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The Role of Tricellulin in Epithelial Jamming and Unjamming via Segmentation of Tricellular Junctions

Collective cellular behavior in confluent monolayers supports physiological and pathological processes of epithelial development, regeneration, and carcinogenesis. Here, the attainment of a mature and static tissue configuration or the local reactivation of cell motility involve a dynamic regulation...

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Autores principales: Lohmann, Sophie, Giampietro, Costanza, Pramotton, Francesca M., Al‐Nuaimi, Dunja, Poli, Alessandro, Maiuri, Paolo, Poulikakos, Dimos, Ferrari, Aldo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7404176/
https://www.ncbi.nlm.nih.gov/pubmed/32775171
http://dx.doi.org/10.1002/advs.202001213
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author Lohmann, Sophie
Giampietro, Costanza
Pramotton, Francesca M.
Al‐Nuaimi, Dunja
Poli, Alessandro
Maiuri, Paolo
Poulikakos, Dimos
Ferrari, Aldo
author_facet Lohmann, Sophie
Giampietro, Costanza
Pramotton, Francesca M.
Al‐Nuaimi, Dunja
Poli, Alessandro
Maiuri, Paolo
Poulikakos, Dimos
Ferrari, Aldo
author_sort Lohmann, Sophie
collection PubMed
description Collective cellular behavior in confluent monolayers supports physiological and pathological processes of epithelial development, regeneration, and carcinogenesis. Here, the attainment of a mature and static tissue configuration or the local reactivation of cell motility involve a dynamic regulation of the junctions established between neighboring cells. Tricellular junctions (tTJs), established at vertexes where three cells meet, are ideally located to control cellular shape and coordinate multicellular movements. However, their function in epithelial tissue dynamic remains poorly defined. To investigate the role of tTJs establishment and maturation in the jamming and unjamming transitions of epithelial monolayers, a semi‐automatic image‐processing pipeline is developed and validated enabling the unbiased and spatially resolved determination of the tTJ maturity state based on the localization of fluorescent reporters. The software resolves the variation of tTJ maturity accompanying collective transitions during tissue maturation, wound healing, and upon the adaptation to osmolarity changes. Altogether, this work establishes junctional maturity at tricellular contacts as a novel biological descriptor of collective responses in epithelial monolayers.
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spelling pubmed-74041762020-08-07 The Role of Tricellulin in Epithelial Jamming and Unjamming via Segmentation of Tricellular Junctions Lohmann, Sophie Giampietro, Costanza Pramotton, Francesca M. Al‐Nuaimi, Dunja Poli, Alessandro Maiuri, Paolo Poulikakos, Dimos Ferrari, Aldo Adv Sci (Weinh) Full Papers Collective cellular behavior in confluent monolayers supports physiological and pathological processes of epithelial development, regeneration, and carcinogenesis. Here, the attainment of a mature and static tissue configuration or the local reactivation of cell motility involve a dynamic regulation of the junctions established between neighboring cells. Tricellular junctions (tTJs), established at vertexes where three cells meet, are ideally located to control cellular shape and coordinate multicellular movements. However, their function in epithelial tissue dynamic remains poorly defined. To investigate the role of tTJs establishment and maturation in the jamming and unjamming transitions of epithelial monolayers, a semi‐automatic image‐processing pipeline is developed and validated enabling the unbiased and spatially resolved determination of the tTJ maturity state based on the localization of fluorescent reporters. The software resolves the variation of tTJ maturity accompanying collective transitions during tissue maturation, wound healing, and upon the adaptation to osmolarity changes. Altogether, this work establishes junctional maturity at tricellular contacts as a novel biological descriptor of collective responses in epithelial monolayers. John Wiley and Sons Inc. 2020-06-08 /pmc/articles/PMC7404176/ /pubmed/32775171 http://dx.doi.org/10.1002/advs.202001213 Text en © 2020 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Lohmann, Sophie
Giampietro, Costanza
Pramotton, Francesca M.
Al‐Nuaimi, Dunja
Poli, Alessandro
Maiuri, Paolo
Poulikakos, Dimos
Ferrari, Aldo
The Role of Tricellulin in Epithelial Jamming and Unjamming via Segmentation of Tricellular Junctions
title The Role of Tricellulin in Epithelial Jamming and Unjamming via Segmentation of Tricellular Junctions
title_full The Role of Tricellulin in Epithelial Jamming and Unjamming via Segmentation of Tricellular Junctions
title_fullStr The Role of Tricellulin in Epithelial Jamming and Unjamming via Segmentation of Tricellular Junctions
title_full_unstemmed The Role of Tricellulin in Epithelial Jamming and Unjamming via Segmentation of Tricellular Junctions
title_short The Role of Tricellulin in Epithelial Jamming and Unjamming via Segmentation of Tricellular Junctions
title_sort role of tricellulin in epithelial jamming and unjamming via segmentation of tricellular junctions
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7404176/
https://www.ncbi.nlm.nih.gov/pubmed/32775171
http://dx.doi.org/10.1002/advs.202001213
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