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Clinically failed eggs as a source of normal human embryo stem cells.

TitleClinically failed eggs as a source of normal human embryo stem cells.
Publication TypeJournal Article
Year of Publication2009
Authorsde Sousa P, Gardner J, Sneddon S, Pells S, Tye BJorgensen, Dand P, Collins DM, Stewart K, Shaw L, Przyborski S, Cooke M, K McLaughlin J, Kimber SJ, Lieberman BA, Wilmut I, Brison DR
JournalStem Cell Res
Volume2
Issue3
Pagination188-97
Date Published2009 May
ISSN1876-7753
KeywordsBlastocyst, Chromosomes, Human, Embryonic Stem Cells, Gene Expression Profiling, Heterozygote, Humans, Zygote
Abstract

The promise of human embryo stem cells (hESCs) for regenerative medicine is offset by the ethical and practical challenges involved in sourcing eggs and embryos for this objective. In this study we sought to isolate an hESC line from clinically failed eggs, the usage of which would not conflict with donor interests to conceive. A total of 8 blastocysts were allocated for hESC derivation from a pool of 579 eggs whose fertilization had been clinically assessed to have occurred abnormally (i.e., three pronuclei) or failed (i.e., no pronuclei) following in vitro insemination or intracytoplasmic sperm injection (ICSI). The latter were subjected to a recovery intervention consisting of either reinsemination by ICSI or parthenogenetic stimulation. One hESC line (RCM1) was obtained from a failed-to-fertilize inseminated egg recovered by parthenogenetic activation. Standard in vitro and in vivo characterization revealed this line to possess all of the properties attributed to a normal euploid hESC line. Whole-genome single-nucleotide polymorphism analysis further revealed that the line was biparental, indicating that sperm penetration had occurred, although parthenogenetic stimulation was required for activation. Our results demonstrate the viability of an alternative strategy to generate normal hESC lines from clinically failed eggs, thereby further minimizing the potential to conflict with donor reproductive interest to conceive.

DOI10.1016/j.scr.2009.01.002
Alternate JournalStem Cell Res
PubMed ID19393594
Grant ListG0300484 / / Medical Research Council / United Kingdom
G0700092 / / Medical Research Council / United Kingdom
G0801057 / / Medical Research Council / United Kingdom
/ / Medical Research Council / United Kingdom