Cargando…

Netrin-1 directs dendritic growth and connectivity of vertebrate central neurons in vivo

BACKGROUND: Netrins are a family of extracellular proteins that function as chemotropic guidance cues for migrating cells and axons during neural development. In the visual system, netrin-1 has been shown to play a key role in retinal ganglion cell (RGC) axon growth and branching at the target, wher...

Descripción completa

Detalles Bibliográficos
Autores principales: Nagel, Anastasia N., Marshak, Sonya, Manitt, Colleen, Santos, Rommel A., Piercy, Marc A., Mortero, Sarah D., Shirkey-Son, Nicole J., Cohen-Cory, Susana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481067/
https://www.ncbi.nlm.nih.gov/pubmed/26058786
http://dx.doi.org/10.1186/s13064-015-0041-y
_version_ 1782378233344294912
author Nagel, Anastasia N.
Marshak, Sonya
Manitt, Colleen
Santos, Rommel A.
Piercy, Marc A.
Mortero, Sarah D.
Shirkey-Son, Nicole J.
Cohen-Cory, Susana
author_facet Nagel, Anastasia N.
Marshak, Sonya
Manitt, Colleen
Santos, Rommel A.
Piercy, Marc A.
Mortero, Sarah D.
Shirkey-Son, Nicole J.
Cohen-Cory, Susana
author_sort Nagel, Anastasia N.
collection PubMed
description BACKGROUND: Netrins are a family of extracellular proteins that function as chemotropic guidance cues for migrating cells and axons during neural development. In the visual system, netrin-1 has been shown to play a key role in retinal ganglion cell (RGC) axon growth and branching at the target, where presynaptic RGC axons form partnerships with the dendrites of tectal neurons. However, the signals that guide the connections between RGC axons and their postsynaptic partners are yet unknown. Here, we explored dynamic cellular mechanisms by which netrin-1 influences visual circuit formation, particularly those that impact postsynaptic neuronal morphology and connectivity during retinotectal wiring. RESULTS: Time-lapse in vivo imaging of individual Xenopus laevis optic tectal neurons co-expressing tdTomato and PSD95-GFP revealed rapid remodeling and reorganization of dendritic arbors following acute manipulations in netrin-1 levels. Effects of altered netrin signaling on developing dendritic arbors of tectal neurons were distinct from its effects on presynaptic RGC axons. Within 4 h of treatment, tectal injection of recombinant netrin-1 or sequestration of endogenous netrin with an UNC-5 receptor ectodomain induced significant changes in the directionality and orientation of dendrite growth and in the maintenance of already established dendrites, demonstrating that relative levels of netrin are important for these functions. In contrast, altering DCC-mediated netrin signaling with function-blocking antibodies induced postsynaptic specialization remodeling and changed growth directionality of already established dendrites. Reducing netrin signaling also decreased avoidance behavior in a visually guided task, suggesting that netrin is essential for emergent visual system function. CONCLUSIONS: These in vivo findings together with the patterns of expression of netrin and its receptors reveal an important role for netrin in the early growth and guidance of vertebrate central neuron dendritic arbors. Collectively, our studies indicate that netrin shapes both pre- and postsynaptic arbor morphology directly and in multiple ways at stages critical for functional visual system development.
format Online
Article
Text
id pubmed-4481067
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-44810672015-06-27 Netrin-1 directs dendritic growth and connectivity of vertebrate central neurons in vivo Nagel, Anastasia N. Marshak, Sonya Manitt, Colleen Santos, Rommel A. Piercy, Marc A. Mortero, Sarah D. Shirkey-Son, Nicole J. Cohen-Cory, Susana Neural Dev Research Article BACKGROUND: Netrins are a family of extracellular proteins that function as chemotropic guidance cues for migrating cells and axons during neural development. In the visual system, netrin-1 has been shown to play a key role in retinal ganglion cell (RGC) axon growth and branching at the target, where presynaptic RGC axons form partnerships with the dendrites of tectal neurons. However, the signals that guide the connections between RGC axons and their postsynaptic partners are yet unknown. Here, we explored dynamic cellular mechanisms by which netrin-1 influences visual circuit formation, particularly those that impact postsynaptic neuronal morphology and connectivity during retinotectal wiring. RESULTS: Time-lapse in vivo imaging of individual Xenopus laevis optic tectal neurons co-expressing tdTomato and PSD95-GFP revealed rapid remodeling and reorganization of dendritic arbors following acute manipulations in netrin-1 levels. Effects of altered netrin signaling on developing dendritic arbors of tectal neurons were distinct from its effects on presynaptic RGC axons. Within 4 h of treatment, tectal injection of recombinant netrin-1 or sequestration of endogenous netrin with an UNC-5 receptor ectodomain induced significant changes in the directionality and orientation of dendrite growth and in the maintenance of already established dendrites, demonstrating that relative levels of netrin are important for these functions. In contrast, altering DCC-mediated netrin signaling with function-blocking antibodies induced postsynaptic specialization remodeling and changed growth directionality of already established dendrites. Reducing netrin signaling also decreased avoidance behavior in a visually guided task, suggesting that netrin is essential for emergent visual system function. CONCLUSIONS: These in vivo findings together with the patterns of expression of netrin and its receptors reveal an important role for netrin in the early growth and guidance of vertebrate central neuron dendritic arbors. Collectively, our studies indicate that netrin shapes both pre- and postsynaptic arbor morphology directly and in multiple ways at stages critical for functional visual system development. BioMed Central 2015-06-10 /pmc/articles/PMC4481067/ /pubmed/26058786 http://dx.doi.org/10.1186/s13064-015-0041-y Text en © Nagel et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Nagel, Anastasia N.
Marshak, Sonya
Manitt, Colleen
Santos, Rommel A.
Piercy, Marc A.
Mortero, Sarah D.
Shirkey-Son, Nicole J.
Cohen-Cory, Susana
Netrin-1 directs dendritic growth and connectivity of vertebrate central neurons in vivo
title Netrin-1 directs dendritic growth and connectivity of vertebrate central neurons in vivo
title_full Netrin-1 directs dendritic growth and connectivity of vertebrate central neurons in vivo
title_fullStr Netrin-1 directs dendritic growth and connectivity of vertebrate central neurons in vivo
title_full_unstemmed Netrin-1 directs dendritic growth and connectivity of vertebrate central neurons in vivo
title_short Netrin-1 directs dendritic growth and connectivity of vertebrate central neurons in vivo
title_sort netrin-1 directs dendritic growth and connectivity of vertebrate central neurons in vivo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481067/
https://www.ncbi.nlm.nih.gov/pubmed/26058786
http://dx.doi.org/10.1186/s13064-015-0041-y
work_keys_str_mv AT nagelanastasian netrin1directsdendriticgrowthandconnectivityofvertebratecentralneuronsinvivo
AT marshaksonya netrin1directsdendriticgrowthandconnectivityofvertebratecentralneuronsinvivo
AT manittcolleen netrin1directsdendriticgrowthandconnectivityofvertebratecentralneuronsinvivo
AT santosrommela netrin1directsdendriticgrowthandconnectivityofvertebratecentralneuronsinvivo
AT piercymarca netrin1directsdendriticgrowthandconnectivityofvertebratecentralneuronsinvivo
AT morterosarahd netrin1directsdendriticgrowthandconnectivityofvertebratecentralneuronsinvivo
AT shirkeysonnicolej netrin1directsdendriticgrowthandconnectivityofvertebratecentralneuronsinvivo
AT cohencorysusana netrin1directsdendriticgrowthandconnectivityofvertebratecentralneuronsinvivo