Skip to main content
Log in

Effects of different states of sheep fetal fibroblasts as donor cells on the early development in vitro of reconstructed sheep embryos

  • Published:
Science in China Series C: Life Sciences Aims and scope Submit manuscript

Abstract

To investigate the effects of different states of donor cells on the development of reconstructed sheep embryos, we designed five treatments of donor cells, including cell passage, cell size, serum starvation, colchicine treatment and gene transfection. Results are as follows: (I) Compared with 16–18 passage cells, the morula/blastocyst rate of 5–7 passage cells as donor nuclei was significantly higher (17.3% vs. 4.9%, P<0.05), suggesting the advantage of short-time cultured cells in supporting the development of reconstructed embryos. (II) The mourla/blastocyst rate of reconstructed embryos derived from medium cells (15–25 μm) as donor nuclei was higher than that from large cells (25–33 μm) and small cells (8–15 μm)(20.0% vs. 8.0%, 9.7%), indicating that reconstructed embryos from medium cells had a greater potentiality to develop into morula/blastocysts than those from small or large ones. (III) The morula/blastocyst rate of reconstructed embryos from donor cells of SS (serum starvation) was lower than that from donor cells of NSS (non-serum starvation), but no significant difference was detected between SS and NSS(11.8% vs. 18.6%, P>0.05). (IV) Fetal fibroblasts treated with 0.05 μmol/L colchicine exhibited a higher morula/blastocyst rate of reconstructed embryos than those treated with 0.10 μmol/L colchicine and untreated ones (27.5% vs. 12.1%, 17.1%), however, no significant difference among the three treatments was detected (P>0.05). (V) The morula/blastocyst rate of reconstructed embryos from fetal fibroblasts transfected with GFP gene only was 3.1%, significantly lower than that from non-transgenic cells (3.1% vs. 20.4%, P<0.05). In conclusion, our results demonstrated that fetal fibroblasts of fewer passages, medium size could ensure a higher morula/blastocyst rate of reconstructed embryos. Serum starvation of donor cells might be unnecessary to the development of reconstructed embryos. Donor cells treated with 0.05 μmol/L colchicine could facilitate the development of reconstructed embryos. Additionally, as cells transfected with GFP gene were used as donor nuclei, adverse effect on the development of reconstructed embryos was observed. Therefore, the developmental efficiency of reconstructed embryos could be improved if proper treatments to donor cells were used.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Willmut I, Schnieke A E, McWhir J, et al. Viable offspring derived from fetal and adult mammalian cells. Nature, 1997, 385: 810–813

    Article  Google Scholar 

  2. Baguisi A, Behboodi E, Melican D T, et al. Production of goat by somatic cell nuclear transfer. Nature Biotech, 1999, 17: 456–461

    Article  CAS  Google Scholar 

  3. Wakayama T, Rerry A C F, Zuccotti M, et al. Full-term development of mice from enucleated oocytes injected with cumulus cell nuclei. Nature, 1998, 392(23): 369–374

    Google Scholar 

  4. Kato Y, Tani T, Sotomaru Y, et al. Eight calves cloned from somatic cells of a single adult. Science, 1998, 282: 1975–1976

    Article  Google Scholar 

  5. Onishi A, Iwamoto M, Akita T, et al. Pig cloning by microinjection of fetal fibroblast nuclei. Science, 2000, 289: 2095–2097

    Article  Google Scholar 

  6. Galli C, Lagutina I, Crotti G, et al. Pregnancy: a cloned horse born to its dam twin. Nature, 2003, 424: 635.

    Article  PubMed  CAS  Google Scholar 

  7. Woods G L, White K L, Vanderwall D K, et al. A mule cloned from fetal cells by nuclear transfer. Science, 2003, 301(5636): 1063.

