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Tissue self-organization based on collective cell migration by contact activation of locomotion and chemotaxis
Despite their central role in multicellular organization, navigation rules that dictate cell rearrangement remain largely undefined. Contact between neighboring cells and diffusive attractant molecules are two of the major determinants of tissue-level patterning; however, in most cases, molecular an...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410881/ https://www.ncbi.nlm.nih.gov/pubmed/30782791 http://dx.doi.org/10.1073/pnas.1815063116 |
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author | Fujimori, Taihei Nakajima, Akihiko Shimada, Nao Sawai, Satoshi |
author_facet | Fujimori, Taihei Nakajima, Akihiko Shimada, Nao Sawai, Satoshi |
author_sort | Fujimori, Taihei |
collection | PubMed |
description | Despite their central role in multicellular organization, navigation rules that dictate cell rearrangement remain largely undefined. Contact between neighboring cells and diffusive attractant molecules are two of the major determinants of tissue-level patterning; however, in most cases, molecular and developmental complexity hinders one from decoding the exact governing rules of individual cell movement. A primordial example of tissue patterning by cell rearrangement is found in the social amoeba Dictyostelium discoideum where the organizing center or the “tip” self-organizes as a result of sorting of differentiating prestalk and prespore cells. By employing microfluidics and microsphere-based manipulation of navigational cues at the single-cell level, here we uncovered a previously overlooked mode of Dictyostelium cell migration that is strictly directed by cell–cell contact. The cell–cell contact signal is mediated by E-set Ig-like domain-containing heterophilic adhesion molecules TgrB1/TgrC1 that act in trans to induce plasma membrane recruitment of the SCAR complex and formation of dendritic actin networks, and the resulting cell protrusion competes with those induced by chemoattractant cAMP. Furthermore, we demonstrate that both prestalk and prespore cells can protrude toward the contact signal as well as to chemotax toward cAMP; however, when given both signals, prestalk cells orient toward the chemoattractant, whereas prespore cells choose the contact signal. These data suggest a model of cell sorting by competing juxtacrine and diffusive cues, each with potential to drive its own mode of collective cell migration. |
format | Online Article Text |
id | pubmed-6410881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-64108812019-03-13 Tissue self-organization based on collective cell migration by contact activation of locomotion and chemotaxis Fujimori, Taihei Nakajima, Akihiko Shimada, Nao Sawai, Satoshi Proc Natl Acad Sci U S A Biological Sciences Despite their central role in multicellular organization, navigation rules that dictate cell rearrangement remain largely undefined. Contact between neighboring cells and diffusive attractant molecules are two of the major determinants of tissue-level patterning; however, in most cases, molecular and developmental complexity hinders one from decoding the exact governing rules of individual cell movement. A primordial example of tissue patterning by cell rearrangement is found in the social amoeba Dictyostelium discoideum where the organizing center or the “tip” self-organizes as a result of sorting of differentiating prestalk and prespore cells. By employing microfluidics and microsphere-based manipulation of navigational cues at the single-cell level, here we uncovered a previously overlooked mode of Dictyostelium cell migration that is strictly directed by cell–cell contact. The cell–cell contact signal is mediated by E-set Ig-like domain-containing heterophilic adhesion molecules TgrB1/TgrC1 that act in trans to induce plasma membrane recruitment of the SCAR complex and formation of dendritic actin networks, and the resulting cell protrusion competes with those induced by chemoattractant cAMP. Furthermore, we demonstrate that both prestalk and prespore cells can protrude toward the contact signal as well as to chemotax toward cAMP; however, when given both signals, prestalk cells orient toward the chemoattractant, whereas prespore cells choose the contact signal. These data suggest a model of cell sorting by competing juxtacrine and diffusive cues, each with potential to drive its own mode of collective cell migration. National Academy of Sciences 2019-03-05 2019-02-19 /pmc/articles/PMC6410881/ /pubmed/30782791 http://dx.doi.org/10.1073/pnas.1815063116 Text en Copyright © 2019 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Fujimori, Taihei Nakajima, Akihiko Shimada, Nao Sawai, Satoshi Tissue self-organization based on collective cell migration by contact activation of locomotion and chemotaxis |
title | Tissue self-organization based on collective cell migration by contact activation of locomotion and chemotaxis |
title_full | Tissue self-organization based on collective cell migration by contact activation of locomotion and chemotaxis |
title_fullStr | Tissue self-organization based on collective cell migration by contact activation of locomotion and chemotaxis |
title_full_unstemmed | Tissue self-organization based on collective cell migration by contact activation of locomotion and chemotaxis |
title_short | Tissue self-organization based on collective cell migration by contact activation of locomotion and chemotaxis |
title_sort | tissue self-organization based on collective cell migration by contact activation of locomotion and chemotaxis |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410881/ https://www.ncbi.nlm.nih.gov/pubmed/30782791 http://dx.doi.org/10.1073/pnas.1815063116 |
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