Cargando…

Gradients of glucose metabolism regulate morphogen signalling required for specifying tonotopic organisation in the chicken cochlea

In vertebrates with elongated auditory organs, mechanosensory hair cells (HCs) are organised such that complex sounds are broken down into their component frequencies along a proximal-to-distal long (tonotopic) axis. Acquisition of unique morphologies at the appropriate position along the chick coch...

Descripción completa

Detalles Bibliográficos
Autores principales: O'Sullivan, James DB, Blacker, Thomas S, Scott, Claire, Chang, Weise, Ahmed, Mohi, Yianni, Val, Mann, Zoe F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425173/
https://www.ncbi.nlm.nih.gov/pubmed/37539863
http://dx.doi.org/10.7554/eLife.86233
_version_ 1785089779332808704
author O'Sullivan, James DB
Blacker, Thomas S
Scott, Claire
Chang, Weise
Ahmed, Mohi
Yianni, Val
Mann, Zoe F
author_facet O'Sullivan, James DB
Blacker, Thomas S
Scott, Claire
Chang, Weise
Ahmed, Mohi
Yianni, Val
Mann, Zoe F
author_sort O'Sullivan, James DB
collection PubMed
description In vertebrates with elongated auditory organs, mechanosensory hair cells (HCs) are organised such that complex sounds are broken down into their component frequencies along a proximal-to-distal long (tonotopic) axis. Acquisition of unique morphologies at the appropriate position along the chick cochlea, the basilar papilla, requires that nascent HCs determine their tonotopic positions during development. The complex signalling within the auditory organ between a developing HC and its local niche along the cochlea is poorly understood. Using a combination of live imaging and NAD(P)H fluorescence lifetime imaging microscopy, we reveal that there is a gradient in the cellular balance between glycolysis and the pentose phosphate pathway in developing HCs along the tonotopic axis. Perturbing this balance by inhibiting different branches of cytosolic glucose catabolism disrupts developmental morphogen signalling and abolishes the normal tonotopic gradient in HC morphology. These findings highlight a causal link between graded morphogen signalling and metabolic reprogramming in specifying the tonotopic identity of developing HCs.
format Online
Article
Text
id pubmed-10425173
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-104251732023-08-15 Gradients of glucose metabolism regulate morphogen signalling required for specifying tonotopic organisation in the chicken cochlea O'Sullivan, James DB Blacker, Thomas S Scott, Claire Chang, Weise Ahmed, Mohi Yianni, Val Mann, Zoe F eLife Cell Biology In vertebrates with elongated auditory organs, mechanosensory hair cells (HCs) are organised such that complex sounds are broken down into their component frequencies along a proximal-to-distal long (tonotopic) axis. Acquisition of unique morphologies at the appropriate position along the chick cochlea, the basilar papilla, requires that nascent HCs determine their tonotopic positions during development. The complex signalling within the auditory organ between a developing HC and its local niche along the cochlea is poorly understood. Using a combination of live imaging and NAD(P)H fluorescence lifetime imaging microscopy, we reveal that there is a gradient in the cellular balance between glycolysis and the pentose phosphate pathway in developing HCs along the tonotopic axis. Perturbing this balance by inhibiting different branches of cytosolic glucose catabolism disrupts developmental morphogen signalling and abolishes the normal tonotopic gradient in HC morphology. These findings highlight a causal link between graded morphogen signalling and metabolic reprogramming in specifying the tonotopic identity of developing HCs. eLife Sciences Publications, Ltd 2023-08-04 /pmc/articles/PMC10425173/ /pubmed/37539863 http://dx.doi.org/10.7554/eLife.86233 Text en https://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 (https://creativecommons.org/publicdomain/zero/1.0/) .
spellingShingle Cell Biology
O'Sullivan, James DB
Blacker, Thomas S
Scott, Claire
Chang, Weise
Ahmed, Mohi
Yianni, Val
Mann, Zoe F
Gradients of glucose metabolism regulate morphogen signalling required for specifying tonotopic organisation in the chicken cochlea
title Gradients of glucose metabolism regulate morphogen signalling required for specifying tonotopic organisation in the chicken cochlea
title_full Gradients of glucose metabolism regulate morphogen signalling required for specifying tonotopic organisation in the chicken cochlea
title_fullStr Gradients of glucose metabolism regulate morphogen signalling required for specifying tonotopic organisation in the chicken cochlea
title_full_unstemmed Gradients of glucose metabolism regulate morphogen signalling required for specifying tonotopic organisation in the chicken cochlea
title_short Gradients of glucose metabolism regulate morphogen signalling required for specifying tonotopic organisation in the chicken cochlea
title_sort gradients of glucose metabolism regulate morphogen signalling required for specifying tonotopic organisation in the chicken cochlea
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425173/
https://www.ncbi.nlm.nih.gov/pubmed/37539863
http://dx.doi.org/10.7554/eLife.86233
work_keys_str_mv AT osullivanjamesdb gradientsofglucosemetabolismregulatemorphogensignallingrequiredforspecifyingtonotopicorganisationinthechickencochlea
AT blackerthomass gradientsofglucosemetabolismregulatemorphogensignallingrequiredforspecifyingtonotopicorganisationinthechickencochlea
AT scottclaire gradientsofglucosemetabolismregulatemorphogensignallingrequiredforspecifyingtonotopicorganisationinthechickencochlea
AT changweise gradientsofglucosemetabolismregulatemorphogensignallingrequiredforspecifyingtonotopicorganisationinthechickencochlea
AT ahmedmohi gradientsofglucosemetabolismregulatemorphogensignallingrequiredforspecifyingtonotopicorganisationinthechickencochlea
AT yiannival gradientsofglucosemetabolismregulatemorphogensignallingrequiredforspecifyingtonotopicorganisationinthechickencochlea
AT mannzoef gradientsofglucosemetabolismregulatemorphogensignallingrequiredforspecifyingtonotopicorganisationinthechickencochlea