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Live Imaging of Axolotl Digit Regeneration Reveals Spatiotemporal Choreography of Diverse Connective Tissue Progenitor Pools

Connective tissues—skeleton, dermis, pericytes, fascia—are a key cell source for regenerating the patterned skeleton during axolotl appendage regeneration. This complexity has made it difficult to identify the cells that regenerate skeletal tissue. Inability to identify these cells has impeded a mec...

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Detalles Bibliográficos
Autores principales: Currie, Joshua D., Kawaguchi, Akane, Traspas, Ricardo Moreno, Schuez, Maritta, Chara, Osvaldo, Tanaka, Elly M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5127896/
https://www.ncbi.nlm.nih.gov/pubmed/27840105
http://dx.doi.org/10.1016/j.devcel.2016.10.013
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author Currie, Joshua D.
Kawaguchi, Akane
Traspas, Ricardo Moreno
Schuez, Maritta
Chara, Osvaldo
Tanaka, Elly M.
author_facet Currie, Joshua D.
Kawaguchi, Akane
Traspas, Ricardo Moreno
Schuez, Maritta
Chara, Osvaldo
Tanaka, Elly M.
author_sort Currie, Joshua D.
collection PubMed
description Connective tissues—skeleton, dermis, pericytes, fascia—are a key cell source for regenerating the patterned skeleton during axolotl appendage regeneration. This complexity has made it difficult to identify the cells that regenerate skeletal tissue. Inability to identify these cells has impeded a mechanistic understanding of blastema formation. By tracing cells during digit tip regeneration using brainbow transgenic axolotls, we show that cells from each connective tissue compartment have distinct spatial and temporal profiles of proliferation, migration, and differentiation. Chondrocytes proliferate but do not migrate into the regenerate. In contrast, pericytes proliferate, then migrate into the blastema and give rise solely to pericytes. Periskeletal cells and fibroblasts contribute the bulk of digit blastema cells and acquire diverse fates according to successive waves of migration that choreograph their proximal-distal and tissue contributions. We further show that platelet-derived growth factor signaling is a potent inducer of fibroblast migration, which is required to form the blastema.
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spelling pubmed-51278962016-12-06 Live Imaging of Axolotl Digit Regeneration Reveals Spatiotemporal Choreography of Diverse Connective Tissue Progenitor Pools Currie, Joshua D. Kawaguchi, Akane Traspas, Ricardo Moreno Schuez, Maritta Chara, Osvaldo Tanaka, Elly M. Dev Cell Article Connective tissues—skeleton, dermis, pericytes, fascia—are a key cell source for regenerating the patterned skeleton during axolotl appendage regeneration. This complexity has made it difficult to identify the cells that regenerate skeletal tissue. Inability to identify these cells has impeded a mechanistic understanding of blastema formation. By tracing cells during digit tip regeneration using brainbow transgenic axolotls, we show that cells from each connective tissue compartment have distinct spatial and temporal profiles of proliferation, migration, and differentiation. Chondrocytes proliferate but do not migrate into the regenerate. In contrast, pericytes proliferate, then migrate into the blastema and give rise solely to pericytes. Periskeletal cells and fibroblasts contribute the bulk of digit blastema cells and acquire diverse fates according to successive waves of migration that choreograph their proximal-distal and tissue contributions. We further show that platelet-derived growth factor signaling is a potent inducer of fibroblast migration, which is required to form the blastema. Cell Press 2016-11-21 /pmc/articles/PMC5127896/ /pubmed/27840105 http://dx.doi.org/10.1016/j.devcel.2016.10.013 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Currie, Joshua D.
Kawaguchi, Akane
Traspas, Ricardo Moreno
Schuez, Maritta
Chara, Osvaldo
Tanaka, Elly M.
Live Imaging of Axolotl Digit Regeneration Reveals Spatiotemporal Choreography of Diverse Connective Tissue Progenitor Pools
title Live Imaging of Axolotl Digit Regeneration Reveals Spatiotemporal Choreography of Diverse Connective Tissue Progenitor Pools
title_full Live Imaging of Axolotl Digit Regeneration Reveals Spatiotemporal Choreography of Diverse Connective Tissue Progenitor Pools
title_fullStr Live Imaging of Axolotl Digit Regeneration Reveals Spatiotemporal Choreography of Diverse Connective Tissue Progenitor Pools
title_full_unstemmed Live Imaging of Axolotl Digit Regeneration Reveals Spatiotemporal Choreography of Diverse Connective Tissue Progenitor Pools
title_short Live Imaging of Axolotl Digit Regeneration Reveals Spatiotemporal Choreography of Diverse Connective Tissue Progenitor Pools
title_sort live imaging of axolotl digit regeneration reveals spatiotemporal choreography of diverse connective tissue progenitor pools
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5127896/
https://www.ncbi.nlm.nih.gov/pubmed/27840105
http://dx.doi.org/10.1016/j.devcel.2016.10.013
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