  21. Hargreave M, Jensen A, Hansen MK, Dehlendorff C, Winther JF, Schmiegelow K, et al. Association between fertility treatment and cancer risk in children. JAMA. 2019; 322(22): 2203-2210.
  22. Holm P, Booth PJ, Schmidt MH, Greve T, Callesen H. High bovine blastocyst development in a static in vitro production system using SOFaa medium supplemented with sodium citrate and myo-ino­sitol with or without serum-proteins. Theriogenology. 1999; 52(4): 683-700.
  23. HosseinNia P, Hajian M, Tahmoorespur M, Hosseini SM, Ostad­hosseini S, Nasiri MR, et al. Expression profile of developmentally important genes in preand peri-implantation goat embryos pro­duced in vitro. Int J Fertil Steril. 2016; 10(3): 310-319.
  24. HosseinNia P, Hajian M, Jafarpour F, Hosseini SM, Tahmoorespur M, Nasr-Esfahani MH. Dynamics of the expression of pluripotency and lineage specific genes in the pre and peri-implantation goat embryo. Cell J. 2019; 21(2): 194-203.
  25. Naddafpour A, Zadegan FG, Hajian M, Hosseini SM, Jafarpour F, Rahimi M, et al. Effects of abundances of OCT-4 mRNA transcript on goat pre-implantation embryonic development. Anim Reprod Sci. 2020; 215: 106286.
  26. Alberio R. Regulation of cell fate decisions in early mammalian em­bryos. Annu Rev Anim Biosci. 2020; 8: 377-393.
  27. Hajian M, Hosseini SM, Ostadhosseini S, Nasr-Esfahani MH. Targeting the transforming growth factor-β signaling during pre-implantation development in embryos of cattle, sheep and goats. Growth Factors. 2016; 34(3-4): 141-148.
  28. Moradi M, Riasi A, Ostadhosseini S, Hajian M, Hosseini M, Hos­seinnia P, et al. Expression profile of FGF receptors in preim­plantation ovine embryos and the effect of FGF2 and PD173074. Growth Factors. 2015; 33(5-6): 393-400.
  29. Morris SA, Guo Y, Zernicka-Goetz M. Developmental plasticity is bound by pluripotency and the Fgf and Wnt signaling pathways. Cell Rep. 2012; 2(4): 756-765.
  30. Denicol AC, Block J, Kelley DE, Pohler KG, Dobbs KB, Mortensen CJ, et al. The WNT signaling antagonist Dickkopf-1 directs lineage commitment and promotes survival of the preimplantation embryo. FASEB J. 2014; 28(9): 3975-3986.