Cargando…

The periosteal requirement and temporal dynamics of BMP2‐induced middle phalanx regeneration in the adult mouse

Regeneration of mammalian limbs is restricted to amputation of the distal digit tip, the terminal phalanx (P3). The adjacent skeletal element, the middle phalanx (P2), has emerged as a model system to investigate regenerative failure and as a site to test approaches aimed at enhancing regeneration....

Descripción completa

Detalles Bibliográficos
Autores principales: Dawson, Lindsay A., Yu, Ling, Yan, Mingquan, Marrero, Luis, Schanes, Paula P., Dolan, Connor, Pela, Maegan, Petersen, Britta, Han, Manjong, Muneoka, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617898/
https://www.ncbi.nlm.nih.gov/pubmed/28975034
http://dx.doi.org/10.1002/reg2.81
_version_ 1783267064382750720
author Dawson, Lindsay A.
Yu, Ling
Yan, Mingquan
Marrero, Luis
Schanes, Paula P.
Dolan, Connor
Pela, Maegan
Petersen, Britta
Han, Manjong
Muneoka, Ken
author_facet Dawson, Lindsay A.
Yu, Ling
Yan, Mingquan
Marrero, Luis
Schanes, Paula P.
Dolan, Connor
Pela, Maegan
Petersen, Britta
Han, Manjong
Muneoka, Ken
author_sort Dawson, Lindsay A.
collection PubMed
description Regeneration of mammalian limbs is restricted to amputation of the distal digit tip, the terminal phalanx (P3). The adjacent skeletal element, the middle phalanx (P2), has emerged as a model system to investigate regenerative failure and as a site to test approaches aimed at enhancing regeneration. We report that exogenous application of bone morphogenetic protein 2 (BMP2) stimulates the formation of a transient cartilaginous callus distal to the amputation plane that mediates the regeneration of the amputated P2 bone. BMP2 initiates a significant regeneration response during the periosteal‐derived cartilaginous healing phase of P2 bone repair, yet fails to induce regeneration in the absence of periosteal tissue, or after boney callus formation. We provide evidence that a temporal component exists in the induced regeneration of P2 that we define as the “regeneration window.” In this window, cells are transiently responsive to BMP2 after the amputation injury. Simple re‐injury of the healed P2 stump acts to reinitiate endogenous bone repair, complete with periosteal chondrogenesis, thus reopening the “regeneration window” and thereby recreating a regeneration‐permissive environment that is responsive to exogenous BMP2 treatment.
format Online
Article
Text
id pubmed-5617898
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-56178982017-10-03 The periosteal requirement and temporal dynamics of BMP2‐induced middle phalanx regeneration in the adult mouse Dawson, Lindsay A. Yu, Ling Yan, Mingquan Marrero, Luis Schanes, Paula P. Dolan, Connor Pela, Maegan Petersen, Britta Han, Manjong Muneoka, Ken Regeneration (Oxf) Research Articles Regeneration of mammalian limbs is restricted to amputation of the distal digit tip, the terminal phalanx (P3). The adjacent skeletal element, the middle phalanx (P2), has emerged as a model system to investigate regenerative failure and as a site to test approaches aimed at enhancing regeneration. We report that exogenous application of bone morphogenetic protein 2 (BMP2) stimulates the formation of a transient cartilaginous callus distal to the amputation plane that mediates the regeneration of the amputated P2 bone. BMP2 initiates a significant regeneration response during the periosteal‐derived cartilaginous healing phase of P2 bone repair, yet fails to induce regeneration in the absence of periosteal tissue, or after boney callus formation. We provide evidence that a temporal component exists in the induced regeneration of P2 that we define as the “regeneration window.” In this window, cells are transiently responsive to BMP2 after the amputation injury. Simple re‐injury of the healed P2 stump acts to reinitiate endogenous bone repair, complete with periosteal chondrogenesis, thus reopening the “regeneration window” and thereby recreating a regeneration‐permissive environment that is responsive to exogenous BMP2 treatment. John Wiley and Sons Inc. 2017-08-20 /pmc/articles/PMC5617898/ /pubmed/28975034 http://dx.doi.org/10.1002/reg2.81 Text en © 2017 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/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Dawson, Lindsay A.
Yu, Ling
Yan, Mingquan
Marrero, Luis
Schanes, Paula P.
Dolan, Connor
Pela, Maegan
Petersen, Britta
Han, Manjong
Muneoka, Ken
The periosteal requirement and temporal dynamics of BMP2‐induced middle phalanx regeneration in the adult mouse
title The periosteal requirement and temporal dynamics of BMP2‐induced middle phalanx regeneration in the adult mouse
title_full The periosteal requirement and temporal dynamics of BMP2‐induced middle phalanx regeneration in the adult mouse
title_fullStr The periosteal requirement and temporal dynamics of BMP2‐induced middle phalanx regeneration in the adult mouse
title_full_unstemmed The periosteal requirement and temporal dynamics of BMP2‐induced middle phalanx regeneration in the adult mouse
title_short The periosteal requirement and temporal dynamics of BMP2‐induced middle phalanx regeneration in the adult mouse
title_sort periosteal requirement and temporal dynamics of bmp2‐induced middle phalanx regeneration in the adult mouse
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617898/
https://www.ncbi.nlm.nih.gov/pubmed/28975034
http://dx.doi.org/10.1002/reg2.81
work_keys_str_mv AT dawsonlindsaya theperiostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT yuling theperiostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT yanmingquan theperiostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT marreroluis theperiostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT schanespaulap theperiostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT dolanconnor theperiostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT pelamaegan theperiostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT petersenbritta theperiostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT hanmanjong theperiostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT muneokaken theperiostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT dawsonlindsaya periostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT yuling periostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT yanmingquan periostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT marreroluis periostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT schanespaulap periostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT dolanconnor periostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT pelamaegan periostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT petersenbritta periostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT hanmanjong periostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse
AT muneokaken periostealrequirementandtemporaldynamicsofbmp2inducedmiddlephalanxregenerationintheadultmouse