    Article  PubMed  CAS  Google Scholar 

  8. Shin T, Kraemer D, Pryor J, et al. A cat cloned by nuclear transplantation. Nature, 2002, 415: 859

    Article  PubMed  CAS  Google Scholar 

  9. Chesne P, Adenot P G, Viglietta C, et al. Cloned rabbits produced by nuclear transfer from adult somatic cells. Nat Biotechnol, 2002, 20(4): 366–369

    Article  PubMed  CAS  Google Scholar 

  10. Zhou Q, Renard J P, Le Friec G, et al. Generation of fertile cloned rats by regulating oocyte activation. Science, 2003, 302: 1179

    Article  PubMed  CAS  Google Scholar 

  11. Lee B C, Kim M K, Jang G, et al. Dogs cloned from adult somatic cells. Nature, 2005, 436(7051): 641

    Article  PubMed  CAS  Google Scholar 

  12. Colman A. Somatic cell nuclear transfer in mammals: Progress and applications. Cloning, 2000, 1: 185–200

    Article  CAS  Google Scholar 

  13. Oikawa T, Numabe T, Sunoda T, et al. Production of somatic cell clone calves from cumulus cell of a 20 year old Japanese black cow. Theriogenology, 2000, 53: 236 (abstract)

    Google Scholar 

  14. Wells D N, Misica P M, Tervit H R. Production of cloned calves following nuclear transfer with cultured adult mural granulose cell. Biol Reprod, 1999, 60: 996–1005

    Article  PubMed  CAS  Google Scholar 

  15. Shiga K, Fujita T, Hirose K, et al. Production of calves by transfer of nuclei from cultured somatic cells obtained from Japanese black bulls. Theriogenology, 1999, 38: 897–904

    Google Scholar 

  16. Ogura A, Inoue K, Ogonuki N. et al. Production of male cloned mice from fresh cultured and cryopreserved immature sertoli cells. Biol Reprod, 2000, 62: 1579–1584

    Article  PubMed  CAS  Google Scholar 

  17. Cibelli J B, Stice S L, Golueke P J, et al. Cloned transgenic calves produced from nonquiescent fetal fibroblasts. Science, 1998, 289: 1256–1258

    Article  Google Scholar 

  18. Schnieke A E, kind A J, Ritchie W A, et al. Human factor IX transgenic sheep produced by transfer of nuclei from transfected fetal fibroblasts. Science, 1997, 278: 2130–2133.

    Article  PubMed  CAS  Google Scholar 

  19. Zakhartchenko V, Durcova Hills G, Stojkovic M, et al. Effects of serum starvation and recloning on the efficiency of nuclear transfer using bovine fetal fibroblasts. J Reprod Fertil, 1999, 115(2): 325–331

    Article  PubMed  CAS  Google Scholar 

  20. Lai L X, Park K W, Cheong H T, et al. Transgenic pig expressing the enhanced green fluorescent protein produced by nuclear transfer using colchicines-treated fibroblasts as donor cells. Mol Reprod Dev, 2002, 62(3): 300–306

    Article  PubMed  CAS  Google Scholar 

  21. Reggio B C, James A N, Green H L, et al. Cloned transgenic offspring regulating from somatic cell nuclear transfer in the goat: oocytes derived from both follicle-stimulating hormone stimulated and non-stimulated abattoir-derived ovaries. Biol Reprod, 2001, 65: 1528–1533

    Article  PubMed  CAS  Google Scholar 

  22. Kubota C, Yamakuchi H, Todorki J, et al. Six cloned calves produced from adult fibroblast cells after long-term culture. Proc Natl Acad Sci USA, 2000, 97(3): 990–995

    Article  PubMed  CAS  Google Scholar 

  23. Prather R S. Cloning. Pigs is pigs. Science, 2000, 289: 1886–1887

    Article  PubMed  CAS  Google Scholar 

  24. Gong G, Dai Y, Fan B, et al. Birth of calves expressing the enhanced green fluorescent protein after transfer of fresh or vitrified/thawed blastocysts produced by somatic cell nuclear transfer. Mol Reprod Dev, 2004, 69: 278–288

    Article  PubMed  CAS  Google Scholar 

  25. E Z. Tissue Culture and Molecular Biotechnology (in Chinese). Beijing: Beijing Press, 1994

    Google Scholar 

  26. Andrew C, Boqiest, Billy N, et al. Flow cytometric cell analyses of cultured fetal fibroblast cells. Biol Reprod, 1999, 60: 1013–1019

    Article  Google Scholar 

  27. Mohamed Nour M S, Ikeda K, Takahashi Y. Bovine nuclear transfer using cumulus cells derived from serum-starved and confluent cultures. J Reprod Dev, 2000, 46: 85–92.

