Cadherin-2 Is Required Cell Autonomously for Collective Migration of Facial Branchiomotor Neurons.

Collective migration depends on cell-cell interactions between neighbors that contribute to their overall directionality, yet the mechanisms that control the coordinated migration of neurons remains to be elucidated. During hindbrain development, facial branchiomotor neurons (FBMNs) undergo a stereo...

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Main Authors: Jane K Rebman, Kathryn E Kirchoff, Gregory S Walsh
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5055392?pdf=render
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spelling doaj-449590f41ccf49f8ae6241f857cd209f2020-11-25T02:36:42ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-011110e016443310.1371/journal.pone.0164433Cadherin-2 Is Required Cell Autonomously for Collective Migration of Facial Branchiomotor Neurons.Jane K RebmanKathryn E KirchoffGregory S WalshCollective migration depends on cell-cell interactions between neighbors that contribute to their overall directionality, yet the mechanisms that control the coordinated migration of neurons remains to be elucidated. During hindbrain development, facial branchiomotor neurons (FBMNs) undergo a stereotypic tangential caudal migration from their place of birth in rhombomere (r)4 to their final location in r6/7. FBMNs engage in collective cell migration that depends on neuron-to-neuron interactions to facilitate caudal directionality. Here, we demonstrate that Cadherin-2-mediated neuron-to-neuron adhesion is necessary for directional and collective migration of FBMNs. We generated stable transgenic zebrafish expressing dominant-negative Cadherin-2 (Cdh2ΔEC) driven by the islet1 promoter. Cell-autonomous inactivation of Cadherin-2 function led to non-directional migration of FBMNs and a defect in caudal tangential migration. Additionally, mosaic analysis revealed that Cdh2ΔEC-expressing FBMNs are not influenced to migrate caudally by neighboring wild-type FBMNs due to a defect in collective cell migration. Taken together, our data suggest that Cadherin-2 plays an essential cell-autonomous role in mediating the collective migration of FBMNs.http://europepmc.org/articles/PMC5055392?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jane K Rebman
Kathryn E Kirchoff
Gregory S Walsh
spellingShingle Jane K Rebman
Kathryn E Kirchoff
Gregory S Walsh
Cadherin-2 Is Required Cell Autonomously for Collective Migration of Facial Branchiomotor Neurons.
PLoS ONE
author_facet Jane K Rebman
Kathryn E Kirchoff
Gregory S Walsh
author_sort Jane K Rebman
title Cadherin-2 Is Required Cell Autonomously for Collective Migration of Facial Branchiomotor Neurons.
title_short Cadherin-2 Is Required Cell Autonomously for Collective Migration of Facial Branchiomotor Neurons.
title_full Cadherin-2 Is Required Cell Autonomously for Collective Migration of Facial Branchiomotor Neurons.
title_fullStr Cadherin-2 Is Required Cell Autonomously for Collective Migration of Facial Branchiomotor Neurons.
title_full_unstemmed Cadherin-2 Is Required Cell Autonomously for Collective Migration of Facial Branchiomotor Neurons.
title_sort cadherin-2 is required cell autonomously for collective migration of facial branchiomotor neurons.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2016-01-01
description Collective migration depends on cell-cell interactions between neighbors that contribute to their overall directionality, yet the mechanisms that control the coordinated migration of neurons remains to be elucidated. During hindbrain development, facial branchiomotor neurons (FBMNs) undergo a stereotypic tangential caudal migration from their place of birth in rhombomere (r)4 to their final location in r6/7. FBMNs engage in collective cell migration that depends on neuron-to-neuron interactions to facilitate caudal directionality. Here, we demonstrate that Cadherin-2-mediated neuron-to-neuron adhesion is necessary for directional and collective migration of FBMNs. We generated stable transgenic zebrafish expressing dominant-negative Cadherin-2 (Cdh2ΔEC) driven by the islet1 promoter. Cell-autonomous inactivation of Cadherin-2 function led to non-directional migration of FBMNs and a defect in caudal tangential migration. Additionally, mosaic analysis revealed that Cdh2ΔEC-expressing FBMNs are not influenced to migrate caudally by neighboring wild-type FBMNs due to a defect in collective cell migration. Taken together, our data suggest that Cadherin-2 plays an essential cell-autonomous role in mediating the collective migration of FBMNs.
url http://europepmc.org/articles/PMC5055392?pdf=render
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AT gregoryswalsh cadherin2isrequiredcellautonomouslyforcollectivemigrationoffacialbranchiomotorneurons
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