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

被引:77
|
作者
Ahlstrom, Jon D. [1 ]
Erickson, Carol A. [1 ]
机构
[1] Univ Calif Davis, Davis, CA 95616 USA
来源
DEVELOPMENT | 2009年 / 136卷 / 11期
关键词
EMT; Asymmetric division; Chicken; Live cell imaging; Neural crest; Neural tube; EPITHELIOMESENCHYMAL TRANSFORMATION; NUCLEAR-MOVEMENT; BETA-CATENIN; MIGRATION; CELLS; ONSET; DELAMINATION; LOCALIZATION; NEUROGENESIS; CENTROSOME;
D O I
10.1242/dev.034785
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:1801 / 1812
页数:12
相关论文
共 50 条
  • [41] Twist-1 is upregulated by NSD2 and contributes to tumour dissemination and an epithelial-mesenchymal transition-like gene expression signature in t (4;14)-positive multiple myeloma
    Cheong, Chee Man
    Mrozik, Krzysztof M.
    Hewett, Duncan R.
    Bell, Elyse
    Panagopoulos, Vasilios
    Noll, Jacqueline E.
    Licht, Jonathan D.
    Gronthos, Stan
    Zannettino, Andrew C. W.
    Vandyke, Kate
    CANCER LETTERS, 2020, 475 : 99 - 108
  • [42] Bone Marrow Mesenchymal Stem Cells (BMSCs)-Originated miR-1298 Impedes the Aggressiveness of Non-Small Cell Lung Cancer by Hindering the Chemokine Receptor 4 (CXCR4)-Induced Epithelial-Mesenchymal Transition (EMT) Process
    Nie, Guangjie
    Wei, Xiaoqun
    Ye, Jun
    JOURNAL OF BIOMATERIALS AND TISSUE ENGINEERING, 2022, 12 (06) : 1194 - 1201
  • [43] miR-363-3p inhibits migration, invasion, and epithelial-mesenchymal transition by targeting NEDD9 and SOX4 in non-small-cell lung cancer
    Chang, Jingxia
    Gao, Feng
    Chu, Heying
    Lou, Lili
    Wang, Huaqi
    Chen, Yibing
    JOURNAL OF CELLULAR PHYSIOLOGY, 2020, 235 (02) : 1808 - 1820
  • [44] Downregulation of miR-3127-5p promotes epithelial-mesenchymal transition via FZD4 regulation of Wnt/-catenin signaling in non-small-cell lung cancer
    Yang, Yang
    Sun, Yifeng
    Wu, Yun
    Tang, Dongfang
    Ding, Xi
    Xu, Wen
    Su, Bo
    Gao, Wen
    MOLECULAR CARCINOGENESIS, 2018, 57 (07) : 842 - 853
  • [45] Sprouty-4 Inhibits Transformed Cell Growth, Migration and Invasion, and Epithelial-Mesenchymal Transition, and Is Regulated by Wnt7A through PPARY in Non-Small Cell Lung Cancer
    Tennis, Meredith A.
    Van Scoyk, Michelle M.
    Freeman, Scott V.
    Vandervest, Katherine M.
    Nemenoff, Raphael A.
    Winn, Robert A.
    MOLECULAR CANCER RESEARCH, 2010, 8 (06) : 833 - 843
  • [46] Blocking OLFM4/HIF-1 axis alleviates hypoxia-induced invasion, epithelial-mesenchymal transition, and chemotherapy resistance in non-small-cell lung cancer
    Gao, Xian-Zheng
    Wang, Guan-Nan
    Zhao, Wu-Gan
    Han, Jing
    Diao, Chang-Ying
    Wang, Xiao-Hui
    Li, Sheng-Lei
    Li, Wen-Cai
    JOURNAL OF CELLULAR PHYSIOLOGY, 2019, 234 (09) : 15035 - 15043
  • [47] MYOCD and SMAD3/SMAD4 form a positive feedback loop and drive TGF-β-induced epithelial-mesenchymal transition in non-small cell lung cancer
    Tong, Xin
    Wang, Shengjie
    Lei, Zhe
    Li, Chang
    Zhang, Cuijuan
    Su, Zhiyue
    Liu, Xia
    Zhao, Jun
    Zhang, Hong-Tao
    ONCOGENE, 2020, 39 (14) : 2890 - 2904
  • [48] Alpha-Lipoic Acid-Me diate d Inhibition of LTB4 Synthesis Suppresses Epithelial-Mesenchymal Transition, Modulating Functional and Tumorigenic Capacities in Non-Small Cell Lung Cancer A549 Cells
    Torres, Maria Jose
    Rios, Juan Carlos
    Valle, Alexandra
    Indo, Sebastian
    Brockway, G. V. Kevin
    Lopez-Moncada, Fernanda
    Faundez, Mario
    Castellon, Enrique A.
    Contreras, Hector R.
    CURRENT THERAPEUTIC RESEARCH-CLINICAL AND EXPERIMENTAL, 2025, 102
  • [49] MiR-138 inhibits cell proliferation and reverses epithelial-mesenchymal transition in non-small cell lung cancer cells by targeting GIT1 and SEMA4C
    Li, Jiefang
    Wang, Qinrong
    Wen, Ruiling
    Liang, Jieman
    Zhong, Xiaoling
    Yang, Wei
    Su, Dongxiang
    Tang, Jun
    JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2015, 19 (12) : 2793 - 2805
  • [50] RGS6 suppresses TGF-β-induced epithelial-mesenchymal transition in non-small cell lung cancers via a novel mechanism dependent on its interaction with SMAD4
    Wang, Zhao
    Chen, Jun
    Wang, Shengjie
    Sun, Zelong
    Lei, Zhe
    Zhang, Hong-Tao
    Huang, Jie
    CELL DEATH & DISEASE, 2022, 13 (07)