Origin of the ectoplacental cone and secondary giant cells in mouse blastocysts reconstituted from isolated trophoblast and inner cell mass

R. L. Gardner, Virginia E. Papaioannou, S. C. Barton

Development · 1973 · 259 citations · 16 references

DOIFull text

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Concepts

TL;DR

The study isolated inner cell mass and trophoblast tissues from mouse blastocysts, reconstituted embryos from these tissues, transferred them to pseudo‑pregnant recipients, and after early somite development dissected and GPI‑typed the embryo, membranes, and trophoblast while quantifying maternal decidual contamination. Results showed that the implanted trophoblast was almost entirely donor‑derived, the embryo plus membranes were largely ICM‑derived but also contained a substantial trophoblast component, and the data support a model in which the ICM limits trophoblast proliferation by suppressing giant cell differentiation rather than by contributing cells.

Abstract

ABSTRACT Inner cell mass (ICM) and trophoblast tissue were isolated from -day post-coitum mouse blastocysts that were homozygous for different electrophoretic variants of the enzyme glucose phosphate isomerase (GPI). Blastocysts were reconstituted from these tissues, transferred to pseudo-pregnant recipients and allowed to develop to the early somite stage. The embryo plus membranes and trophoblast were dissected and typed separately for GPI. Contamination of trophoblast with maternal decidual tissue was quantified. The trophoblast of the implanted embryos was almost exclusively of the trophoblastdonor GPI type. The embryos plus membranes were mainly of the ICM-donor type but most also showed a substantial proportion of trophoblast-donor type. It is argued that the ICM controls trophoblast proliferation by inhibiting giant cell transformation of adjacent trophoblast cells rather than through making a significant cellular contribution.

References

16