Four-cell stage mouse blastomeres have different developmental properties

Author:

Piotrowska-Nitsche Karolina12,Perea-Gomez Aitana13,Haraguchi Seiki14,Zernicka-Goetz Magdalena1

Affiliation:

1. Wellcome Trust/Cancer Research UK Gurdon Institute and Department of Genetics,Tennis Court Road, Cambridge CB2 1QR, UK

2. Department of Experimental Embryology, Polish Academy of Science, Jastrzebiec 05-552, Poland

3. Développement des Vertébrés, Institut Jacques Monod,UMR7592 CNRS Universités Paris 6, 7. 2, place Jussieu, 75005 Paris,France

4. Department of Microbiology, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan

Abstract

Blastomeres of the early mouse embryo are thought to be equivalent in their developmental properties at least until the eight-cell stage. However, the experiments that have led to this conclusion could not have taken into account either the spatial origin of individual blastomeres or the spatial allocation and fate of their progeny. We have therefore readdressed this issue having defined cell lineages in mouse embryos undergoing different patterns of cleavage in their second division cycle. This has enabled us to identify a major group of embryos in which we can predict not only the spatial origin of each given four-cell blastomeres, but also which region of the blastocyst is most likely to be occupied by its progeny. We show that a pattern of second cleavage divisions in which a meridional division is followed by one that is equatorial or oblique allows us to identify blastomeres that differ in their fate and in their developmental properties both from each other and from their cousins. We find that one of these four-cell stage blastomeres that inherits some vegetal membrane marked in the previous cleavage cycle tends to contribute to mural trophectoderm. The progeny of its sister tend to donate cells to part of the ICM lining the blastocyst cavity and its associated trophectoderm. Chimaeras made entirely of these equatorially or obliquely derived blastomeres show developmental abnormalities in both late preimplantation and early postimplantation development. By contrast, chimaeras made from four-cell stage blastomeres from early meridional divisions develop normally. The developmental defects of chimaeras made from the most vegetal blastomeres that result from later second cleavages are the most severe and following transplantation into foster mothers they fail to develop to term. However, when such individual four-cell blastomeres are surrounded by blastomeres from random positions, they are able to contribute to all embryonic lineages. In conclusion, this study shows that while all four-cell blastomeres can have full developmental potential, they differ in their individual developmental properties according to their origin in the embryo from as early as the four-cell stage.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

Reference32 articles.

1. Belo, J. A., Bouwmeester, T., Leyns, L., Kertesz, N., Gallo, M.,Follettie, M. and de Robertis, E. M. (1997). Cerberus-like is a secreted factor with neutralizing activity expressed in the anterior primitive endoderm of the mouse gastrula. Mech. Dev.68, 45-57.

2. Ciemerych, M. A., Mesnard, D. and Zernicka-Goetz, M.(2000). Animal and vegetal poles of the mouse egg predict the polarity of the embryonic axis yet are nonessential for development. Development127,3467-3474.

3. Crossley, P. H. and Martin, G. R. (1995). The mouse Fgf8 gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo. Development2,439-451.

4. Fujimori, T., Kurotaki, Y., Miyazaki, J. I. and Nabeshima, Y. I. (2003). Analysis of cell lineage in two- and four-cell mouse embryos. Development21,5113-5122.

5. Gardner, R. L. (1997). The early blastocyst is bilaterally symmetrical and its axis of symmetry is aligned with the animal-vegetal axis of the zygote in the mouse. Development124,289-301.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3