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  Integrin-Mediated Focal Anchorage Drives Epithelial Zippering during Mouse Neural Tube Closure

Mole, M. A., Galea, G. L., Rolo, A., Weberling, A., Nychyk, O., De Castro, S. C., et al. (2020). Integrin-Mediated Focal Anchorage Drives Epithelial Zippering during Mouse Neural Tube Closure. DEVELOPMENTAL CELL, 52(3), 321-334. doi:10.1016/j.devcel.2020.01.012.

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 Creators:
Mole, Matteo A.1, Author
Galea, Gabriel L.1, Author
Rolo, Ana1, Author
Weberling, Antonia1, Author
Nychyk, Oleksandr1, Author
De Castro, Sandra C.1, Author
Savery, Dawn1, Author
Fässler, Reinhard2, Author           
Ybot-Gonzalez, Patricia1, Author
Greene, Nicholas D. E.1, Author
Copp, Andrew J.1, Author
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1external, ou_persistent22              
2Fässler, Reinhard / Molecular Medicine, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565147              

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Free keywords: DORSAL CLOSURE; MORPHOGENESIS; FORCES; NEURULATION; ACTIVATION; APOPTOSIS; ADHESION; FUSION; CRE
 Abstract: Epithelial fusion is a key process of morphogenesis by which tissue connectivity is established between adjacent epithelial sheets. A striking and poorly understood feature of this process is "zippering," whereby a fusion point moves directionally along an organ rudiment. Here, we uncover the molecular mechanism underlying zippering during mouse spinal neural tube closure. Fusion is initiated via local activation of integrin beta 1 and focal anchorage of surface ectoderm cells to a shared point of fibronectin-rich basement membrane, where the neural folds first contact each other. Surface ectoderm cells undergo proximal junction shortening, establishing a transitory semi-rosette-like structure at the zippering point that promotes juxtaposition of cells across the midline enabling fusion propagation. Tissue-specific ablation of integrin beta 1 abolishes the semi-rosette formation, preventing zippering and causing spina bifida. We propose integrin-mediated anchorage as an evolutionarily conserved mechanism of general relevance for zippering closure of epithelial gaps whose disturbance can produce clinically important birth defects.

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Language(s): eng - English
 Dates: 2020
 Publication Status: Issued
 Pages: 20
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Degree: -

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Title: DEVELOPMENTAL CELL
Source Genre: Journal
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Publ. Info: 50 HAMPSHIRE ST, FLOOR 5, CAMBRIDGE, MA 02139 USA : CELL PRESS
Pages: - Volume / Issue: 52 (3) Sequence Number: - Start / End Page: 321 - 334 Identifier: ISSN: 1534-5807