Dynamic fibronectin assembly and remodeling by leader neural crest cells prevents jamming in collective cell migration

<p>Collective cell migration plays an essential role in vertebrate development, yet the extent to which dynamically changing microenvironments influence this phenomenon remains unclear. Observations of the distribution of the extracellular matrix (ECM) component fibronectin during the migratio...

Full description

Bibliographic Details
Main Authors: Martinson, W, McLennan, R, Teddy, J, McKinney, M, Davidson, L, Baker, R, Byrne, H, Kulesa, P, Maini, P
Format: Journal article
Language:English
Published: eLife Sciences Publications 2023
_version_ 1797110325839921152
author Martinson, W
McLennan, R
Teddy, J
McKinney, M
Davidson, L
Baker, R
Byrne, H
Kulesa, P
Maini, P
author_facet Martinson, W
McLennan, R
Teddy, J
McKinney, M
Davidson, L
Baker, R
Byrne, H
Kulesa, P
Maini, P
author_sort Martinson, W
collection OXFORD
description <p>Collective cell migration plays an essential role in vertebrate development, yet the extent to which dynamically changing microenvironments influence this phenomenon remains unclear. Observations of the distribution of the extracellular matrix (ECM) component fibronectin during the migration of loosely connected neural crest cells (NCCs) lead us to hypothesize that NCC remodeling of an initially punctate ECM creates a scaffold for trailing cells, enabling them to form robust and coherent stream patterns. We evaluate this idea in a theoretical setting by developing an individual-based computational model that incorporates reciprocal interactions between NCCs and their ECM. ECM remodeling, haptotaxis, contact guidance, and cell-cell repulsion are sufficient for cells to establish streams in silico, however, additional mechanisms, such as chemotaxis, are required to consistently guide cells along the correct target corridor. Further model investigations imply that contact guidance and differential cell-cell repulsion between leader and follower cells are key contributors to robust collective cell migration by preventing stream breakage. Global sensitivity analysis and simulated gain- and loss-of-function experiments suggest that long-distance migration without jamming is most likely to occur when leading cells specialize in creating ECM fibers, and trailing cells specialize in responding to environmental cues by upregulating mechanisms such as contact guidance.</p>
first_indexed 2024-03-07T07:53:24Z
format Journal article
id oxford-uuid:b84e6651-8539-4616-bb51-57377d740511
institution University of Oxford
language English
last_indexed 2024-03-07T07:53:24Z
publishDate 2023
publisher eLife Sciences Publications
record_format dspace
spelling oxford-uuid:b84e6651-8539-4616-bb51-57377d7405112023-07-27T11:32:03ZDynamic fibronectin assembly and remodeling by leader neural crest cells prevents jamming in collective cell migrationJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:b84e6651-8539-4616-bb51-57377d740511EnglishSymplectic ElementseLife Sciences Publications2023Martinson, WMcLennan, RTeddy, JMcKinney, MDavidson, LBaker, RByrne, HKulesa, PMaini, P<p>Collective cell migration plays an essential role in vertebrate development, yet the extent to which dynamically changing microenvironments influence this phenomenon remains unclear. Observations of the distribution of the extracellular matrix (ECM) component fibronectin during the migration of loosely connected neural crest cells (NCCs) lead us to hypothesize that NCC remodeling of an initially punctate ECM creates a scaffold for trailing cells, enabling them to form robust and coherent stream patterns. We evaluate this idea in a theoretical setting by developing an individual-based computational model that incorporates reciprocal interactions between NCCs and their ECM. ECM remodeling, haptotaxis, contact guidance, and cell-cell repulsion are sufficient for cells to establish streams in silico, however, additional mechanisms, such as chemotaxis, are required to consistently guide cells along the correct target corridor. Further model investigations imply that contact guidance and differential cell-cell repulsion between leader and follower cells are key contributors to robust collective cell migration by preventing stream breakage. Global sensitivity analysis and simulated gain- and loss-of-function experiments suggest that long-distance migration without jamming is most likely to occur when leading cells specialize in creating ECM fibers, and trailing cells specialize in responding to environmental cues by upregulating mechanisms such as contact guidance.</p>
spellingShingle Martinson, W
McLennan, R
Teddy, J
McKinney, M
Davidson, L
Baker, R
Byrne, H
Kulesa, P
Maini, P
Dynamic fibronectin assembly and remodeling by leader neural crest cells prevents jamming in collective cell migration
title Dynamic fibronectin assembly and remodeling by leader neural crest cells prevents jamming in collective cell migration
title_full Dynamic fibronectin assembly and remodeling by leader neural crest cells prevents jamming in collective cell migration
title_fullStr Dynamic fibronectin assembly and remodeling by leader neural crest cells prevents jamming in collective cell migration
title_full_unstemmed Dynamic fibronectin assembly and remodeling by leader neural crest cells prevents jamming in collective cell migration
title_short Dynamic fibronectin assembly and remodeling by leader neural crest cells prevents jamming in collective cell migration
title_sort dynamic fibronectin assembly and remodeling by leader neural crest cells prevents jamming in collective cell migration
work_keys_str_mv AT martinsonw dynamicfibronectinassemblyandremodelingbyleaderneuralcrestcellspreventsjammingincollectivecellmigration
AT mclennanr dynamicfibronectinassemblyandremodelingbyleaderneuralcrestcellspreventsjammingincollectivecellmigration
AT teddyj dynamicfibronectinassemblyandremodelingbyleaderneuralcrestcellspreventsjammingincollectivecellmigration
AT mckinneym dynamicfibronectinassemblyandremodelingbyleaderneuralcrestcellspreventsjammingincollectivecellmigration
AT davidsonl dynamicfibronectinassemblyandremodelingbyleaderneuralcrestcellspreventsjammingincollectivecellmigration
AT bakerr dynamicfibronectinassemblyandremodelingbyleaderneuralcrestcellspreventsjammingincollectivecellmigration
AT byrneh dynamicfibronectinassemblyandremodelingbyleaderneuralcrestcellspreventsjammingincollectivecellmigration
AT kulesap dynamicfibronectinassemblyandremodelingbyleaderneuralcrestcellspreventsjammingincollectivecellmigration
AT mainip dynamicfibronectinassemblyandremodelingbyleaderneuralcrestcellspreventsjammingincollectivecellmigration