Restricted distribution of tetraploid cells in mouse tetraploid ↔ diploid chimaeras

108Citations
Citations of this article
20Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Tetraploid mouse embryos were produced by electrofusion at the 2-cell stage, cultured overnight, and aggregated with normal diploid embryos to produce tetraploid ↔ diploid (4n ↔ 2n) chimaeric conceptuses. At 7 1/2 days the 4n ↔ 2n chimaeras were usually smaller and developmentally retarded compared to control diploid ↔ diploid chimaeras. At 12 1/2 days the 4n ↔ 2n chimaeras had heavier placentas but there was no significant difference in fetal size. Tetraploid cells showed a restricted tissue distribution at both developmental stages studied: 4n cells were commonly present in both the primitive endoderm and the trophectoderm lineages but they rarely contributed to the primitive ectoderm lineage. The overall similarity in the distribution of tetraploid cells at 7 1/2 and 12 1/2 days implies that whatever causes the restricted tissue distribution operates largely before 7 1/2 days. There was no evidence for excessive embryonic losses of 4n ↔ 2n chimaeras. So, if the restricted distribution of 4n cells was a result of cell selection, the mechanism is more likely to involve loss of 4n cells from the primitive ectoderm early in development rather than selective death of conceptuses with tetraploid cells in this lineage. Alternatively, 4n cells may be preferentially allocated to the trophectoderm and primitive endoderm rather than the primitive ectoderm layer at the blastocyst stage. © 1995 Academic Press, Inc.

Cite

CITATION STYLE

APA

James, R. M., Klerkx, A. H. E. M., Keighren, M., Flockhart, J. H., & West, J. D. (1995). Restricted distribution of tetraploid cells in mouse tetraploid ↔ diploid chimaeras. Developmental Biology, 167(1), 213–226. https://doi.org/10.1006/dbio.1995.1018

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free