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Dermal appendage-dependent patterning of zebrafish atoh1a+ Merkel cells

Touch system function requires precise interactions between specialized skin cells and somatosensory axons, as exemplified by the vertebrate mechanosensory Merkel cell-neurite complex. Development and patterning of Merkel cells and associated neurites during skin organogenesis remain poorly understo...

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Autores principales: Brown, Tanya L, Horton, Emma C, Craig, Evan W, Goo, Camille EA, Black, Erik C, Hewitt, Madeleine N, Yee, Nathaniel G, Fan, Everett T, Raible, David W, Rasmussen, Jeffrey P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9901935/
https://www.ncbi.nlm.nih.gov/pubmed/36648063
http://dx.doi.org/10.7554/eLife.85800
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author Brown, Tanya L
Horton, Emma C
Craig, Evan W
Goo, Camille EA
Black, Erik C
Hewitt, Madeleine N
Yee, Nathaniel G
Fan, Everett T
Raible, David W
Rasmussen, Jeffrey P
author_facet Brown, Tanya L
Horton, Emma C
Craig, Evan W
Goo, Camille EA
Black, Erik C
Hewitt, Madeleine N
Yee, Nathaniel G
Fan, Everett T
Raible, David W
Rasmussen, Jeffrey P
author_sort Brown, Tanya L
collection PubMed
description Touch system function requires precise interactions between specialized skin cells and somatosensory axons, as exemplified by the vertebrate mechanosensory Merkel cell-neurite complex. Development and patterning of Merkel cells and associated neurites during skin organogenesis remain poorly understood, partly due to the in utero development of mammalian embryos. Here, we discover Merkel cells in the zebrafish epidermis and identify Atonal homolog 1a (Atoh1a) as a marker of zebrafish Merkel cells. We show that zebrafish Merkel cells derive from basal keratinocytes, express neurosecretory and mechanosensory machinery, extend actin-rich microvilli, and complex with somatosensory axons, all hallmarks of mammalian Merkel cells. Merkel cells populate all major adult skin compartments, with region-specific densities and distribution patterns. In vivo photoconversion reveals that Merkel cells undergo steady loss and replenishment during skin homeostasis. Merkel cells develop concomitant with dermal appendages along the trunk and loss of Ectodysplasin signaling, which prevents dermal appendage formation, reduces Merkel cell density by affecting cell differentiation. By contrast, altering dermal appendage morphology changes the distribution, but not density, of Merkel cells. Overall, our studies provide insights into touch system maturation during skin organogenesis and establish zebrafish as an experimentally accessible in vivo model for the study of Merkel cell biology.
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spelling pubmed-99019352023-02-07 Dermal appendage-dependent patterning of zebrafish atoh1a+ Merkel cells Brown, Tanya L Horton, Emma C Craig, Evan W Goo, Camille EA Black, Erik C Hewitt, Madeleine N Yee, Nathaniel G Fan, Everett T Raible, David W Rasmussen, Jeffrey P eLife Developmental Biology Touch system function requires precise interactions between specialized skin cells and somatosensory axons, as exemplified by the vertebrate mechanosensory Merkel cell-neurite complex. Development and patterning of Merkel cells and associated neurites during skin organogenesis remain poorly understood, partly due to the in utero development of mammalian embryos. Here, we discover Merkel cells in the zebrafish epidermis and identify Atonal homolog 1a (Atoh1a) as a marker of zebrafish Merkel cells. We show that zebrafish Merkel cells derive from basal keratinocytes, express neurosecretory and mechanosensory machinery, extend actin-rich microvilli, and complex with somatosensory axons, all hallmarks of mammalian Merkel cells. Merkel cells populate all major adult skin compartments, with region-specific densities and distribution patterns. In vivo photoconversion reveals that Merkel cells undergo steady loss and replenishment during skin homeostasis. Merkel cells develop concomitant with dermal appendages along the trunk and loss of Ectodysplasin signaling, which prevents dermal appendage formation, reduces Merkel cell density by affecting cell differentiation. By contrast, altering dermal appendage morphology changes the distribution, but not density, of Merkel cells. Overall, our studies provide insights into touch system maturation during skin organogenesis and establish zebrafish as an experimentally accessible in vivo model for the study of Merkel cell biology. eLife Sciences Publications, Ltd 2023-01-17 /pmc/articles/PMC9901935/ /pubmed/36648063 http://dx.doi.org/10.7554/eLife.85800 Text en © 2023, Brown, Horton et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Brown, Tanya L
Horton, Emma C
Craig, Evan W
Goo, Camille EA
Black, Erik C
Hewitt, Madeleine N
Yee, Nathaniel G
Fan, Everett T
Raible, David W
Rasmussen, Jeffrey P
Dermal appendage-dependent patterning of zebrafish atoh1a+ Merkel cells
title Dermal appendage-dependent patterning of zebrafish atoh1a+ Merkel cells
title_full Dermal appendage-dependent patterning of zebrafish atoh1a+ Merkel cells
title_fullStr Dermal appendage-dependent patterning of zebrafish atoh1a+ Merkel cells
title_full_unstemmed Dermal appendage-dependent patterning of zebrafish atoh1a+ Merkel cells
title_short Dermal appendage-dependent patterning of zebrafish atoh1a+ Merkel cells
title_sort dermal appendage-dependent patterning of zebrafish atoh1a+ merkel cells
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9901935/
https://www.ncbi.nlm.nih.gov/pubmed/36648063
http://dx.doi.org/10.7554/eLife.85800
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