Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published October 2001 | Published
Journal Article Open

Blastomeres arising from the first cleavage division have distinguishable fates in normal mouse development

Abstract

Two independent studies have recently suggested similar models in which the embryonic and abembryonic parts of the mouse blastocyst become separated already by the first cleavage division. However, no lineage tracing studies carried out so far on early embryos provide the support for such a hypothesis. Thus, to re-examine the fate of blastomeres of the two-cell mouse embryo, we have undertaken lineage tracing studies using a non-perturbing method. We show that two-cell stage blastomeres have a strong tendency to develop into cells that comprise either the embryonic or the abembryonic parts of the blastocyst. Moreover, the two-cell stage blastomere that is first to divide will preferentially contribute its progeny to the embryonic part. Nevertheless, we find that the blastocyst embryonic-abembryonic axis is not perfectly orthogonal to the first cleavage plane, but often shows some angular displacement from it. Consequently, there is a boundary zone adjacent to the interior margin of the blastocoel that is populated by cells derived from both earlier and later dividing blastomeres. The majority of cells that inhabit this boundary region are, however, derived from the later dividing two-cell stage blastomere that contributes predominantly to the abembryonic part of the blastocyst. Thus, at the two-cell stage it is already possible to predict which cell will contribute a greater proportion of its progeny to the abembryonic part of the blastocyst (region including the blastocyst cavity) and which to the embryonic part (region containing the inner cell mass) that will give rise to the embryo proper.

Additional Information

© 2001 The Company of Biologists. Accepted July 11, 2001. We acknowledge Chris Graham for his insightful suggestion of the need for careful lineage tracing in the preimplantation mouse embryo. We are grateful to David Glover for all his great help in preparation of this manuscript and discussions, to Nick Brown for his suggestion of non-invasive methods for cell labelling and to Peter Lawrence for the very helpful suggestion of dissociating blastocysts with trypsin to enable us to record the total number of cells per clone. This work was supported by grants from the Wellcome Trust and Human Frontier Science Program. M. Z.-G. is a Senior Research Fellow of the Lister Foundation for Preventive Medicine and a Stanley Elmore Fellow of Sidney Sussex College.

Attached Files

Published - 3739.full.pdf

Files

3739.full.pdf
Files (668.7 kB)
Name Size Download all
md5:9c966a8e99ccf3b094a286ef8cca9440
668.7 kB Preview Download

Additional details

Created:
August 19, 2023
Modified:
October 20, 2023