Cargando…

Polycomb-Mediated Repression and Sonic Hedgehog Signaling Interact to Regulate Merkel Cell Specification during Skin Development

An increasing amount of evidence indicates that developmental programs are tightly regulated by the complex interplay between signaling pathways, as well as transcriptional and epigenetic processes. Here, we have uncovered coordination between transcriptional and morphogen cues to specify Merkel cel...

Descripción completa

Detalles Bibliográficos
Autores principales: Perdigoto, Carolina N., Dauber, Katherine L., Bar, Carmit, Tsai, Pai-Chi, Valdes, Victor J., Cohen, Idan, Santoriello, Francis J., Zhao, Dejian, Zheng, Deyou, Hsu, Ya-Chieh, Ezhkova, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4944976/
https://www.ncbi.nlm.nih.gov/pubmed/27414999
http://dx.doi.org/10.1371/journal.pgen.1006151
_version_ 1782442844234973184
author Perdigoto, Carolina N.
Dauber, Katherine L.
Bar, Carmit
Tsai, Pai-Chi
Valdes, Victor J.
Cohen, Idan
Santoriello, Francis J.
Zhao, Dejian
Zheng, Deyou
Hsu, Ya-Chieh
Ezhkova, Elena
author_facet Perdigoto, Carolina N.
Dauber, Katherine L.
Bar, Carmit
Tsai, Pai-Chi
Valdes, Victor J.
Cohen, Idan
Santoriello, Francis J.
Zhao, Dejian
Zheng, Deyou
Hsu, Ya-Chieh
Ezhkova, Elena
author_sort Perdigoto, Carolina N.
collection PubMed
description An increasing amount of evidence indicates that developmental programs are tightly regulated by the complex interplay between signaling pathways, as well as transcriptional and epigenetic processes. Here, we have uncovered coordination between transcriptional and morphogen cues to specify Merkel cells, poorly understood skin cells that mediate light touch sensations. In murine dorsal skin, Merkel cells are part of touch domes, which are skin structures consisting of specialized keratinocytes, Merkel cells, and afferent neurons, and are located exclusively around primary hair follicles. We show that the developing primary hair follicle functions as a niche required for Merkel cell specification. We find that intraepidermal Sonic hedgehog (Shh) signaling, initiated by the production of Shh ligand in the developing hair follicles, is required for Merkel cell specification. The importance of Shh for Merkel cell formation is further reinforced by the fact that Shh overexpression in embryonic epidermal progenitors leads to ectopic Merkel cells. Interestingly, Shh signaling is common to primary, secondary, and tertiary hair follicles, raising the possibility that there are restrictive mechanisms that regulate Merkel cell specification exclusively around primary hair follicles. Indeed, we find that loss of Polycomb repressive complex 2 (PRC2) in the epidermis results in the formation of ectopic Merkel cells that are associated with all hair types. We show that PRC2 loss expands the field of epidermal cells competent to differentiate into Merkel cells through the upregulation of key Merkel-differentiation genes, which are known PRC2 targets. Importantly, PRC2-mediated repression of the Merkel cell differentiation program requires inductive Shh signaling to form mature Merkel cells. Our study exemplifies how the interplay between epigenetic and morphogen cues regulates the complex patterning and formation of the mammalian skin structures.
format Online
Article
Text
id pubmed-4944976
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-49449762016-08-08 Polycomb-Mediated Repression and Sonic Hedgehog Signaling Interact to Regulate Merkel Cell Specification during Skin Development Perdigoto, Carolina N. Dauber, Katherine L. Bar, Carmit Tsai, Pai-Chi Valdes, Victor J. Cohen, Idan Santoriello, Francis J. Zhao, Dejian Zheng, Deyou Hsu, Ya-Chieh Ezhkova, Elena PLoS Genet Research Article An increasing amount of evidence indicates that developmental programs are tightly regulated by the complex interplay between signaling pathways, as well as transcriptional and epigenetic processes. Here, we have uncovered coordination between transcriptional and morphogen cues to specify Merkel cells, poorly understood skin cells that mediate light touch sensations. In murine dorsal skin, Merkel cells are part of touch domes, which are skin structures consisting of specialized keratinocytes, Merkel cells, and afferent neurons, and are located exclusively around primary hair follicles. We