Scientific article
English

Adherens Junction Length during Tissue Contraction Is Controlled by the Mechanosensitive Activity of Actomyosin and Junctional Recycling

Published inDevelopmental cell, vol. 47, no. 4, p. 453-463.e3
Publication date2018-11
Abstract

During epithelial contraction, cells generate forces to constrict their surface and, concurrently, fine-tune the length of their adherens junctions to ensure force transmission. While many studies have focused on understanding force generation, little is known on how junctional length is controlled. Here, we show that, during amnioserosa contraction in Drosophila dorsal closure, adherens junctions reduce their length in coordination with the shrinkage of apical cell area, maintaining a nearly constant junctional straightness. We reveal that junctional straightness and integrity depend on the endocytic machinery and on the mechanosensitive activity of the actomyosin cytoskeleton. On one hand, upon junctional stretch and decrease in E-cadherin density, actomyosin relocalizes from the medial area to the junctions, thus maintaining junctional integrity. On the other hand, when junctions have excess material and ruffles, junction removal is enhanced, and high junctional straightness and tension are restored. These two mechanisms control junctional length and integrity during morphogenesis.

Keywords
  • Drosophila dorsal closure
  • E-cadherin
  • Actomyosin cytoskeleton
  • Adherens junction
  • Biophysical modeling
  • Endocytosis
  • Epithelial contraction
  • Morphogenesis
Affiliation entities Not a UNIGE publication
Funding
  • Wellcome Trust - Theoretical Physics of Biology Laboratory [FC001317]
  • the Spanish Ministry of Economy, Industry and Competitiveness (MEIC) [BFU2010-16546]
  • The Francis Crick Institute [10317]
  • Cancer Research UK [21144]
  • Generalitat de Catalunya
Citation (ISO format)
SUMI, Angughali et al. Adherens Junction Length during Tissue Contraction Is Controlled by the Mechanosensitive Activity of Actomyosin and Junctional Recycling. In: Developmental cell, 2018, vol. 47, n° 4, p. 453–463.e3. doi: 10.1016/j.devcel.2018.10.025
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Article (Published version)
accessLevelRestricted
Identifiers
Journal ISSN1534-5807
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