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Migration and fate of vestibular melanocytes during the development of the human inner ear

Melanocytes are present in various parts of the inner ear, including the stria vascularis in the cochlea and the dark cell areas in the vestibular organs, where they contribute to endolymph homeostasis. Developmental studies describing the distribution of vestibular melanocytes are scarce, especiall...

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Autores principales: van Beelen, Edward S. A., van der Valk, Wouter H., de Groot, John C. M. J., Hensen, Erik F., Locher, Heiko, van Benthem, Peter Paul G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894185/
https://www.ncbi.nlm.nih.gov/pubmed/33075185
http://dx.doi.org/10.1002/dneu.22786
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author van Beelen, Edward S. A.
van der Valk, Wouter H.
de Groot, John C. M. J.
Hensen, Erik F.
Locher, Heiko
van Benthem, Peter Paul G.
author_facet van Beelen, Edward S. A.
van der Valk, Wouter H.
de Groot, John C. M. J.
Hensen, Erik F.
Locher, Heiko
van Benthem, Peter Paul G.
author_sort van Beelen, Edward S. A.
collection PubMed
description Melanocytes are present in various parts of the inner ear, including the stria vascularis in the cochlea and the dark cell areas in the vestibular organs, where they contribute to endolymph homeostasis. Developmental studies describing the distribution of vestibular melanocytes are scarce, especially in humans. In this study, we investigated the distribution and maturation of the vestibular melanocytes in relation to the developing dark cell epithelium in inner ear specimens from week 5 to week 14 of development and in surgical specimens of the adult ampulla. Vestibular melanocytes were located around the utricle and the ampullae of the semicircular canals before week 7 and were first seen underneath the transitional zones and dark cell areas between week 8 and week 10. At week 10, melanocytes made intimate contact with epithelial cells, interrupting the local basement membrane with their dendritic processes. At week 11, most melanocytes were positioned under the dark cell epithelia. No melanocytes were seen around or in the saccule during all investigated developmental stages. The dark cell areas gradually matured and showed an adult immunohistochemical profile of the characteristic ion transporter protein Na(+)/K(+)‐ATPase α1 by week 14. Furthermore, we investigated the expression of the migration‐related proteins ECAD, PCAD, KIT, and KITLG in melanocytes and dark cell epithelium. This is the first study to describe the spatiotemporal distribution of vestibular melanocytes during the human development and thereby contributes to understanding normal vestibular function and pathophysiological mechanisms underlying vestibular disorders.
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spelling pubmed-78941852021-03-02 Migration and fate of vestibular melanocytes during the development of the human inner ear van Beelen, Edward S. A. van der Valk, Wouter H. de Groot, John C. M. J. Hensen, Erik F. Locher, Heiko van Benthem, Peter Paul G. Dev Neurobiol Research Articles Melanocytes are present in various parts of the inner ear, including the stria vascularis in the cochlea and the dark cell areas in the vestibular organs, where they contribute to endolymph homeostasis. Developmental studies describing the distribution of vestibular melanocytes are scarce, especially in humans. In this study, we investigated the distribution and maturation of the vestibular melanocytes in relation to the developing dark cell epithelium in inner ear specimens from week 5 to week 14 of development and in surgical specimens of the adult ampulla. Vestibular melanocytes were located around the utricle and the ampullae of the semicircular canals before week 7 and were first seen underneath the transitional zones and dark cell areas between week 8 and week 10. At week 10, melanocytes made intimate contact with epithelial cells, interrupting the local basement membrane with their dendritic processes. At week 11, most melanocytes were positioned under the dark cell epithelia. No melanocytes were seen around or in the saccule during all investigated developmental stages. The dark cell areas gradually matured and showed an adult immunohistochemical profile of the characteristic ion transporter protein Na(+)/K(+)‐ATPase α1 by week 14. Furthermore, we investigated the expression of the migration‐related proteins ECAD, PCAD, KIT, and KITLG in melanocytes and dark cell epithelium. This is the first study to describe the spatiotemporal distribution of vestibular melanocytes during the human development and thereby contributes to understanding normal vestibular function and pathophysiological mechanisms underlying vestibular disorders. John Wiley and Sons Inc. 2020-11-02 2020 /pmc/articles/PMC7894185/ /pubmed/33075185 http://dx.doi.org/10.1002/dneu.22786 Text en © The Authors. Developmental Neurobiology published by 2020 Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
van Beelen, Edward S. A.
van der Valk, Wouter H.
de Groot, John C. M. J.
Hensen, Erik F.
Locher, Heiko
van Benthem, Peter Paul G.
Migration and fate of vestibular melanocytes during the development of the human inner ear
title Migration and fate of vestibular melanocytes during the development of the human inner ear
title_full Migration and fate of vestibular melanocytes during the development of the human inner ear
title_fullStr Migration and fate of vestibular melanocytes during the development of the human inner ear
title_full_unstemmed Migration and fate of vestibular melanocytes during the development of the human inner ear
title_short Migration and fate of vestibular melanocytes during the development of the human inner ear
title_sort migration and fate of vestibular melanocytes during the development of the human inner ear
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894185/
https://www.ncbi.nlm.nih.gov/pubmed/33075185
http://dx.doi.org/10.1002/dneu.22786
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