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本文引用的文献

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Regulation of neurogenesis by interkinetic nuclear migration through an apical-basal notch gradient.通过顶端-基底Notch梯度的动核迁移对神经发生的调控。
Cell. 2008 Sep 19;134(6):1055-65. doi: 10.1016/j.cell.2008.07.017.
2
In migrating cells, the Golgi complex and the position of the centrosome depend on geometrical constraints of the substratum.在迁移细胞中,高尔基体复合体和中心体的位置取决于基质的几何限制。
J Cell Sci. 2008 Jul 15;121(Pt 14):2406-14. doi: 10.1242/jcs.026849. Epub 2008 Jun 24.
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Epithelial-mesenchymal transition: at the crossroads of development and tumor metastasis.上皮-间质转化:处于发育与肿瘤转移的交叉点
Dev Cell. 2008 Jun;14(6):818-29. doi: 10.1016/j.devcel.2008.05.009.
4
A gene regulatory network orchestrates neural crest formation.一个基因调控网络协调神经嵴的形成。
Nat Rev Mol Cell Biol. 2008 Jul;9(7):557-68. doi: 10.1038/nrm2428. Epub 2008 Jun 4.
5
Transitions between epithelial and mesenchymal states in development and disease.发育和疾病过程中上皮状态与间充质状态之间的转变。
Semin Cell Dev Biol. 2008 Jun;19(3):294-308. doi: 10.1016/j.semcdb.2008.02.001. Epub 2008 Feb 9.
6
A critical role for Cadherin6B in regulating avian neural crest emigration.钙黏蛋白6B在调节鸟类神经嵴迁移中起关键作用。
Dev Biol. 2007 Dec 15;312(2):533-44. doi: 10.1016/j.ydbio.2007.09.056. Epub 2007 Oct 5.
7
Ets-1 confers cranial features on neural crest delamination.Ets-1赋予神经嵴脱层颅部特征。
PLoS One. 2007 Nov 7;2(11):e1142. doi: 10.1371/journal.pone.0001142.
8
Structure and mechanism of cadherins and catenins in cell-cell contacts.细胞间连接中钙黏蛋白和连环蛋白的结构与机制。
Annu Rev Cell Dev Biol. 2007;23:237-61. doi: 10.1146/annurev.cellbio.22.010305.104241.
9
Mitotic spindle orientation distinguishes stem cell and terminal modes of neuron production in the early spinal cord.有丝分裂纺锤体的方向区分了脊髓早期神经元产生的干细胞模式和终末模式。
Development. 2007 May;134(10):1943-54. doi: 10.1242/dev.002519.
10
Antagonistic roles of full-length N-cadherin and its soluble BMP cleavage product in neural crest delamination.全长N-钙黏蛋白及其可溶性骨形态发生蛋白裂解产物在神经嵴脱层中的拮抗作用。
Development. 2007 Feb;134(3):491-501. doi: 10.1242/dev.02742. Epub 2006 Dec 21.

4D视角下的神经嵴上皮-间充质转化:多种非必需细胞机制的“尾巴”

The neural crest epithelial-mesenchymal transition in 4D: a 'tail' of multiple non-obligatory cellular mechanisms.

作者信息

Ahlstrom Jon D, Erickson Carol A

机构信息

Molecular and Cellular Biology, University of California Davis, Davis, CA 95616, USA.

出版信息

Development. 2009 Jun;136(11):1801-12. doi: 10.1242/dev.034785.

DOI:10.1242/dev.034785
PMID:19429784
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2680107/
Abstract

An epithelial-mesenchymal transition (EMT) is the process whereby epithelial cells become mesenchymal cells, and is typified by the generation of neural crest cells from the neuroepithelium of the dorsal neural tube. To investigate the neural crest EMT, we performed live cell confocal time-lapse imaging to determine the sequence of cellular events and the role of cell division in the EMT. It was observed that in most EMTs, the apical cell tail is retracted cleanly from the lumen of the neuroepithelium, followed by movement of the cell body out of the neural tube. However, exceptions to this sequence include the rupture of the neural crest cell tail during retraction (junctional complexes not completely downregulated), or translocation of the cell body away from the apical surface while morphologically rounded up in M phase (no cell tail retraction event). We also noted that cell tail retraction can occur either before or after the redistribution of apical-basolateral epithelial polarity markers. Surprisingly, we discovered that when an EMT was preceded by a mitotic event, the plane of cytokinesis does not predict neural crest cell fate. Moreover, when daughter cells are separated from the adherens junctions by a parallel mitotic cleavage furrow, most re-establish contact with the apical surface. The diversity of cellular mechanisms by which neural crest cells can separate from the neural tube suggests that the EMT program is a complex network of non-linear mechanisms that can occur in multiple orders and combinations to allow neural crest cells to escape from the neuroepithelium.

摘要

上皮-间质转化(EMT)是上皮细胞转变为间质细胞的过程,其典型特征是从背侧神经管的神经上皮产生神经嵴细胞。为了研究神经嵴上皮-间质转化,我们进行了活细胞共聚焦延时成像,以确定细胞事件的顺序以及细胞分裂在该上皮-间质转化中的作用。据观察,在大多数上皮-间质转化过程中,顶端细胞尾从神经上皮管腔中干净地缩回,随后细胞体移出神经管。然而,该顺序的例外情况包括神经嵴细胞尾在缩回过程中破裂(连接复合体未完全下调),或者细胞体在M期形态变圆时从顶端表面移位离开(无细胞尾缩回事件)。我们还注意到,细胞尾缩回可发生在顶端-基底外侧上皮极性标记物重新分布之前或之后。令人惊讶的是,我们发现当上皮-间质转化之前发生有丝分裂事件时,胞质分裂平面并不能预测神经嵴细胞的命运。此外,当子细胞通过平行的有丝分裂分裂沟与黏附连接分离时,大多数子细胞会重新与顶端表面建立接触。神经嵴细胞从神经管分离的细胞机制的多样性表明,上皮-间质转化程序是一个复杂的非线性机制网络,这些机制可以以多种顺序和组合发生,以使神经嵴细胞从神经上皮中逸出。