» Articles » PMID: 8342794

Onset of Gastrulation, Morphogenesis and Somitogenesis in Mouse Embryos Displaying Compensatory Growth

Overview
Date 1993 May 1
PMID 8342794
Citations 37
Authors
Affiliations
Soon will be listed here.
Abstract

This is a study on the ability of mouse embryos to compensate for a loss of cells and to develop with body parts of normal size and normal proportions during post-implantation development. Micro-manipulations were performed on 4-cell pre-implantation mouse embryos to reduce the number of cells by 25% (3/4 embryos) or 50% (2/4 embryos). Blastocysts developed from these embryos showed a preferential loss of inner cell mass population, and fewer of them formed viable embryos after implantation. The size of post-implantation 3/4 embryos was initially smaller than controls of the same gestational age, but compensatory growth, achieved by increasing cell numbers at above the normal rate and beyond the normal duration, took place between 6.5 and 11.5 days, resulting in a complete restoration of body size. During compensatory growth the 3/4 embryos rescheduled events of gastrulation and morphogenesis in keeping with cell number or body size appropriate for each developmental stage. The formation of the correct number of somites was accomplished by changing the rate of somite segmentation and by an adjustment of the size of individual somites and somitomeres proportional to the available amount of precursor tissues. Morphogenesis and pattern formation in embryos recovering from earlier cell losses are therefore regulated in accordance to tissue volume (or cell number) instead of chronological age or some intrinsic cellular clock.

Citing Articles

An explainable map of human gastruloid morphospace reveals gastrulation failure modes and predicts teratogens.

Rufo J, Qiu C, Han D, Baxter N, Daley G, Wilson M bioRxiv. 2024; .

PMID: 39386623 PMC: 11463602. DOI: 10.1101/2024.09.20.614192.


New findings on the orientation of the mouse anterior-posterior (A-P) axis before and during the initiation of gastrulation using a more refined embryo staging.

Hadjikypri X, Theofanous C, Christodoulidi A, Georgiades P Biochem Biophys Rep. 2024; 40:101817.

PMID: 39286290 PMC: 11402440. DOI: 10.1016/j.bbrep.2024.101817.


Inactivation of cytidine triphosphate synthase 1 prevents fatal auto-immunity in mice.

Soudais C, Schaus R, Bachelet C, Minet N, Mouasni S, Garcin C Nat Commun. 2024; 15(1):1982.

PMID: 38438357 PMC: 10912214. DOI: 10.1038/s41467-024-45805-y.


Progression of the pluripotent epiblast depends upon the NMD factor UPF2.

Chousal J, Sohni A, Vitting-Seerup K, Cho K, Kim M, Tan K Development. 2022; 149(21).

PMID: 36255229 PMC: 9687065. DOI: 10.1242/dev.200764.


Spatial transcriptomic profiling to identify mesoderm progenitors with precision genomic screening and functional confirmation.

Liu G, Yang G, Zhao G, Guo C, Zeng Y, Xue Y Cell Prolif. 2022; 55(10):e13298.

PMID: 35906841 PMC: 9528766. DOI: 10.1111/cpr.13298.


References
1.
Copp A . Interaction between inner cell mass and trophectoderm of the mouse blastocyst. I. A study of cellular proliferation. J Embryol Exp Morphol. 1978; 48:109-25. View

2.
Crossley P, LITTLE P . A cluster of related zinc finger protein genes is deleted in the mouse embryonic lethal mutation tw18. Proc Natl Acad Sci U S A. 1991; 88(18):7923-7. PMC: 52417. DOI: 10.1073/pnas.88.18.7923. View

3.
Poelmann R . Differential mitosis and degeneration patterns in relation to the alterations in the shape of the embryonic ectoderm of early post-implantation mouse embryos. J Embryol Exp Morphol. 1980; 55:33-51. View

4.
Tam P, Snow M . Proliferation and migration of primordial germ cells during compensatory growth in mouse embryos. J Embryol Exp Morphol. 1981; 64:133-47. View

5.
Burgoyne P, Tam P, Evans E . Retarded development of XO conceptuses during early pregnancy in the mouse. J Reprod Fertil. 1983; 68(2):387-93. DOI: 10.1530/jrf.0.0680387. View