The size of preimplantation mouse embryos was experimentally manipulated in order to examine the consequences for the allocation of cells to the two primary tissues, trophectoderm and inner cell mass (ICM). Half embryos were produced by the mechanical lysis of one cell at the two-cell stage and quad
Cell allocation in preimplantation mouse chimeras
✍ Scribed by Spindle, Akiko
- Book ID
- 102892727
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 539 KB
- Volume
- 219
- Category
- Article
- ISSN
- 0022-104X
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✦ Synopsis
Abstract
The mechanism of cell allocation in the preimplantation mouse chimera was studied in aggregation chimeras of 4‐ and 8‐cell stage embryos. To follow the fate of cells, some embryos were labeled by a 16‐h incubation (at the 2‐cell stage) with ^3^H‐thymidine. At the 4‐8‐cell stage both labeled and unlabeled embryos were treated with pronase to remove the zona pellucida and then aggregated in various combinations: one labeled 8‐cell and three unlabeled 4‐cell embryos (labeled 8‐cell chimeras); one labeled 4‐cell and three unlabeled 8‐cell embryos or two labeled 4‐cell and two unlabeled 8‐cell embryos (labeled 4‐cell chimeras). Autoradiography of air‐dried preparations of inner cell masses isolated from the chimeras at the blastocyst or late blastocyst stage by immunosurgery revealed that labeled 8‐cell embryos contributed a disproportionately large number (over 60%) of their descendant cells to the inner cell mass of labeled 8‐cell chimeras. By contrast, in labeled 4‐cell chimeras only 8% (with one labeled 4‐cell embryo) or 31% (with two labeled 4‐cell embryos) of inner cell mass cells were derived from the labeled embryos. These results suggest that cell allocation in preimplantation mouse chimeras is not a random process and that cells of embryos developing ahead of others are preferentially allocated to the inner cell mass.
📜 SIMILAR VOLUMES
Recent evidence suggests that the Ly-m11 alloantigen (Tada et al. 1980) is an allotypic determinant of mouse beta-2-microglobulin (B2m). In support of this are: (1) tight genetic linkage between the Ly-mll locus and the locus governing structural polymorphism of B2m (Michaelson 1981, Goding 1981),