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Regeneration of reptilian scales after wounding: neogenesis, regional difference, and molecular modules
Lizard skin can produce scales during embryonic development, tail regeneration, and wound healing; however, underlying molecular signaling and extracellular matrix protein expression remains unknown. We mapped cell proliferation, signaling and extracellular matrix proteins in regenerating and develo...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961719/ https://www.ncbi.nlm.nih.gov/pubmed/24665362 http://dx.doi.org/10.1002/reg2.9 |
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author | Wu, Ping Alibardi, Lorenzo Chuong, Cheng‐Ming |
author_facet | Wu, Ping Alibardi, Lorenzo Chuong, Cheng‐Ming |
author_sort | Wu, Ping |
collection | PubMed |
description | Lizard skin can produce scales during embryonic development, tail regeneration, and wound healing; however, underlying molecular signaling and extracellular matrix protein expression remains unknown. We mapped cell proliferation, signaling and extracellular matrix proteins in regenerating and developing lizard scales in different body regions with different wound severity. Following lizard tail autotomy (self‐amputation), de novo scales regenerate from regenerating tail blastema. Despite topological differences between embryonic and adult scale formation, asymmetric cell proliferation produces the newly formed outer scale surface. Regionally different responses to wounding were observed; open wounds induced better scale regeneration from tail skin than trunk skin. Molecular studies suggest that neural cell adhesion molecule enriched dermal regions exhibit higher cell proliferation associated with scale growth. β‐catenin may be involved in epidermal scale differentiation. Dynamic tenascin‐C expression suggests its involvement in regeneration. We conclude that different skin regions exhibit different competence for de novo scale formation. While cellular and morphogenetic paths differ during development and regeneration of lizard scale formation, they share general proliferation patterns, epithelial−mesenchymal interactions and similar molecular modules composed of adhesion and extracellular matrix molecules. |
format | Online Article Text |
id | pubmed-3961719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-39617192015-02-01 Regeneration of reptilian scales after wounding: neogenesis, regional difference, and molecular modules Wu, Ping Alibardi, Lorenzo Chuong, Cheng‐Ming Regeneration (Oxf) Research Articles Lizard skin can produce scales during embryonic development, tail regeneration, and wound healing; however, underlying molecular signaling and extracellular matrix protein expression remains unknown. We mapped cell proliferation, signaling and extracellular matrix proteins in regenerating and developing lizard scales in different body regions with different wound severity. Following lizard tail autotomy (self‐amputation), de novo scales regenerate from regenerating tail blastema. Despite topological differences between embryonic and adult scale formation, asymmetric cell proliferation produces the newly formed outer scale surface. Regionally different responses to wounding were observed; open wounds induced better scale regeneration from tail skin than trunk skin. Molecular studies suggest that neural cell adhesion molecule enriched dermal regions exhibit higher cell proliferation associated with scale growth. β‐catenin may be involved in epidermal scale differentiation. Dynamic tenascin‐C expression suggests its involvement in regeneration. We conclude that different skin regions exhibit different competence for de novo scale formation. While cellular and morphogenetic paths differ during development and regeneration of lizard scale formation, they share general proliferation patterns, epithelial−mesenchymal interactions and similar molecular modules composed of adhesion and extracellular matrix molecules. John Wiley and Sons Inc. 2014-02-17 /pmc/articles/PMC3961719/ /pubmed/24665362 http://dx.doi.org/10.1002/reg2.9 Text en © 2014 The Authors. Regeneration published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/3.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Wu, Ping Alibardi, Lorenzo Chuong, Cheng‐Ming Regeneration of reptilian scales after wounding: neogenesis, regional difference, and molecular modules |
title | Regeneration of reptilian scales after wounding: neogenesis, regional difference, and molecular modules |
title_full | Regeneration of reptilian scales after wounding: neogenesis, regional difference, and molecular modules |
title_fullStr | Regeneration of reptilian scales after wounding: neogenesis, regional difference, and molecular modules |
title_full_unstemmed | Regeneration of reptilian scales after wounding: neogenesis, regional difference, and molecular modules |
title_short | Regeneration of reptilian scales after wounding: neogenesis, regional difference, and molecular modules |
title_sort | regeneration of reptilian scales after wounding: neogenesis, regional difference, and molecular modules |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961719/ https://www.ncbi.nlm.nih.gov/pubmed/24665362 http://dx.doi.org/10.1002/reg2.9 |
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