Neural crest streaming as an emergent property of tissue interactions during morphogenesis.

A fundamental question in embryo morphogenesis is how a complex pattern is established in seemingly uniform tissues. During vertebrate development, neural crest cells differentiate as a continuous mass of tissue along the neural tube and subsequently split into spatially distinct migratory streams t...

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Main Authors: András Szabó, Eric Theveneau, Melissa Turan, Roberto Mayor
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-04-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1007002
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spelling doaj-62e4b62785db43f2ac571812d2d00a232021-04-21T15:11:31ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582019-04-01154e100700210.1371/journal.pcbi.1007002Neural crest streaming as an emergent property of tissue interactions during morphogenesis.András SzabóEric TheveneauMelissa TuranRoberto MayorA fundamental question in embryo morphogenesis is how a complex pattern is established in seemingly uniform tissues. During vertebrate development, neural crest cells differentiate as a continuous mass of tissue along the neural tube and subsequently split into spatially distinct migratory streams to invade the rest of the embryo. How these streams are established is not well understood. Inhibitory signals surrounding the migratory streams led to the idea that position and size of streams are determined by a pre-pattern of such signals. While clear evidence for a pre-pattern in the cranial region is still lacking, all computational models of neural crest migration published so far have assumed a pre-pattern of negative signals that channel the neural crest into streams. Here we test the hypothesis that instead of following a pre-existing pattern, the cranial neural crest creates their own migratory pathway by interacting with the surrounding tissue. By combining theoretical modeling with experimentation, we show that streams emerge from the interaction of the hindbrain neural crest and the neighboring epibranchial placodal tissues, without the need for a pre-existing guidance cue. Our model suggests that the initial collective neural crest invasion is based on short-range repulsion and asymmetric attraction between neighboring tissues. The model provides a coherent explanation for the formation of cranial neural crest streams in concert with previously reported findings and our new in vivo observations. Our results point to a general mechanism of inducing collective invasion patterns.https://doi.org/10.1371/journal.pcbi.1007002
collection DOAJ
language English
format Article
sources DOAJ
author András Szabó
Eric Theveneau
Melissa Turan
Roberto Mayor
spellingShingle András Szabó
Eric Theveneau
Melissa Turan
Roberto Mayor
Neural crest streaming as an emergent property of tissue interactions during morphogenesis.
PLoS Computational Biology
author_facet András Szabó
Eric Theveneau
Melissa Turan
Roberto Mayor
author_sort András Szabó
title Neural crest streaming as an emergent property of tissue interactions during morphogenesis.
title_short Neural crest streaming as an emergent property of tissue interactions during morphogenesis.
title_full Neural crest streaming as an emergent property of tissue interactions during morphogenesis.
title_fullStr Neural crest streaming as an emergent property of tissue interactions during morphogenesis.
title_full_unstemmed Neural crest streaming as an emergent property of tissue interactions during morphogenesis.
title_sort neural crest streaming as an emergent property of tissue interactions during morphogenesis.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2019-04-01
description A fundamental question in embryo morphogenesis is how a complex pattern is established in seemingly uniform tissues. During vertebrate development, neural crest cells differentiate as a continuous mass of tissue along the neural tube and subsequently split into spatially distinct migratory streams to invade the rest of the embryo. How these streams are established is not well understood. Inhibitory signals surrounding the migratory streams led to the idea that position and size of streams are determined by a pre-pattern of such signals. While clear evidence for a pre-pattern in the cranial region is still lacking, all computational models of neural crest migration published so far have assumed a pre-pattern of negative signals that channel the neural crest into streams. Here we test the hypothesis that instead of following a pre-existing pattern, the cranial neural crest creates their own migratory pathway by interacting with the surrounding tissue. By combining theoretical modeling with experimentation, we show that streams emerge from the interaction of the hindbrain neural crest and the neighboring epibranchial placodal tissues, without the need for a pre-existing guidance cue. Our model suggests that the initial collective neural crest invasion is based on short-range repulsion and asymmetric attraction between neighboring tissues. The model provides a coherent explanation for the formation of cranial neural crest streams in concert with previously reported findings and our new in vivo observations. Our results point to a general mechanism of inducing collective invasion patterns.
url https://doi.org/10.1371/journal.pcbi.1007002
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