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本文引用的文献

1
Planar Differential Growth Rates Initiate Precise Fold Positions in Complex Epithelia.平面差动生长速率在复杂上皮组织中引发精确的褶皱位置。
Dev Cell. 2019 Nov 4;51(3):299-312.e4. doi: 10.1016/j.devcel.2019.09.009. Epub 2019 Oct 10.
2
Shaping of a three-dimensional carnivorous trap through modulation of a planar growth mechanism.通过调节平面生长机制来塑造三维肉食陷阱。
PLoS Biol. 2019 Oct 10;17(10):e3000427. doi: 10.1371/journal.pbio.3000427. eCollection 2019 Oct.
3
Structural Redundancy in Supracellular Actomyosin Networks Enables Robust Tissue Folding.细胞外肌动蛋白网络的结构冗余使组织能够稳健折叠。
Dev Cell. 2019 Sep 9;50(5):586-598.e3. doi: 10.1016/j.devcel.2019.06.015. Epub 2019 Jul 25.
4
Understanding the mechanical link between oriented cell division and cerebellar morphogenesis.理解定向细胞分裂和小脑形态发生之间的机械联系。
Soft Matter. 2019 Mar 6;15(10):2204-2215. doi: 10.1039/c8sm02231c.
5
Tissue curvature and apicobasal mechanical tension imbalance instruct cancer morphogenesis.组织弯曲和顶端基底机械张力失衡指导癌症形态发生。
Nature. 2019 Feb;566(7742):126-130. doi: 10.1038/s41586-019-0891-2. Epub 2019 Jan 30.
6
Differential lateral and basal tension drive folding of Drosophila wing discs through two distinct mechanisms.差异的侧向和基底张力通过两种不同的机制驱动果蝇翅盘的折叠。
Nat Commun. 2018 Nov 5;9(1):4620. doi: 10.1038/s41467-018-06497-3.
7
Basal epithelial tissue folding is mediated by differential regulation of microtubules.基底上皮组织折叠是由微管的差异调节介导的。
Development. 2018 Nov 19;145(22):dev167031. doi: 10.1242/dev.167031.
8
Basal constriction during midbrain-hindbrain boundary morphogenesis is mediated by Wnt5b and focal adhesion kinase.中脑-后脑边界形态发生过程中的基底收缩由Wnt5b和粘着斑激酶介导。
Biol Open. 2018 Nov 13;7(11):bio034520. doi: 10.1242/bio.034520.
9
How Cells Fold the Cerebral Cortex.细胞如何折叠大脑皮层。
J Neurosci. 2018 Jan 24;38(4):776-783. doi: 10.1523/JNEUROSCI.1106-17.2017.
10
Engineered Tissue Folding by Mechanical Compaction of the Mesenchyme.工程化组织折叠通过间质的机械压实。
Dev Cell. 2018 Jan 22;44(2):165-178.e6. doi: 10.1016/j.devcel.2017.12.004. Epub 2017 Dec 28.

关于折叠形态发生的力学问题

On folding morphogenesis, a mechanical problem.

机构信息

MRC Laboratory for Molecular Cell Biology, University College London, Gower Street, London WC1E 6BT, UK.

Institute for the Physics of Living Systems, University College London, Gower Street, London WC1E 6BT, UK.

出版信息

Philos Trans R Soc Lond B Biol Sci. 2020 Oct 12;375(1809):20190564. doi: 10.1098/rstb.2019.0564. Epub 2020 Aug 24.

DOI:10.1098/rstb.2019.0564
PMID:32829686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7482214/
Abstract

Tissue folding is a fundamental process that sculpts a simple flat epithelium into a complex three-dimensional organ structure. Whether it is the folding of the brain, or the looping of the gut, it has become clear that to generate an invagination or a fold of any form, mechanical asymmetries must exist in the epithelium. These mechanical asymmetries can be generated locally, involving just the invaginating cells and their immediate neighbours, or on a more global tissue-wide scale. Here, we review the different mechanical mechanisms that epithelia have adopted to generate folds, and how the use of precisely defined mathematical models has helped decipher which mechanisms are the key driving forces in different epithelia. This article is part of a discussion meeting issue 'Contemporary morphogenesis'.

摘要

组织折叠是一个基本过程,它将一个简单的平面上皮组织塑造成一个复杂的三维器官结构。无论是大脑的折叠,还是肠道的环曲,很明显,要产生任何形式的内陷或折叠,上皮组织中必须存在机械不对称性。这些机械不对称性可以局部产生,只涉及内陷细胞及其邻近的细胞,或者在更广泛的组织范围内产生。在这里,我们回顾了上皮组织采用的不同机械机制来产生褶皱,以及如何使用精确定义的数学模型来帮助揭示哪些机制是不同上皮组织中的关键驱动力。本文是“当代形态发生学”讨论会议的一部分。