| Literature DB >> 28305692 |
Alan H Handyside1, Susan Hunter1.
Abstract
The numbers of cells in the trophectoderm (TE) and inner cell mass (ICM) of mouse blastocysts were counted by differentially labelling their nuclei with two polynucleotide-specific fluorochromes. Blastocysts recovered from the uterus at intervals between their formation early on Day 4 to the initial stages of implantation on day 5 were analysed. TE cell number increase was initially rapid, indicating some synchronisation of the sixth division, but slowed down progressively and plateaued on Day 5, possibly due to the onset of primary giant cell formation. ICM cell number increase was slower than the corresponding TE cells. As a result, TE cell number more than quadrupled, whereas ICM cell number only doubled over this period. Although the mitotic index of both populations of cells fell steadily, there was no significant difference between them. The decline in the proportion of ICM cells, therefore, is likely to be due to cell death, first detected in early blastocysts and predominantly located in the ICM. In addition, however, a contribution of ICM cells to the overlying polar TE cannot be excluded.Entities:
Keywords: Cell death; Cleavage; Inner cell mass; Mouse blastocyst; Trophectoderm
Year: 1986 PMID: 28305692 DOI: 10.1007/BF00375893
Source DB: PubMed Journal: Rouxs Arch Dev Biol ISSN: 0930-035X