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Dendritic atoh1a+ cells serve as transient intermediates during zebrafish Merkel cell development and regeneration

Sensory cells often adopt specific morphologies that aid in the detection of external stimuli. Merkel cells encode gentle touch stimuli in vertebrate skin and adopt a reproducible shape characterized by spiky, actin-rich microvilli that emanate from the cell surface. The mechanism by which Merkel ce...

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Autores principales: Craig, Evan W., Black, Erik C., Goo, Camille E.A., Swearer, Avery Angell, Yee, Nathaniel G., Rasmussen, Jeffrey P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515958/
https://www.ncbi.nlm.nih.gov/pubmed/37745341
http://dx.doi.org/10.1101/2023.09.14.557830
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author Craig, Evan W.
Black, Erik C.
Goo, Camille E.A.
Swearer, Avery Angell
Yee, Nathaniel G.
Rasmussen, Jeffrey P.
author_facet Craig, Evan W.
Black, Erik C.
Goo, Camille E.A.
Swearer, Avery Angell
Yee, Nathaniel G.
Rasmussen, Jeffrey P.
author_sort Craig, Evan W.
collection PubMed
description Sensory cells often adopt specific morphologies that aid in the detection of external stimuli. Merkel cells encode gentle touch stimuli in vertebrate skin and adopt a reproducible shape characterized by spiky, actin-rich microvilli that emanate from the cell surface. The mechanism by which Merkel cells acquire this stereotyped morphology from basal keratinocyte progenitors is unknown. Here, we establish that dendritic Merkel cells (dMCs) express atonal homolog 1a (atoh1a), extend dynamic filopodial processes, and arise in transient waves during zebrafish skin development and regeneration. We find that dMCs share molecular similarities with both basal keratinocytes and Merkel cells, yet display mesenchymal-like behaviors, including local cell motility and proliferation within the epidermis. Furthermore, dMCs can directly adopt the mature, microvilliated Merkel cell morphology through substantial remodeling of the actin cytoskeleton. Loss of Ectodysplasin A signaling alters the morphology of dMCs and Merkel cells within specific skin regions. Our results show that dMCs represent an intermediate state in the Merkel cell maturation program and identify Ectodysplasin A signaling as a key regulator of Merkel cell morphology.
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spelling pubmed-105159582023-09-23 Dendritic atoh1a+ cells serve as transient intermediates during zebrafish Merkel cell development and regeneration Craig, Evan W. Black, Erik C. Goo, Camille E.A. Swearer, Avery Angell Yee, Nathaniel G. Rasmussen, Jeffrey P. bioRxiv Article Sensory cells often adopt specific morphologies that aid in the detection of external stimuli. Merkel cells encode gentle touch stimuli in vertebrate skin and adopt a reproducible shape characterized by spiky, actin-rich microvilli that emanate from the cell surface. The mechanism by which Merkel cells acquire this stereotyped morphology from basal keratinocyte progenitors is unknown. Here, we establish that dendritic Merkel cells (dMCs) express atonal homolog 1a (atoh1a), extend dynamic filopodial processes, and arise in transient waves during zebrafish skin development and regeneration. We find that dMCs share molecular similarities with both basal keratinocytes and Merkel cells, yet display mesenchymal-like behaviors, including local cell motility and proliferation within the epidermis. Furthermore, dMCs can directly adopt the mature, microvilliated Merkel cell morphology through substantial remodeling of the actin cytoskeleton. Loss of Ectodysplasin A signaling alters the morphology of dMCs and Merkel cells within specific skin regions. Our results show that dMCs represent an intermediate state in the Merkel cell maturation program and identify Ectodysplasin A signaling as a key regulator of Merkel cell morphology. Cold Spring Harbor Laboratory 2023-09-25 /pmc/articles/PMC10515958/ /pubmed/37745341 http://dx.doi.org/10.1101/2023.09.14.557830 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Craig, Evan W.
Black, Erik C.
Goo, Camille E.A.
Swearer, Avery Angell
Yee, Nathaniel G.
Rasmussen, Jeffrey P.
Dendritic atoh1a+ cells serve as transient intermediates during zebrafish Merkel cell development and regeneration
title Dendritic atoh1a+ cells serve as transient intermediates during zebrafish Merkel cell development and regeneration
title_full Dendritic atoh1a+ cells serve as transient intermediates during zebrafish Merkel cell development and regeneration
title_fullStr Dendritic atoh1a+ cells serve as transient intermediates during zebrafish Merkel cell development and regeneration
title_full_unstemmed Dendritic atoh1a+ cells serve as transient intermediates during zebrafish Merkel cell development and regeneration
title_short Dendritic atoh1a+ cells serve as transient intermediates during zebrafish Merkel cell development and regeneration
title_sort dendritic atoh1a+ cells serve as transient intermediates during zebrafish merkel cell development and regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515958/
https://www.ncbi.nlm.nih.gov/pubmed/37745341
http://dx.doi.org/10.1101/2023.09.14.557830
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