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Phoenix Is Required for Mechanosensory Hair Cell Regeneration in the Zebrafish Lateral Line

In humans, the absence or irreversible loss of hair cells, the sensory mechanoreceptors in the cochlea, accounts for a large majority of acquired and congenital hearing disorders. In the auditory and vestibular neuroepithelia of the inner ear, hair cells are accompanied by another cell type called s...

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Autores principales: Behra, Martine, Bradsher, John, Sougrat, Rachid, Gallardo, Viviana, Allende, Miguel L., Burgess, Shawn M.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2662414/
https://www.ncbi.nlm.nih.gov/pubmed/19381250
http://dx.doi.org/10.1371/journal.pgen.1000455
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author Behra, Martine
Bradsher, John
Sougrat, Rachid
Gallardo, Viviana
Allende, Miguel L.
Burgess, Shawn M.
author_facet Behra, Martine
Bradsher, John
Sougrat, Rachid
Gallardo, Viviana
Allende, Miguel L.
Burgess, Shawn M.
author_sort Behra, Martine
collection PubMed
description In humans, the absence or irreversible loss of hair cells, the sensory mechanoreceptors in the cochlea, accounts for a large majority of acquired and congenital hearing disorders. In the auditory and vestibular neuroepithelia of the inner ear, hair cells are accompanied by another cell type called supporting cells. This second cell population has been described as having stem cell-like properties, allowing efficient hair cell replacement during embryonic and larval/fetal development of all vertebrates. However, mammals lose their regenerative capacity in most inner ear neuroepithelia in postnatal life. Remarkably, reptiles, birds, amphibians, and fish are different in that they can regenerate hair cells throughout their lifespan. The lateral line in amphibians and in fish is an additional sensory organ, which is used to detect water movements and is comprised of neuroepithelial patches, called neuromasts. These are similar in ultra-structure to the inner ear's neuroepithelia and they share the expression of various molecular markers. We examined the regeneration process in hair cells of the lateral line of zebrafish larvae carrying a retroviral integration in a previously uncharacterized gene, phoenix (pho). Phoenix mutant larvae develop normally and display a morphologically intact lateral line. However, after ablation of hair cells with copper or neomycin, their regeneration in pho mutants is severely impaired. We show that proliferation in the supporting cells is strongly decreased after damage to hair cells and correlates with the reduction of newly formed hair cells in the regenerating phoenix mutant neuromasts. The retroviral integration linked to the phenotype is in a novel gene with no known homologs showing high expression in neuromast supporting cells. Whereas its role during early development of the lateral line remains to be addressed, in later larval stages phoenix defines a new class of proteins implicated in hair cell regeneration.
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spelling pubmed-26624142009-04-17 Phoenix Is Required for Mechanosensory Hair Cell Regeneration in the Zebrafish Lateral Line Behra, Martine Bradsher, John Sougrat, Rachid Gallardo, Viviana Allende, Miguel L. Burgess, Shawn M. PLoS Genet Research Article In humans, the absence or irreversible loss of hair cells, the sensory mechanoreceptors in the cochlea, accounts for a large majority of acquired and congenital hearing disorders. In the auditory and vestibular neuroepithelia of the inner ear, hair cells are accompanied by another cell type called supporting cells. This second cell population has been described as having stem cell-like properties, allowing efficient hair cell replacement during embryonic and larval/fetal development of all vertebrates. However, mammals lose their regenerative capacity in most inner ear neuroepithelia in postnatal life. Remarkably, reptiles, birds, amphibians, and fish are different in that they can regenerate hair cells throughout their lifespan. The lateral line in amphibians and in fish is an additional sensory organ, which is used to detect water movements and is comprised of neuroepithelial patches, called neuromasts. These are similar in ultra-structure to the inner ear's neuroepithelia and they share the expression of various molecular markers. We examined the regeneration process in hair cells of the lateral line of zebrafish larvae carrying a retroviral integration in a previously uncharacterized gene, phoenix (pho). Phoenix mutant larvae develop normally and display a morphologically intact lateral line. However, after ablation of hair cells with copper or neomycin, their regeneration in pho mutants is severely impaired. We show that proliferation in the supporting cells is strongly decreased after damage to hair cells and correlates with the reduction of newly formed hair cells in the regenerating phoenix mutant neuromasts. The retroviral integration linked to the phenotype is in a novel gene with no known homologs showing high expression in neuromast supporting cells. Whereas its role during early development of the lateral line remains to be addressed, in later larval stages phoenix defines a new class of proteins implicated in hair cell regeneration. Public Library of Science 2009-04-17 /pmc/articles/PMC2662414/ /pubmed/19381250 http://dx.doi.org/10.1371/journal.pgen.1000455 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Behra, Martine
Bradsher, John
Sougrat, Rachid
Gallardo, Viviana
Allende, Miguel L.
Burgess, Shawn M.
Phoenix Is Required for Mechanosensory Hair Cell Regeneration in the Zebrafish Lateral Line
title Phoenix Is Required for Mechanosensory Hair Cell Regeneration in the Zebrafish Lateral Line
title_full Phoenix Is Required for Mechanosensory Hair Cell Regeneration in the Zebrafish Lateral Line
title_fullStr Phoenix Is Required for Mechanosensory Hair Cell Regeneration in the Zebrafish Lateral Line
title_full_unstemmed Phoenix Is Required for Mechanosensory Hair Cell Regeneration in the Zebrafish Lateral Line
title_short Phoenix Is Required for Mechanosensory Hair Cell Regeneration in the Zebrafish Lateral Line
title_sort phoenix is required for mechanosensory hair cell regeneration in the zebrafish lateral line
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2662414/
https://www.ncbi.nlm.nih.gov/pubmed/19381250
http://dx.doi.org/10.1371/journal.pgen.1000455
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