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Biology of Reproduction 63, 1413-1420 (2000)
© 2000 Society for the Study of Reproduction, Inc.


Articles

Anti-Apoptotic Action of Insulin-Like Growth Factor-I During Human Preimplantation Embryo Development

Sophie Spanosb,c, David L. Beckerc, Robert M.L. Winstonc, and Kate Hardyc

b Department of Reproductive Science and Medicine, Division of Paediatrics, Obstetrics and Gynaecology, Imperial College School of Medicine, Hammersmith Hospital, London, W12 ONN, United Kingdom c Department of Anatomy and Developmental Biology, University College London, London WC1 6BT, United Kingdom

Insulin-like growth factor I (IGF-I) has been shown to increase the proportion of embryos forming blastocysts and the number of inner cell mass cells in human and other mammalian preimplantation embryos. Here we examined whether the increased cell number resulted from increased cell division or decreased cell death.

Normally fertilized, Day 2 human embryos of good morphology were cultured to Day 6 in glucose-free Earle's balanced salt solution supplemented with 1 mM glutamine, with (n = 42) and without (n = 45) 1.7 nM IGF-I. Apoptotic cells in Day 6 blastocysts were identified using terminal deoxynucleotidyl dUTP terminal transferase (TUNEL) labeling to detect DNA fragmentation and 4’-6-diamidino-2-phenylindole (DAPI) counterstain to evaluate nuclear morphology. The number of nuclei and extent of DNA and nuclear fragmentation was assessed using laser scanning confocal microscopy.

IGF-I significantly increased the proportion of embryos developing to the blastocyst stage from 49% (control) to 74% (+IGF-I) (P < 0.05). IGF-I also significantly decreased the mean proportion of apoptotic nuclei from 16.3 ± 2.9% (–IGF-I) to 8.7 ± 1.4% (+IGF-I) (P < 0.05). The total number of cells remained similar between both groups (61.7 ± 4.6 with IGF-I; 54.5 ± 5.1 without IGF-I). The increased number of blastocysts combined with reduced cell death suggests that IGF-I is rescuing embryos in vitro which would otherwise arrest and acting as a survival factor during preimplantation human development.

First decision: 1 May 2000.

1 Correspondence: Sophie Spanos, Dept. of Reproductive Science and Medicine, Division of Paediatrics, Obstetrics and Gynaecology, Imperial College School of Medicine, Hammersmith Hospital, Du Cane Rd., London, W12 ONN, UK. FAX: 4420 8383 2381; s.spanos{at}ic.ac.uk




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