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Epidermal-Derived Hedgehog Signaling Drives Mesenchymal Proliferation during Digit Tip Regeneration
Hand injuries often result in significant functional impairments and are rarely completely restored. The spontaneous regeneration of injured appendages, which occurs in salamanders and newts, for example, has been reported in human fingertips after distal amputation, but this type of regeneration is...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8467649/ https://www.ncbi.nlm.nih.gov/pubmed/34575372 http://dx.doi.org/10.3390/jcm10184261 |
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author | Maan, Zeshaan N. Rinkevich, Yuval Barrera, Janos Chen, Kellen Henn, Dominic Foster, Deshka Bonham, Clark Andrew Padmanabhan, Jagannath Sivaraj, Dharshan Duscher, Dominik Hu, Michael Yan, Kelley Januszyk, Michael Longaker, Michael T. Weissman, Irving L. Gurtner, Geoffrey C. |
author_facet | Maan, Zeshaan N. Rinkevich, Yuval Barrera, Janos Chen, Kellen Henn, Dominic Foster, Deshka Bonham, Clark Andrew Padmanabhan, Jagannath Sivaraj, Dharshan Duscher, Dominik Hu, Michael Yan, Kelley Januszyk, Michael Longaker, Michael T. Weissman, Irving L. Gurtner, Geoffrey C. |
author_sort | Maan, Zeshaan N. |
collection | PubMed |
description | Hand injuries often result in significant functional impairments and are rarely completely restored. The spontaneous regeneration of injured appendages, which occurs in salamanders and newts, for example, has been reported in human fingertips after distal amputation, but this type of regeneration is rare in mammals and is incompletely understood. Here, we study fingertip regeneration by amputating murine digit tips, either distally to initiate regeneration, or proximally, causing fibrosis. Using an unbiased microarray analysis, we found that digit tip regeneration is significantly associated with hair follicle differentiation, Wnt, and sonic hedgehog (SHH) signaling pathways. Viral over-expression and genetic knockouts showed the functional significance of these pathways during regeneration. Using transgenic reporter mice, we demonstrated that, while both canonical Wnt and HH signaling were limited to epidermal tissues, downstream hedgehog signaling (through Gli) occurred in mesenchymal tissues. These findings reveal a mechanism for epidermal/mesenchyme interactions, governed by canonical hedgehog signaling, during digit regeneration. Further research into these pathways could lead to improved therapeutic outcomes after hand injuries in humans. |
format | Online Article Text |
id | pubmed-8467649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84676492021-09-27 Epidermal-Derived Hedgehog Signaling Drives Mesenchymal Proliferation during Digit Tip Regeneration Maan, Zeshaan N. Rinkevich, Yuval Barrera, Janos Chen, Kellen Henn, Dominic Foster, Deshka Bonham, Clark Andrew Padmanabhan, Jagannath Sivaraj, Dharshan Duscher, Dominik Hu, Michael Yan, Kelley Januszyk, Michael Longaker, Michael T. Weissman, Irving L. Gurtner, Geoffrey C. J Clin Med Article Hand injuries often result in significant functional impairments and are rarely completely restored. The spontaneous regeneration of injured appendages, which occurs in salamanders and newts, for example, has been reported in human fingertips after distal amputation, but this type of regeneration is rare in mammals and is incompletely understood. Here, we study fingertip regeneration by amputating murine digit tips, either distally to initiate regeneration, or proximally, causing fibrosis. Using an unbiased microarray analysis, we found that digit tip regeneration is significantly associated with hair follicle differentiation, Wnt, and sonic hedgehog (SHH) signaling pathways. Viral over-expression and genetic knockouts showed the functional significance of these pathways during regeneration. Using transgenic reporter mice, we demonstrated that, while both canonical Wnt and HH signaling were limited to epidermal tissues, downstream hedgehog signaling (through Gli) occurred in mesenchymal tissues. These findings reveal a mechanism for epidermal/mesenchyme interactions, governed by canonical hedgehog signaling, during digit regeneration. Further research into these pathways could lead to improved therapeutic outcomes after hand injuries in humans. MDPI 2021-09-20 /pmc/articles/PMC8467649/ /pubmed/34575372 http://dx.doi.org/10.3390/jcm10184261 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Maan, Zeshaan N. Rinkevich, Yuval Barrera, Janos Chen, Kellen Henn, Dominic Foster, Deshka Bonham, Clark Andrew Padmanabhan, Jagannath Sivaraj, Dharshan Duscher, Dominik Hu, Michael Yan, Kelley Januszyk, Michael Longaker, Michael T. Weissman, Irving L. Gurtner, Geoffrey C. Epidermal-Derived Hedgehog Signaling Drives Mesenchymal Proliferation during Digit Tip Regeneration |
title | Epidermal-Derived Hedgehog Signaling Drives Mesenchymal Proliferation during Digit Tip Regeneration |
title_full | Epidermal-Derived Hedgehog Signaling Drives Mesenchymal Proliferation during Digit Tip Regeneration |
title_fullStr | Epidermal-Derived Hedgehog Signaling Drives Mesenchymal Proliferation during Digit Tip Regeneration |
title_full_unstemmed | Epidermal-Derived Hedgehog Signaling Drives Mesenchymal Proliferation during Digit Tip Regeneration |
title_short | Epidermal-Derived Hedgehog Signaling Drives Mesenchymal Proliferation during Digit Tip Regeneration |
title_sort | epidermal-derived hedgehog signaling drives mesenchymal proliferation during digit tip regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8467649/ https://www.ncbi.nlm.nih.gov/pubmed/34575372 http://dx.doi.org/10.3390/jcm10184261 |
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