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BOR - Papers in Press, published online ahead of print October 31, 2002.
Biol Reprod 2002, 10.1095/biolreprod.102.010090
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BIOLOGY OF REPRODUCTION 68, 1165–1169 (2003)
DOI: 10.1095/biolreprod.102.010090
© 2003 by the Society for the Study of Reproduction, Inc.


Embryo

Maintenance of the Inner Cell Mass in Human Blastocysts from Fragmented Embryos

Kate Hardy1,a,c, Jaroslav Starkb, and Robert M.L. Winstona

a Department of Reproductive Science and Medicine, Institute of Reproductive and Developmental Biology, The Wolfson and Weston Research Centre for Family Health, Imperial College, Hammersmith Hospital, London W12 ONN, United Kingdom b Department of Mathematics, University College London, London WC1E 6BT, United Kingdom c CoMPLEX (Centre for Mathematics and Physics in the Life Sciences and Experimental Biology), University College London, London WC1E 6BT, United Kingdom

The degree of fragmentation during early cleavage is universally used as an indicator of embryo quality during human in vitro fertilization treatment. Extensive fragmentation has been associated with reduced blastocyst formation and implantation. We examined the relationship between early fragmentation and subsequent allocation of cells to the trophectoderm and inner cell mass in the human blastocyst. We retrospectively analyzed data from 363 monospermic human embryos that exhibited varying degrees of fragmentation on Day 2. Embryos were cultured from Day 2 to Day 6 in Earle balanced salt solution with 1 mM glucose and human serum albumin. Rates of development and blastocyst formation were measured. The number of cells in the trophectoderm and inner cell mass and the incidence of apoptosis were assessed following differential labeling with polynucleotide-specific fluorochromes. Increasing fragmentation resulted in reduced blastocyst formation and lower blastocyst cell numbers. For minimal and moderate levels of fragmentation, the reduction in cell numbers was confined largely to the trophectoderm and a steady number of inner cell mass cells was maintained. However, with extensive fragmentation of more than 25%, cell numbers in both lineages were reduced in the few embryos that formed blastocysts. Apoptotic nuclei were present in both the trophectoderm and inner cell mass, with the lowest incidence in blastocysts that had developed from embryos with minor (5–10%) fragmentation. Paradoxically, higher levels of apoptosis were seen in embryos of excellent morphology, suggesting a possible role in regulation of cell number.

1 Correspondence: Kate Hardy, Department of Reproductive Science and Medicine, Institute of Reproductive and Developmental Biology, Imperial College, Hammersmith Hospital, Du Cane Road, London W12 ONN, U.K. FAX: 44 020 7594 2111; k.hardy{at}ic.ac.uk




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