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Fzd3 Expression Within Inner Ear Afferent Neurons Is Necessary for Central Pathfinding

During development the afferent neurons of the inner ear make precise wiring decisions in the hindbrain reflective of their topographic distribution in the periphery. This is critical for the formation of sensory maps capable of faithfully processing both auditory and vestibular input. Disorganized...

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Autores principales: Stoner, Zachary A., Ketchum, Elizabeth M., Sheltz-Kempf, Sydney, Blinkiewicz, Paige V., Elliott, Karen L., Duncan, Jeremy S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828977/
https://www.ncbi.nlm.nih.gov/pubmed/35153658
http://dx.doi.org/10.3389/fnins.2021.779871
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author Stoner, Zachary A.
Ketchum, Elizabeth M.
Sheltz-Kempf, Sydney
Blinkiewicz, Paige V.
Elliott, Karen L.
Duncan, Jeremy S.
author_facet Stoner, Zachary A.
Ketchum, Elizabeth M.
Sheltz-Kempf, Sydney
Blinkiewicz, Paige V.
Elliott, Karen L.
Duncan, Jeremy S.
author_sort Stoner, Zachary A.
collection PubMed
description During development the afferent neurons of the inner ear make precise wiring decisions in the hindbrain reflective of their topographic distribution in the periphery. This is critical for the formation of sensory maps capable of faithfully processing both auditory and vestibular input. Disorganized central projections of inner ear afferents in Fzd3 null mice indicate Wnt/PCP signaling is involved in this process and ear transplantation in Xenopus indicates that Fzd3 is necessary in the ear but not the hindbrain for proper afferent navigation. However, it remains unclear in which cell type of the inner ear Fzd3 expression is influencing the guidance of inner ear afferents to their proper synaptic targets in the hindbrain. We utilized Atoh1-cre and Neurod1-cre mouse lines to conditionally knockout Fzd3 within the mechanosensory hair cells of the organ of Corti and within the inner ear afferents, respectively. Following conditional deletion of Fzd3 within the hair cells, the central topographic distribution of inner ear afferents was maintained with no gross morphological defects. In contrast, conditional deletion of Fzd3 within inner ear afferents leads to central pathfinding defects of both cochlear and vestibular afferents. Here, we show that Fzd3 is acting in a cell autonomous manner within inner ear afferents to regulate central pathfinding within the hindbrain.
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spelling pubmed-88289772022-02-11 Fzd3 Expression Within Inner Ear Afferent Neurons Is Necessary for Central Pathfinding Stoner, Zachary A. Ketchum, Elizabeth M. Sheltz-Kempf, Sydney Blinkiewicz, Paige V. Elliott, Karen L. Duncan, Jeremy S. Front Neurosci Neuroscience During development the afferent neurons of the inner ear make precise wiring decisions in the hindbrain reflective of their topographic distribution in the periphery. This is critical for the formation of sensory maps capable of faithfully processing both auditory and vestibular input. Disorganized central projections of inner ear afferents in Fzd3 null mice indicate Wnt/PCP signaling is involved in this process and ear transplantation in Xenopus indicates that Fzd3 is necessary in the ear but not the hindbrain for proper afferent navigation. However, it remains unclear in which cell type of the inner ear Fzd3 expression is influencing the guidance of inner ear afferents to their proper synaptic targets in the hindbrain. We utilized Atoh1-cre and Neurod1-cre mouse lines to conditionally knockout Fzd3 within the mechanosensory hair cells of the organ of Corti and within the inner ear afferents, respectively. Following conditional deletion of Fzd3 within the hair cells, the central topographic distribution of inner ear afferents was maintained with no gross morphological defects. In contrast, conditional deletion of Fzd3 within inner ear afferents leads to central pathfinding defects of both cochlear and vestibular afferents. Here, we show that Fzd3 is acting in a cell autonomous manner within inner ear afferents to regulate central pathfinding within the hindbrain. Frontiers Media S.A. 2022-01-27 /pmc/articles/PMC8828977/ /pubmed/35153658 http://dx.doi.org/10.3389/fnins.2021.779871 Text en Copyright © 2022 Stoner, Ketchum, Sheltz-Kempf, Blinkiewicz, Elliott and Duncan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Stoner, Zachary A.
Ketchum, Elizabeth M.
Sheltz-Kempf, Sydney
Blinkiewicz, Paige V.
Elliott, Karen L.
Duncan, Jeremy S.
Fzd3 Expression Within Inner Ear Afferent Neurons Is Necessary for Central Pathfinding
title Fzd3 Expression Within Inner Ear Afferent Neurons Is Necessary for Central Pathfinding
title_full Fzd3 Expression Within Inner Ear Afferent Neurons Is Necessary for Central Pathfinding
title_fullStr Fzd3 Expression Within Inner Ear Afferent Neurons Is Necessary for Central Pathfinding
title_full_unstemmed Fzd3 Expression Within Inner Ear Afferent Neurons Is Necessary for Central Pathfinding
title_short Fzd3 Expression Within Inner Ear Afferent Neurons Is Necessary for Central Pathfinding
title_sort fzd3 expression within inner ear afferent neurons is necessary for central pathfinding
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828977/
https://www.ncbi.nlm.nih.gov/pubmed/35153658
http://dx.doi.org/10.3389/fnins.2021.779871
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