Viscous shear is a key force in Drosophila ventral furrow morphogenesis.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Development Pub Date : 2024-11-15 DOI:10.1242/dev.202892
Amanda Nicole Goldner, Mohamad Ibrahim Cheikh, Miriam Osterfield, Konstantin Doubrovinski
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引用次数: 0

Abstract

Ventral furrow (VF) formation in Drosophila melanogaster is an important model of epithelial folding. Previous models of VF formation require cell volume conservation to convert apically localized constriction forces into lateral cell elongation and tissue folding. Here, we have investigated embryonic morphogenesis in anillin knockdown (scra RNAi) embryos, where basal cell membranes fail to form and therefore cells can lose cytoplasmic volume through their basal side. Surprisingly, the mesoderm elongation and subsequent folding that comprise VF formation occurred essentially normally. We hypothesized that the effects of viscous shear may be sufficient to drive membrane elongation, providing effective volume conservation, and thus driving tissue folding. Since this hypothesis may not be possible to test experimentally, we turned to a computational approach. To test whether viscous shear is a dominant force for morphogenesis in vivo, we developed a 3D computational model incorporating both accurate cell and tissue geometry, and experimentally measured material parameters. Results from this model demonstrate that viscous shear generates sufficient force to drive cell elongation and tissue folding in vivo.

粘性剪切力是果蝇腹沟形态发生的关键力量。
黑腹果蝇腹侧沟(VF)的形成是上皮折叠的一个重要模型。以往的 VF 形成模型需要细胞体积守恒,才能将顶部局部的收缩力转化为横向细胞伸长和组织折叠。在这里,我们研究了anillin基因敲除(scra RNAi)胚胎的胚胎形态发生,在这种胚胎中,基底细胞膜无法形成,因此细胞可通过其基底侧失去细胞质体积。令人惊讶的是,中胚层的伸长和随后的折叠(包括 VF 的形成)基本正常。我们假设,粘性剪切力的影响可能足以驱动膜伸长,提供有效的体积守恒,从而驱动组织折叠。由于这一假设可能无法通过实验来验证,我们转而采用了计算方法。为了测试粘性剪切力是否是体内形态发生的主导力量,我们开发了一个三维计算模型,其中包含精确的细胞和组织几何形状以及实验测量的材料参数。该模型的结果表明,粘性剪切力产生了足够的力量来驱动体内细胞伸长和组织折叠。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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