A deformation gradient decomposition method for the analysis of the mechanics of morphogenesis

被引:47
|
作者
Munoz, Jose J.
Barrett, Kathy
Miodownik, Mark [1 ]
机构
[1] Kings Coll London, Div Engn, Mat Grp, London WC2R 2LS, England
[2] Univ Politecn Cataluna, Dept Appl Math 3, E-08028 Barcelona, Spain
[3] UCL, Dept Anat & Dev Biol, London W1N 8AA, England
[4] UCL, Dept Biochem & Mol Biol, London W1N 8AA, England
基金
英国生物技术与生命科学研究理事会;
关键词
invagination; Drosophila; finite elasticity; finite elements;
D O I
10.1016/j.jbiomech.2006.05.006
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A new finite element model is proposed for the analysis of the mechanical aspects of morphogenesis and tested on the biologically well studied gastrulation phenomenon, in particular ventral furrow invagination of the Drosophila melanogaster embryo. A set of mechanisms are introduced in the numerical model, which lead to the observed deformed shapes. We split the total deformation into two parts: an imposed active deformation, and an elastic deformation superimposed onto the latter. The active deformation simulates the effects of apical constriction and apico-basal elongation. These mechanisms are associated with known gene expressions and so in this way we attempt to bridge the well explored signalling pathways, and their associated phenotypes in a mechanical model. While the former have been studied in depth, much less can be said about the forces they produce and the mechanisms involved. From the numerical results, we are able to test different plausible mechanical hypotheses that generate the necessary folding observed in the invagination process. In particular, we conclude that only certain ratios between both modes (apical constriction and apico-basal elongation) can successfully reproduce the invagination process. The model also supports the idea that this invagination requires the contribution of several mechanisms, and that their redundancy provides the necessary robustness. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1372 / 1380
页数:9
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