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Abnormal Hair Development and Apparent Follicular Transformation to Mammary Gland in the Absence of Hedgehog Signaling
We show that removing the Shh signal tranducer Smoothened from skin epithelium secondarily results in excess Shh levels in the mesenchyme. Moreover, the phenotypes we observe reflect decreased epithelial Shh signaling, yet increased mesenchymal Shh signaling. For example, the latter contributes to e...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1885956/ https://www.ncbi.nlm.nih.gov/pubmed/17199044 http://dx.doi.org/10.1016/j.devcel.2006.12.006 |
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author | Gritli-Linde, Amel Hallberg, Kristina Harfe, Brian D. Reyahi, Azadeh Kannius-Janson, Marie Nilsson, Jeanette Cobourne, Martyn T. Sharpe, Paul T. McMahon, Andrew P. Linde, Anders |
author_facet | Gritli-Linde, Amel Hallberg, Kristina Harfe, Brian D. Reyahi, Azadeh Kannius-Janson, Marie Nilsson, Jeanette Cobourne, Martyn T. Sharpe, Paul T. McMahon, Andrew P. Linde, Anders |
author_sort | Gritli-Linde, Amel |
collection | PubMed |
description | We show that removing the Shh signal tranducer Smoothened from skin epithelium secondarily results in excess Shh levels in the mesenchyme. Moreover, the phenotypes we observe reflect decreased epithelial Shh signaling, yet increased mesenchymal Shh signaling. For example, the latter contributes to exuberant hair follicle (HF) induction, while the former depletes the resulting follicular stem cell niches. This disruption of the niche apparently also allows the remaining stem cells to initiate hair formation at inappropriate times. Thus, the temporal structure of the hair cycle may depend on the physical structure of the niche. Finally, we find that the ablation of epithelial Shh signaling results in unexpected transformations: the follicular outer root sheath takes on an epidermal character, and certain HFs disappear altogether, having adopted a strikingly mammary gland-like fate. Overall, our study uncovers a multifaceted function for Shh in sculpting and maintaining the integrity and identity of the developing HF. |
format | Text |
id | pubmed-1885956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-18859562007-06-11 Abnormal Hair Development and Apparent Follicular Transformation to Mammary Gland in the Absence of Hedgehog Signaling Gritli-Linde, Amel Hallberg, Kristina Harfe, Brian D. Reyahi, Azadeh Kannius-Janson, Marie Nilsson, Jeanette Cobourne, Martyn T. Sharpe, Paul T. McMahon, Andrew P. Linde, Anders Dev Cell Article We show that removing the Shh signal tranducer Smoothened from skin epithelium secondarily results in excess Shh levels in the mesenchyme. Moreover, the phenotypes we observe reflect decreased epithelial Shh signaling, yet increased mesenchymal Shh signaling. For example, the latter contributes to exuberant hair follicle (HF) induction, while the former depletes the resulting follicular stem cell niches. This disruption of the niche apparently also allows the remaining stem cells to initiate hair formation at inappropriate times. Thus, the temporal structure of the hair cycle may depend on the physical structure of the niche. Finally, we find that the ablation of epithelial Shh signaling results in unexpected transformations: the follicular outer root sheath takes on an epidermal character, and certain HFs disappear altogether, having adopted a strikingly mammary gland-like fate. Overall, our study uncovers a multifaceted function for Shh in sculpting and maintaining the integrity and identity of the developing HF. Cell Press 2007-01 /pmc/articles/PMC1885956/ /pubmed/17199044 http://dx.doi.org/10.1016/j.devcel.2006.12.006 Text en © 2007 ELL & Excerpta Medica. https://creativecommons.org/licenses/by/3.0/This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Gritli-Linde, Amel Hallberg, Kristina Harfe, Brian D. Reyahi, Azadeh Kannius-Janson, Marie Nilsson, Jeanette Cobourne, Martyn T. Sharpe, Paul T. McMahon, Andrew P. Linde, Anders Abnormal Hair Development and Apparent Follicular Transformation to Mammary Gland in the Absence of Hedgehog Signaling |
title | Abnormal Hair Development and Apparent Follicular Transformation to Mammary Gland in the Absence of Hedgehog Signaling |
title_full | Abnormal Hair Development and Apparent Follicular Transformation to Mammary Gland in the Absence of Hedgehog Signaling |
title_fullStr | Abnormal Hair Development and Apparent Follicular Transformation to Mammary Gland in the Absence of Hedgehog Signaling |
title_full_unstemmed | Abnormal Hair Development and Apparent Follicular Transformation to Mammary Gland in the Absence of Hedgehog Signaling |
title_short | Abnormal Hair Development and Apparent Follicular Transformation to Mammary Gland in the Absence of Hedgehog Signaling |
title_sort | abnormal hair development and apparent follicular transformation to mammary gland in the absence of hedgehog signaling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1885956/ https://www.ncbi.nlm.nih.gov/pubmed/17199044 http://dx.doi.org/10.1016/j.devcel.2006.12.006 |
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