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Analysis of cellular behavior and cytoskeletal dynamics reveal a constriction mechanism driving optic cup morphogenesis.细胞行为和细胞骨架动力学分析揭示了一种驱动视杯形态发生的收缩机制。
Elife. 2016 Oct 31;5:e15797. doi: 10.7554/eLife.15797.
2
RhoA GTPase inhibition organizes contraction during epithelial morphogenesis.RhoA GTP酶抑制在上皮形态发生过程中组织收缩。
J Cell Biol. 2016 Aug 29;214(5):603-17. doi: 10.1083/jcb.201603077. Epub 2016 Aug 22.
3
Three-dimensional vertex model for simulating multicellular morphogenesis.用于模拟多细胞形态发生的三维顶点模型。
Biophys Physicobiol. 2015 Aug 18;12:13-20. doi: 10.2142/biophysico.12.0_13. eCollection 2015.
4
Shape Transformations of Epithelial Shells.上皮壳的形状转变
Biophys J. 2016 Apr 12;110(7):1670-1678. doi: 10.1016/j.bpj.2016.03.009.
5
Invagination of Ectodermal Placodes Is Driven by Cell Intercalation-Mediated Contraction of the Suprabasal Tissue Canopy.外胚层基板的内陷是由基底层上方组织冠层的细胞插入介导收缩驱动的。
PLoS Biol. 2016 Mar 9;14(3):e1002405. doi: 10.1371/journal.pbio.1002405. eCollection 2016 Mar.
6
Interface Contractility between Differently Fated Cells Drives Cell Elimination and Cyst Formation.不同命运细胞之间的界面收缩性驱动细胞消除和囊肿形成。
Curr Biol. 2016 Mar 7;26(5):563-74. doi: 10.1016/j.cub.2015.12.063. Epub 2016 Feb 4.
7
Quantitative Morphology of Epithelial Folds.上皮皱襞的定量形态学
Biophys J. 2016 Jan 5;110(1):269-77. doi: 10.1016/j.bpj.2015.11.024.
8
How do changes at the cell level affect the mechanical properties of epithelial monolayers?细胞水平的变化如何影响上皮单层的力学特性?
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Mechanisms of cell height changes that mediate epithelial invagination.介导上皮内陷的细胞高度变化机制。
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由顶端或基底外侧调节驱动的上皮折叠:几何特征、力学推断及边界效应

Epithelial Folding Driven by Apical or Basal-Lateral Modulation: Geometric Features, Mechanical Inference, and Boundary Effects.

作者信息

Wen Fu-Lai, Wang Yu-Chiun, Shibata Tatsuo

机构信息

Laboratory for Physical Biology, RIKEN Quantitative Biology Center, Kobe, Hyogo, Japan.

Laboratory for Epithelial Morphogenesis, RIKEN Center for Developmental Biology, Kobe, Hyogo, Japan.

出版信息

Biophys J. 2017 Jun 20;112(12):2683-2695. doi: 10.1016/j.bpj.2017.05.012.

DOI:10.1016/j.bpj.2017.05.012
PMID:28636924
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5479116/
Abstract

During embryonic development, epithelial sheets fold into complex structures required for tissue and organ functions. Although substantial efforts have been devoted to identifying molecular mechanisms underlying epithelial folding, far less is understood about how forces deform individual cells to sculpt the overall sheet morphology. Here we describe a simple and general theoretical model for the autonomous folding of monolayered epithelial sheets. We show that active modulation of intracellular mechanics along the basal-lateral as well as the apical surfaces is capable of inducing fold formation in the absence of buckling instability. Apical modulation sculpts epithelia into shallow and V-shaped folds, whereas basal-lateral modulation generates deep and U-shaped folds. These characteristic tissue shapes remain unchanged when subject to mechanical perturbations from the surroundings, illustrating that the autonomous folding is robust against environmental variabilities. At the cellular scale, how cells change shape depends on their initial aspect ratios and the modulation mechanisms. Such cell deformation characteristics are verified via experimental measurements for a canonical folding process driven by apical modulation, indicating that our theory could be used to infer the underlying folding mechanisms based on experimental data. The mechanical principles revealed in our model could potentially guide future studies on epithelial folding in diverse systems.

摘要

在胚胎发育过程中,上皮细胞层会折叠成组织和器官功能所需的复杂结构。尽管人们已投入大量精力来确定上皮细胞折叠背后的分子机制,但对于力如何使单个细胞变形以塑造整体细胞层形态的了解却少得多。在此,我们描述了一种单层上皮细胞层自主折叠的简单通用理论模型。我们表明,沿基底外侧以及顶端表面对细胞内力学进行主动调节,能够在不存在屈曲不稳定性的情况下诱导褶皱形成。顶端调节将上皮细胞塑造为浅的V形褶皱,而基底外侧调节则产生深的U形褶皱。当受到来自周围环境的机械扰动时,这些特征性的组织形状保持不变,这表明自主折叠对环境变化具有鲁棒性。在细胞尺度上,细胞如何改变形状取决于它们的初始纵横比和调节机制。通过对由顶端调节驱动的典型折叠过程进行实验测量,验证了这种细胞变形特征,这表明我们的理论可用于根据实验数据推断潜在的折叠机制。我们模型中揭示的力学原理可能会为未来不同系统中上皮细胞折叠的研究提供指导。