Cargando…

Neuropilin-2/Semaphorin-3F-mediated repulsion promotes inner hair cell innervation by spiral ganglion neurons

Auditory function is dependent on the formation of specific innervation patterns between mechanosensory hair cells (HCs) and afferent spiral ganglion neurons (SGNs). In particular, type I SGNs must precisely connect with inner HCs (IHCs) while avoiding connections with nearby outer HCs (OHCs). The f...

Descripción completa

Detalles Bibliográficos
Autores principales: Coate, Thomas M, Spita, Nathalie A, Zhang, Kaidi D, Isgrig, Kevin T, Kelley, Matthew W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4566076/
https://www.ncbi.nlm.nih.gov/pubmed/26302206
http://dx.doi.org/10.7554/eLife.07830
_version_ 1782389668330864640
author Coate, Thomas M
Spita, Nathalie A
Zhang, Kaidi D
Isgrig, Kevin T
Kelley, Matthew W
author_facet Coate, Thomas M
Spita, Nathalie A
Zhang, Kaidi D
Isgrig, Kevin T
Kelley, Matthew W
author_sort Coate, Thomas M
collection PubMed
description Auditory function is dependent on the formation of specific innervation patterns between mechanosensory hair cells (HCs) and afferent spiral ganglion neurons (SGNs). In particular, type I SGNs must precisely connect with inner HCs (IHCs) while avoiding connections with nearby outer HCs (OHCs). The factors that mediate these patterning events are largely unknown. Using sparse-labeling and time-lapse imaging, we visualized for the first time the behaviors of developing SGNs including active retraction of processes from OHCs, suggesting that some type I SGNs contact OHCs before forming synapses with IHCs. In addition, we demonstrate that expression of Semaphorin-3F in the OHC region inhibits type I SGN process extension by activating Neuropilin-2 receptors expressed on SGNs. These results suggest a model in which cochlear innervation patterns by type I SGNs are determined, at least in part, through a Semaphorin-3F-mediated inhibitory signal that impedes processes from extending beyond the IHC region. DOI: http://dx.doi.org/10.7554/eLife.07830.001
format Online
Article
Text
id pubmed-4566076
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-45660762015-09-14 Neuropilin-2/Semaphorin-3F-mediated repulsion promotes inner hair cell innervation by spiral ganglion neurons Coate, Thomas M Spita, Nathalie A Zhang, Kaidi D Isgrig, Kevin T Kelley, Matthew W eLife Developmental Biology and Stem Cells Auditory function is dependent on the formation of specific innervation patterns between mechanosensory hair cells (HCs) and afferent spiral ganglion neurons (SGNs). In particular, type I SGNs must precisely connect with inner HCs (IHCs) while avoiding connections with nearby outer HCs (OHCs). The factors that mediate these patterning events are largely unknown. Using sparse-labeling and time-lapse imaging, we visualized for the first time the behaviors of developing SGNs including active retraction of processes from OHCs, suggesting that some type I SGNs contact OHCs before forming synapses with IHCs. In addition, we demonstrate that expression of Semaphorin-3F in the OHC region inhibits type I SGN process extension by activating Neuropilin-2 receptors expressed on SGNs. These results suggest a model in which cochlear innervation patterns by type I SGNs are determined, at least in part, through a Semaphorin-3F-mediated inhibitory signal that impedes processes from extending beyond the IHC region. DOI: http://dx.doi.org/10.7554/eLife.07830.001 eLife Sciences Publications, Ltd 2015-08-24 /pmc/articles/PMC4566076/ /pubmed/26302206 http://dx.doi.org/10.7554/eLife.07830 Text en http://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (http://creativecommons.org/publicdomain/zero/1.0/) .
spellingShingle Developmental Biology and Stem Cells
Coate, Thomas M
Spita, Nathalie A
Zhang, Kaidi D
Isgrig, Kevin T
Kelley, Matthew W
Neuropilin-2/Semaphorin-3F-mediated repulsion promotes inner hair cell innervation by spiral ganglion neurons
title Neuropilin-2/Semaphorin-3F-mediated repulsion promotes inner hair cell innervation by spiral ganglion neurons
title_full Neuropilin-2/Semaphorin-3F-mediated repulsion promotes inner hair cell innervation by spiral ganglion neurons
title_fullStr Neuropilin-2/Semaphorin-3F-mediated repulsion promotes inner hair cell innervation by spiral ganglion neurons
title_full_unstemmed Neuropilin-2/Semaphorin-3F-mediated repulsion promotes inner hair cell innervation by spiral ganglion neurons
title_short Neuropilin-2/Semaphorin-3F-mediated repulsion promotes inner hair cell innervation by spiral ganglion neurons
title_sort neuropilin-2/semaphorin-3f-mediated repulsion promotes inner hair cell innervation by spiral ganglion neurons
topic Developmental Biology and Stem Cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4566076/
https://www.ncbi.nlm.nih.gov/pubmed/26302206
http://dx.doi.org/10.7554/eLife.07830
work_keys_str_mv AT coatethomasm neuropilin2semaphorin3fmediatedrepulsionpromotesinnerhaircellinnervationbyspiralganglionneurons
AT spitanathaliea neuropilin2semaphorin3fmediatedrepulsionpromotesinnerhaircellinnervationbyspiralganglionneurons
AT zhangkaidid neuropilin2semaphorin3fmediatedrepulsionpromotesinnerhaircellinnervationbyspiralganglionneurons
AT isgrigkevint neuropilin2semaphorin3fmediatedrepulsionpromotesinnerhaircellinnervationbyspiralganglionneurons
AT kelleymattheww neuropilin2semaphorin3fmediatedrepulsionpromotesinnerhaircellinnervationbyspiralganglionneurons