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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |