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Volume 2, No 3 May/June 2001
Fertilizable oocytes reconstructed from patient’s somatic cell nuclei and donor ooplasts
J Tesarik1, ZP Nagy, M Sousa2, C Mendoza3, R Abdelmassih Clinic and Research Centre for Human Reproduction Roger Abdelmassih, São Paulo, Brasil 1Permanent address: Laboratoire d’Eylau, 55 rue Saint-Didier, 75116 Paris, France
Correspondence: fax +34 958 265043; e-mail: cmendoza@ugr.es 2Permanent address: Laboratory of Cell Biology, Institute of Biomedical Sciences, University of Porto, Largo Prof. Abel Salazar 2, Porto, Portugal 3Permanent address: MAR & Gen, Molecular Assisted Reproduction & Genetics, Gracia 36, 18002 Granada, Spain
The only assisted reproduction treatment now available for women with ovarian failure or irreparable oocyte defects is oocyte donation. However, some women experience psychological barriers against the recourse to donor oocytes, related to the lack of contribution of their proper genes to the progeny. A pilot study in humans is reported suggesting that this problem may be overcome by the development of techniques for haploidization of somatic cell nuclei, allowing the formation of new oocytes bearing the complete nuclear genome of the patient. Somatic cell nuclei were obtained from cumulus cells of a patient who failed to produce fertilizable oocytes and transferred into enucleated oocytes (ooplasts) from a donor. Out of six ooplasts injected with the somatic cell nuclei and fertilized with spermatozoa from the patient’s husband, signs of haploidization were detected in three oocytes, two of which subsequently started embryonic development and were cryopreserved for eventual future transfer to the genetic mother. These data show that human oocytes can be used for both reprogramming and haploidization of somatic cell nuclei, allowing reconstruction of oocytes genetically identical to their own for patients without, or with seriously disturbed, ovarian function.
Reproductive BioMedicine Online 2001 Vol. 2, No. 3 160-164
Keywords: haploidization, oocyte donation, oocyte reconstruction, ovarian failure, somatic cell
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