Preimplantation Developmental Ability of Pig Embryos according to Embryonic Compaction Patterns

돼지수정란의 Compaction 양상에 따른 착상전 배발달 양상

  • 구덕본 (대구대학교 공과대학 생명공학과) ;
  • 민성훈 (대구대학교 공과대학 생명공학과) ;
  • 박흠대 (대구대학교 공과대학 생명공학과)
  • Received : 2010.06.15
  • Accepted : 2010.08.11
  • Published : 2010.09.30

Abstract

Embryonic compaction is essential for normal preimplantation development in mammals. The present study was to investigate the effects of compaction patterns on developmental competence of pig embryos. The proportion of blastocyst formation derived from compacted morula was higher than those of compacting and pre-compacting morula (P<0.01). Nuclei numbers of inner cell mass (ICM), trophectoderm (TE), and total of blastocysts derived from compacted group were also superior to those of compacting and pre-compacting groups (P<0.05). Then, compaction patterns, developmental ability and structural integrity were compared between mono- and poly-spermic embryos. The rate of compacted morula in mono-spermic embryos was higher than that of poly-spermic embryos (P<0.05). Especially, the rate of blastocyst formation derived from compacted embryos in mono-spermic embryo group was higher than that of poly-spermic embryo group (P<0.05), although no difference was detected between the two groups in the structural integrity. Finally, we confirmed that beta-catenin was differentially expressed according to compaction patterns in morula and blastocyst stage embryos. In conclusion, our results suggest that the compaction patterns during preimplantation development play a direct role in developmetal competence and quality of pig embryos.

Keywords

References

  1. Abeydeera LR and Day BN. 1997. Fertilization and subsequent development in vitro of pig oocytes inseminated in a modified tris-buffered medium with frozen-thawed ejaculated spermatozoa. BioI. Reprod. 57:729-734. https://doi.org/10.1095/biolreprod57.4.729
  2. Butz S and Larue L. 1995. Expression of catenins during mouse embryonic development and in adult tissues. Cell. Adhes. Commun. 3:337-352. https://doi.org/10.3109/15419069509081018
  3. Funahashi H and Day BN. 1993. Effects of the duration of exposure to hormone supplements on cytoplasmic maturation of pig oocytes in vitro. J. Reprod. Fertil. 98:179-185. https://doi.org/10.1530/jrf.0.0980179
  4. Giles JR and Foote RH. 1995. Rabbit blastocyst: Allocation of cells to the inner cell mass and trophectoderm. Mol. Reprod. Dev. 41:204-211. https://doi.org/10.1002/mrd.1080410211
  5. Han YM, Abeydeera LR, Kim JH, Moon HB, Cabot RA, Day BN and Prather RS. 1999a. Growth retardation of inner cell mass cells in polyspermic porcine embryos produced in vitro. BioI. Reprod. 60:1110-1113. https://doi.org/10.1095/biolreprod60.5.1110
  6. Han YM, Wang WH, Abeydeera LR, Petersen AL, Kim JH, Murphy C, Day BN and Prather RS. 1999b. Pronuclear location before the first cell division determines ploidy of polyspermic pig embryos. BioI. Reprod. 61:1340-1346. https://doi.org/10.1095/biolreprod61.5.1340
  7. Johnson MH and Ziomek CA. 1981. The foundation of two distinct cell lineages within the mouse morula. Cell 24:71-80. https://doi.org/10.1016/0092-8674(81)90502-X
  8. Jun T, Robert T, Katharine F, Brenda W, Tresa NW and Randall C. 2002. The neglected morula/compaction stage embryo transfer. Hum. Reprod. 17:1513-1518. https://doi.org/10.1093/humrep/17.6.1513
  9. Kim JS, Chae JI, Song BS, Lee KS, Choo YK, Chang KT, Park HD and Koo DB. 2010. Iloprost, a prostacyclin analogue, stimulates meiotic maturation and early embryonic development in pigs. Reprod. Fertil. Dev. 22:437-447. https://doi.org/10.1071/RD08287
  10. Machaty Z, Day BN and Prather RS. 1998. Development of early porcine embryos in vitro and in vivo. BioI. Reprod. 59:451-455. https://doi.org/10.1095/biolreprod59.2.451
  11. Miller JR and McClay DR. 1997. Characterization of the role of cadherin in regulating cell adhesion during sea urchin development. Dev. BioI. 192:323-339. https://doi.org/10.1006/dbio.1997.8740
  12. Moon RT and Kimelman D. 1998. From cortical rotation to organizer gene expression: toward a molecular explanation of axis specification in Xenopus. Bioessays 20:536-545. https://doi.org/10.1002/(SICI)1521-1878(199807)20:7<536::AID-BIES4>3.0.CO;2-I
  13. Nganvongpanit K, Muller H, Rings F, Gilles M, Jennen D, Holker M, Tholen E, Schellander K and Tesfaye D. 2006. Targeted suppression of E-cadherin gene expression in bovine preimplantation embryo by RNA interference technology using double-stranded RNA. Mol. Reprod. Dev. 73:153-163. https://doi.org/10.1002/mrd.20406
  14. Niwa K. 1993. Effectiveness of in vitro maturation and in vitro fertilization techniques in pigs. J. Reprod. Fertil. Suppl. 48:49-59.
  15. Pauken CM and Capco DG. 1999. Regulation of cell adhesion during embryonic compaction of mammalian embryos: Roles for PKC and beta-catenin. Mol. Reprod. Dev. 54:135-144. https://doi.org/10.1002/(SICI)1098-2795(199910)54:2<135::AID-MRD5>3.0.CO;2-A
  16. Petters RM and Wells KD. 1993. Culture of pig embryos. J. Reprod. Fertil. Suppl. 48:61-73.
  17. Prather RS, Boice ML, Gibson J, Hoffman KE and Parry TW. 1995. In vitro development of embryos from sinclair miniature pigs: A preliminary report. Theriogenology 43:1001-1007. https://doi.org/10.1016/0093-691X(95)00064-F
  18. Tam PP and Behringer RR. 1997. Mouse gastrulation: the formation of a mammalian body plan. Mech. Dev. 68:3-25. https://doi.org/10.1016/S0925-4773(97)00123-8
  19. Wang WH, Okuda K, Niwa K. 1991. In vitro penetration of pig oocytes matured in culture by frozen-thawed ejaculated spermatozoa. J. Reprod. Fertil. 93:491-499. https://doi.org/10.1530/jrf.0.0930491
  20. Winkel GK, Ferguson JE, Takeichi M and Nuccitelli R. 1990. Activation of protein kinase C triggers premature compaction in the four-cell stage mouse embryo. Dev. BioI. 138: 1-15. https://doi.org/10.1016/0012-1606(90)90171-E
  21. Yoshioka K, Suzuki C, Tanaka A, Anas IM and Iwamura S. 2002. Birth of piglets derived from porcine zygotes cultured in a chemically defmed medium. BioI. Reprod. 66:112-119. https://doi.org/10.1095/biolreprod66.1.112