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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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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. |
format | Online Article Text |
id | pubmed-7404176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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