    Article  Google Scholar 

  28. Wells D N, Misica P M, Day A M, et al. Production of cloned lambs from an established embryonic cell line: a comparison between in vivo and in vitro-matured cytoplasts. Biol Reprod, 1997, 57: 385–393.

    Article  PubMed  CAS  Google Scholar 

  29. Campbell K H S, Ritchie W A, Wilmut I. Nuclear-cytoplasmic interactions during the first cell cycle of nuclear transfer reconstructed bovine embryos: implication for deoxyribonucleic acid replication and development. Biol Reprod, 1993, 49: 932–942

    Article  Google Scholar 

  30. Campbell K H S, McWhir J, Ritchie W A, et al. Sheep cloned by nuclear transfer from a cultured cell line. Nature, 1996b, 380: 64–66

    Article  PubMed  CAS  Google Scholar 

  31. Keefer C L, Keyston R, Lazaris A, et al. Production of cloned goats after nuclear transfer using adult somatic cells. Biol Reprod, 2002, 66: 199–203

    Article  PubMed  CAS  Google Scholar 

  32. Hill J R, Winger Q A, Long C R, et al. Development rates of male bovine nuclear transfer embryos derived from adult and fetal cells. Biol Reprod, 2000, 62: 1135–1140

    Article  PubMed  CAS  Google Scholar 

  33. Vignon X, LeBourshis D, Chesne P, et al. Development of bovine nuclear transfer embryos reconstituted with quiescent and proliferative skin fibroblasts. Theriogenology, 1999, 51: 216 (abstract)

    Article  Google Scholar 

  34. Hyun S, Lee G, Kim D, et al. Production of nuclear transfer-derived piglets using porcine fetal fibroblasted with the enhanced green fluorescent protein. Biol Reprod, 2003, 69: 1060–1068

    Article  PubMed  CAS  Google Scholar 

  35. Edwards J L, Dorado C M, Wilson T J, et al. Development of cloned embryos reconstructed with serum fed or serum starved adult granulosa cells. Theriogenology, 2001, 55: 265

    Article  Google Scholar 

  36. Kues W A, Anger M, Carnwath J W, et al. Cell cycle synchronization of porcine fetal fibroblasts: Effects of serum deprivation and reversible cell cycle inhibitors. Biol Reprod, 2000, 62: 412–419

    Article  PubMed  CAS  Google Scholar 

  37. Liu L, Dai Y, Moor R M. Nuclear transfer in sheep embryos: the effect of cell-cycle coordination between nucleus and cytoplasm and the use of in vitro mature oocytes. Mol Reprod Dev, 1997, 47: 255–264

    Article  PubMed  CAS  Google Scholar 

  38. Zhou Q, Jouneau A, Brochard V, et al. Developmental potential of mouse embryos reconstructed from metaphase embryonic stem cell nuclei. Biol Reprod, 2001, 65: 412–419

    PubMed  CAS  Google Scholar 

  39. Amano T, Tani T, Kato Y, et al. Mouse cloned from embryonic stem (ES) cells synchronized in metaphase with nocodazole. J Exp Zool, 2001, 289: 139–145

    Article  PubMed  CAS  Google Scholar 

  40. Guo G Q, Zhen G C. Study on molecule biology characters of GFP in viable cell. Research and Development of World Science and Technology (in Chinese). 1998, 1: 70–75

    Google Scholar 

  41. Park K W, Cheong H T, Lai L, et al. Production of nuclear transfer-derived swine that express the enhanced green fluorescent protein. Anim Biotechnol, 2001, 12: 173–181

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Lian ZhengXing or Wu ChangXin.

Additional information

Supported by the National Key Basic Research ‘973’ Program of China (Grant No. 2006CB102100) and Project of Agricultural Structure Adjustment of China (Grant No. 05-07-04B)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wang, H., Ao, H., Pan, Q. et al. Effects of different states of sheep fetal fibroblasts as donor cells on the early development in vitro of reconstructed sheep embryos. SCI CHINA SER C 50, 178–185 (2007). https://doi.org/10.1007/s11427-007-0013-5

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11427-007-0013-5

Keywords

Navigation