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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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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 |
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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 |
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