Characterizing the Cellular Nature of the Physical Interactions Necessary for Collective Neuron Migration

Neuronal migration is an essential process in the development of the nervous system. Neurons are born in one location and migrate sizable distances to their final location. In many other developmental processes, cells migrate as collectives, where the migration of one cell influences the migration o...

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Main Author: Vareed, Rebecca
Format: Others
Published: VCU Scholars Compass 2019
Subjects:
Online Access:https://scholarscompass.vcu.edu/etd/5895
https://scholarscompass.vcu.edu/cgi/viewcontent.cgi?article=7013&context=etd
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spelling ndltd-vcu.edu-oai-scholarscompass.vcu.edu-etd-70132019-10-20T22:09:26Z Characterizing the Cellular Nature of the Physical Interactions Necessary for Collective Neuron Migration Vareed, Rebecca Neuronal migration is an essential process in the development of the nervous system. Neurons are born in one location and migrate sizable distances to their final location. In many other developmental processes, cells migrate as collectives, where the migration of one cell influences the migration of another cell; this process has yet to be shown in the developing central nervous system. Using the conserved tangential migration of facial branchiomotor neurons (FBMNs), I aim to determine the nature of the collective migration in the developing nervous system. Here, two models of FBMN collective migration are tested: the “Pioneer” model, where following FBMNs migrate intimately on the axon of the first neuron to migrate and the “Contact inhibition of locomotion (CIL)” model, where transient cell-cell contacts are the driving influence of the proper caudal migration of FBMNs. Using fixed tissue imaging, it was found that early born FBMNs do not contact the axon. In contrast, they are more likely to make soma-soma contact and display morphology typical of CIL. FBMNs that do contact the axon do not display an elongated morphology that is predicted of a cell using the leader axon as a substrate for migration. Further, wild-type FBMNs are able to rescue PCP-deficient FBMNs. Therefore, blastula-stage transplantation of PCP-deficient neurons into wild-type hosts allows us to live image the method of collective migration. CIL events were observed between PCP-deficient neurons and wild-type neurons, indicating that PCP is not required for CIL. In addition, PCP-deficient neurons making sustained contact with wildtype axons were not rescued, arguing against the Pioneer model. Taken together, these observations are more consistent with the “CIL” model of FBMN collective migration in which transient soma-soma interactions are required for the coordinated movement of neurons as they migrate in the developing nervous system. 2019-01-01T08:00:00Z text application/pdf https://scholarscompass.vcu.edu/etd/5895 https://scholarscompass.vcu.edu/cgi/viewcontent.cgi?article=7013&context=etd © Rebecca D. Vareed Theses and Dissertations VCU Scholars Compass Facial branchiomotor neurons development collective migration neuroscience Developmental Neuroscience
collection NDLTD
format Others
sources NDLTD
topic Facial branchiomotor neurons
development
collective migration
neuroscience
Developmental Neuroscience
spellingShingle Facial branchiomotor neurons
development
collective migration
neuroscience
Developmental Neuroscience
Vareed, Rebecca
Characterizing the Cellular Nature of the Physical Interactions Necessary for Collective Neuron Migration
description Neuronal migration is an essential process in the development of the nervous system. Neurons are born in one location and migrate sizable distances to their final location. In many other developmental processes, cells migrate as collectives, where the migration of one cell influences the migration of another cell; this process has yet to be shown in the developing central nervous system. Using the conserved tangential migration of facial branchiomotor neurons (FBMNs), I aim to determine the nature of the collective migration in the developing nervous system. Here, two models of FBMN collective migration are tested: the “Pioneer” model, where following FBMNs migrate intimately on the axon of the first neuron to migrate and the “Contact inhibition of locomotion (CIL)” model, where transient cell-cell contacts are the driving influence of the proper caudal migration of FBMNs. Using fixed tissue imaging, it was found that early born FBMNs do not contact the axon. In contrast, they are more likely to make soma-soma contact and display morphology typical of CIL. FBMNs that do contact the axon do not display an elongated morphology that is predicted of a cell using the leader axon as a substrate for migration. Further, wild-type FBMNs are able to rescue PCP-deficient FBMNs. Therefore, blastula-stage transplantation of PCP-deficient neurons into wild-type hosts allows us to live image the method of collective migration. CIL events were observed between PCP-deficient neurons and wild-type neurons, indicating that PCP is not required for CIL. In addition, PCP-deficient neurons making sustained contact with wildtype axons were not rescued, arguing against the Pioneer model. Taken together, these observations are more consistent with the “CIL” model of FBMN collective migration in which transient soma-soma interactions are required for the coordinated movement of neurons as they migrate in the developing nervous system.
author Vareed, Rebecca
author_facet Vareed, Rebecca
author_sort Vareed, Rebecca
title Characterizing the Cellular Nature of the Physical Interactions Necessary for Collective Neuron Migration
title_short Characterizing the Cellular Nature of the Physical Interactions Necessary for Collective Neuron Migration
title_full Characterizing the Cellular Nature of the Physical Interactions Necessary for Collective Neuron Migration
title_fullStr Characterizing the Cellular Nature of the Physical Interactions Necessary for Collective Neuron Migration
title_full_unstemmed Characterizing the Cellular Nature of the Physical Interactions Necessary for Collective Neuron Migration
title_sort characterizing the cellular nature of the physical interactions necessary for collective neuron migration
publisher VCU Scholars Compass
publishDate 2019
url https://scholarscompass.vcu.edu/etd/5895
https://scholarscompass.vcu.edu/cgi/viewcontent.cgi?article=7013&context=etd
work_keys_str_mv AT vareedrebecca characterizingthecellularnatureofthephysicalinteractionsnecessaryforcollectiveneuronmigration
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