Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Reproduction, Fertility and Development Reproduction, Fertility and Development Society
Vertebrate reproductive science and technology
RESEARCH ARTICLE

Rewards and risks of human embryo creation: a personal view

Henry J. Leese
+ Author Affiliations
- Author Affiliations

Department of Biology, University of York, PO Box 373, York YO10 5YW, UK. Email: hjl1@york.ac.uk

Reproduction, Fertility and Development 17(3) 387-391 https://doi.org/10.1071/RD04093
Submitted: 31 August 2004  Accepted: 1 November 2004   Published: 14 February 2005

Abstract

Understanding how a single cell, the fertilised egg, can develop into all the tissues in the body has been referred to as one of the two great problems facing biology; the other is how the brain works. To be working on the early human embryo is a reward in itself. To see such knowledge applied to improve the lives of infertile couples provides special rewards. There are considerable technical challenges in these activities due to the paucity of experimental material, particularly in the human. A major intellectual challenge is to understand the mechanisms that regulate early embryo development, especially the role of signal molecules intrinsic to the embryo and those that are maternally derived. Central to this issue are notions of embryo autonomy and plasticity; the extent to which the same genotype can give rise to different phenotypes in response to environmental perturbations and the need to discover how severe such changes have to be to induce irreversible changes that can compromise the health of the offspring. Research areas that could be fruitful include stress-induced causal effects, cell signalling and the concept of ‘quiet metabolism’. Managing assisted conception practices and their associated risks requires a regulatory framework to ensure the safety and efficacy of the new technologies. However, there is a danger of over-regulation, a cultural phenomenon characterised by a rise in audit and decline in trust. The challenge is to devise regulation in assisted reproduction technologies proportionate to the risks. The ultimate rewards will come from understanding how the human genome operates in functional terms. The ideal system in which to study this is the human blastocyst, an autonomous, functional group of mammalian cells.


Acknowledgments

I thank Daniel Brison and Jane Denton for most helpful comments and the UK Medical Research Council for their support of research on human embryo creation.


References

Bateson, P. , Barker, D. , Clutton-Brock, T. , Deb, D. , and D’Udine, B. , et al. (2004). Developmental plasticity and human health. Nature 430, 419–421.
Crossref | GoogleScholarGoogle Scholar | PubMed | HFEA (2003) ‘Avoiding Multiple Births: Deciding How Many Embryos to Transfer.’ (Human Fertilisation and Embryology Authority: London, UK.) Available at http://www.hfea.gov.uk/HFEAPublications/HFEAleaflets/Multiple%20births.pdf [Verified 16 December 2004].

Houghton, F. D. , Humpherson, P. G. , Hawkhead, J. A. , Hogg, J. E. , Balen, A. H. , Rutherford, A. J. , and Leese, H. J. (2002). Non-invasive amino acid turnover predicts human embryo developmental capacity. Hum. Reprod. 17, 999–1005. [Corrigenda (2003) Hum. Reprod. 18, 1756–1757].
Crossref | GoogleScholarGoogle Scholar | PubMed | Lodish H., Bert A., Matsudiaria P., Kaiser C. A., Kreiger M., Scott M. P., Zipursky S. L., and Darnell J. (2004) ‘Molecular Cell Biology.’ (W. H. Freeman: New York, NY, USA.)

Lu, D. P. , Chandrakanthan, V. , Cahana, A. , Ishii, S. , and O'Neill, C. (2004). Trophic signals acting via phosphatidylinositol-3 kinase are required for normal pre-implantation mouse embryo development. J. Cell Sci. 117, 1567–1576.
Crossref | GoogleScholarGoogle Scholar | PubMed | McLaren A. (1976) ‘Mammalian Chimaeras.’ (Cambridge University Press: Cambridge, UK.)

O’Neill O. (2003) ‘A Question of Trust.’ (Cambridge University Press: Cambridge, UK.)

Robinson, S. M. , and Barker, D. J. P. (2002). Coronary heart disease: a disorder of growth. Proc. Nutr. Soc. 61, 537–542.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Thompson, J. G. , Sherman, A. , Allen, N. , Mcgowan, L. , and Tervitt, H. (1998). Total protein content and protein synthesis within pre-elongation stage bovine embryos. Mol. Reprod. Dev. 50, 139–145.
PubMed |

Thompson, J. G. , Kind, K. L. , Roberts, C. T. , Robertson, S. A. , and Robinson, J. S. (2002). Epigenetic risks related to assisted reproductive technologies. Short and long-term consequences for the health of children conceived through assisted reproduction technology: more reason for caution. Hum. Reprod. 17, 2783–2786.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Turner, B. S. (1998). Risks, rights and regulation: an overview. Health Risk Soc. 3, 9–18.


Turner, K. , Goldstein, D. W. , and Rogers, A. W. (1992). Variation in the dry mass of mouse embryos throughout the preimplantation period. Hum. Reprod. 7, 112–116.
PubMed |

Winston, R. M. L. , and Hardy, K. (2002). Are we ignoring potential dangers of in vitro fertilization and related treatments? Nat. Cell Biol. 4, S14–S18.
Crossref | GoogleScholarGoogle Scholar | PubMed |