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Digit Tip Regeneration: Merging Regeneration Biology with Regenerative Medicine
Regeneration Biology is the study of organisms with endogenous regenerative abilities, whereas Regenerative Medicine focuses on engineering solutions for human injuries that do not regenerate. While the two fields are fundamentally different in their approach, there is an obvious interface involving...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5827737/ https://www.ncbi.nlm.nih.gov/pubmed/29405625 http://dx.doi.org/10.1002/sctm.17-0236 |
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author | Dolan, Connor P. Dawson, Lindsay A. Muneoka, Ken |
author_facet | Dolan, Connor P. Dawson, Lindsay A. Muneoka, Ken |
author_sort | Dolan, Connor P. |
collection | PubMed |
description | Regeneration Biology is the study of organisms with endogenous regenerative abilities, whereas Regenerative Medicine focuses on engineering solutions for human injuries that do not regenerate. While the two fields are fundamentally different in their approach, there is an obvious interface involving mammalian regeneration models. The fingertip is the only part of the human limb that is regeneration‐competent and the regenerating mouse digit tip has emerged as a model to study a clinically relevant regenerative response. In this article, we discuss how studies of digit tip regeneration have identified critical components of the regenerative response, and how an understanding of endogenous regeneration can lead to expanding the regenerative capabilities of nonregenerative amputation wounds. Such studies demonstrate that regeneration‐incompetent wounds can respond to treatment with individual morphogenetic agents by initiating a multi‐tissue response that culminates in structural regeneration. In addition, the healing process of nonregenerative wounds are found to cycle through nonresponsive, responsive and nonresponsive phases, and we call the responsive phase the Regeneration Window. We also find the responsiveness of mature healed amputation wounds can be reactivated by reinjury, thus nonregenerated wounds retain a potential for regeneration. We propose that regeneration‐incompetent injuries possess dormant regenerative potential that can be activated by targeted treatment with specific morphogenetic agents. We believe that future Regenerative Medicine‐based‐therapies should be designed to promote, not replace, regenerative responses. Stem Cells Translational Medicine 2018;7:262–270 |
format | Online Article Text |
id | pubmed-5827737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58277372018-03-01 Digit Tip Regeneration: Merging Regeneration Biology with Regenerative Medicine Dolan, Connor P. Dawson, Lindsay A. Muneoka, Ken Stem Cells Transl Med Perspectives Regeneration Biology is the study of organisms with endogenous regenerative abilities, whereas Regenerative Medicine focuses on engineering solutions for human injuries that do not regenerate. While the two fields are fundamentally different in their approach, there is an obvious interface involving mammalian regeneration models. The fingertip is the only part of the human limb that is regeneration‐competent and the regenerating mouse digit tip has emerged as a model to study a clinically relevant regenerative response. In this article, we discuss how studies of digit tip regeneration have identified critical components of the regenerative response, and how an understanding of endogenous regeneration can lead to expanding the regenerative capabilities of nonregenerative amputation wounds. Such studies demonstrate that regeneration‐incompetent wounds can respond to treatment with individual morphogenetic agents by initiating a multi‐tissue response that culminates in structural regeneration. In addition, the healing process of nonregenerative wounds are found to cycle through nonresponsive, responsive and nonresponsive phases, and we call the responsive phase the Regeneration Window. We also find the responsiveness of mature healed amputation wounds can be reactivated by reinjury, thus nonregenerated wounds retain a potential for regeneration. We propose that regeneration‐incompetent injuries possess dormant regenerative potential that can be activated by targeted treatment with specific morphogenetic agents. We believe that future Regenerative Medicine‐based‐therapies should be designed to promote, not replace, regenerative responses. Stem Cells Translational Medicine 2018;7:262–270 John Wiley and Sons Inc. 2018-02-05 /pmc/articles/PMC5827737/ /pubmed/29405625 http://dx.doi.org/10.1002/sctm.17-0236 Text en © 2018 The Authors Stem Cells Translational Medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Perspectives Dolan, Connor P. Dawson, Lindsay A. Muneoka, Ken Digit Tip Regeneration: Merging Regeneration Biology with Regenerative Medicine |
title | Digit Tip Regeneration: Merging Regeneration Biology with Regenerative Medicine |
title_full | Digit Tip Regeneration: Merging Regeneration Biology with Regenerative Medicine |
title_fullStr | Digit Tip Regeneration: Merging Regeneration Biology with Regenerative Medicine |
title_full_unstemmed | Digit Tip Regeneration: Merging Regeneration Biology with Regenerative Medicine |
title_short | Digit Tip Regeneration: Merging Regeneration Biology with Regenerative Medicine |
title_sort | digit tip regeneration: merging regeneration biology with regenerative medicine |
topic | Perspectives |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5827737/ https://www.ncbi.nlm.nih.gov/pubmed/29405625 http://dx.doi.org/10.1002/sctm.17-0236 |
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