Microtubule-dependent balanced cell contraction and luminal-matrix modification accelerate epithelial tube fusion
Kagayaki Kato,
Bo Dong,
Housei Wada,
Miho Tanaka-Matakatsu,
Yoshimasa Yagi and
Shigeo Hayashi ()
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Kagayaki Kato: Laboratory for Morphogenetic Signaling, RIKEN Center for Developmental Biology
Bo Dong: Laboratory for Morphogenetic Signaling, RIKEN Center for Developmental Biology
Housei Wada: Laboratory for Morphogenetic Signaling, RIKEN Center for Developmental Biology
Miho Tanaka-Matakatsu: Feinberg School of Medicine, Northwestern University
Yoshimasa Yagi: Graduate School of Science, Nagoya University
Shigeo Hayashi: Laboratory for Morphogenetic Signaling, RIKEN Center for Developmental Biology
Nature Communications, 2016, vol. 7, issue 1, 1-11
Abstract:
Abstract Connection of tubules into larger networks is the key process for the development of circulatory systems. In Drosophila development, tip cells of the tracheal system lead the migration of each branch and connect tubules by adhering to each other and simultaneously changing into a torus-shape. We show that as adhesion sites form between fusion cells, myosin and microtubules form polarized bundles that connect the new adhesion site to the cells’ microtubule-organizing centres, and that E-cadherin and retrograde recycling endosomes are preferentially deposited at the new adhesion site. We demonstrate that microtubules help balancing tip cell contraction, which is driven by myosin, and is required for adhesion and tube fusion. We also show that retrograde recycling and directed secretion of a specific matrix protein into the fusion-cell interface promote fusion. We propose that microtubule bundles connecting these cell–cell interfaces coordinate cell contractility and apical secretion to facilitate tube fusion.
Date: 2016
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms11141
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DOI: 10.1038/ncomms11141
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