show that the developing primary hair follicle functions as a niche required for Merkel cell specification. We find that intraepidermal Sonic hedgehog (Shh) signaling, initiated by the production of Shh ligand in the developing hair follicles, is required for Merkel cell specification. The importance of Shh for Merkel cell formation is further reinforced by the fact that Shh overexpression in embryonic epidermal progenitors leads to ectopic Merkel cells. Interestingly, Shh signaling is common to primary, secondary, and tertiary hair follicles, raising the possibility that there are restrictive mechanisms that regulate Merkel cell specification exclusively around primary hair follicles. Indeed, we find that loss of Polycomb repressive complex 2 (PRC2) in the epidermis results in the formation of ectopic Merkel cells that are associated with all hair types. We show that PRC2 loss expands the field of epidermal cells competent to differentiate into Merkel cells through the upregulation of key Merkel-differentiation genes, which are known PRC2 targets. Importantly, PRC2-mediated repression of the Merkel cell differentiation program requires inductive Shh signaling to form mature Merkel cells. Our study exemplifies how the interplay between epigenetic and morphogen cues regulates the complex patterning and formation of the mammalian skin structures. Public Library of Science 2016-07-14 /pmc/articles/PMC4944976/ /pubmed/27414999 http://dx.doi.org/10.1371/journal.pgen.1006151 Text en © 2016 Perdigoto et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Perdigoto, Carolina N.
Dauber, Katherine L.
Bar, Carmit
Tsai, Pai-Chi
Valdes, Victor J.
Cohen, Idan
Santoriello, Francis J.
Zhao, Dejian
Zheng, Deyou
Hsu, Ya-Chieh
Ezhkova, Elena
Polycomb-Mediated Repression and Sonic Hedgehog Signaling Interact to Regulate Merkel Cell Specification during Skin Development
title Polycomb-Mediated Repression and Sonic Hedgehog Signaling Interact to Regulate Merkel Cell Specification during Skin Development
title_full Polycomb-Mediated Repression and Sonic Hedgehog Signaling Interact to Regulate Merkel Cell Specification during Skin Development
title_fullStr Polycomb-Mediated Repression and Sonic Hedgehog Signaling Interact to Regulate Merkel Cell Specification during Skin Development
title_full_unstemmed Polycomb-Mediated Repression and Sonic Hedgehog Signaling Interact to Regulate Merkel Cell Specification during Skin Development
title_short Polycomb-Mediated Repression and Sonic Hedgehog Signaling Interact to Regulate Merkel Cell Specification during Skin Development
title_sort polycomb-mediated repression and sonic hedgehog signaling interact to regulate merkel cell specification during skin development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4944976/
https://www.ncbi.nlm.nih.gov/pubmed/27414999
http://dx.doi.org/10.1371/journal.pgen.1006151
work_keys_str_mv AT perdigotocarolinan polycombmediatedrepressionandsonichedgehogsignalinginteracttoregulatemerkelcellspecificationduringskindevelopment
AT dauberkatherinel polycombmediatedrepressionandsonichedgehogsignalinginteracttoregulatemerkelcellspecificationduringskindevelopment
AT barcarmit polycombmediatedrepressionandsonichedgehogsignalinginteracttoregulatemerkelcellspecificationduringskindevelopment
AT tsaipaichi polycombmediatedrepressionandsonichedgehogsignalinginteracttoregulatemerkelcellspecificationduringskindevelopment
AT valdesvictorj polycombmediatedrepressionandsonichedgehogsignalinginteracttoregulatemerkelcellspecificationduringskindevelopment
AT cohenidan polycombmediatedrepressionandsonichedgehogsignalinginteracttoregulatemerkelcellspecificationduringskindevelopment
AT santoriellofrancisj polycombmediatedrepressionandsonichedgehogsignalinginteracttoregulatemerkelcellspecificationduringskindevelopment
AT zhaodejian polycombmediatedrepressionandsonichedgehogsignalinginteracttoregulatemerkelcellspecificationduringskindevelopment
AT zhengdeyou polycombmediatedrepressionandsonichedgehogsignalinginteracttoregulatemerkelcellspecificationduringskindevelopment
AT hsuyachieh polycombmediatedrepressionandsonichedgehogsignalinginteracttoregulatemerkelcellspecificationduringskindevelopment
AT ezhkovaelena polycombmediatedrepressionandsonichedgehogsignalinginteracttoregulatemerkelcellspecificationduringskindevelopment