Cargando…

An amputation resets positional information to a proximal identity in the regenerating zebrafish caudal fin

BACKGROUND: Zebrafish has emerged as a powerful model organism to study the process of regeneration. This teleost fish has the ability to regenerate various tissues and organs like the heart, spinal cord, retina and fins. In this study, we took advantage of the existence of an excellent morphologica...

Descripción completa

Detalles Bibliográficos
Autores principales: Azevedo, Ana Sofia, Sousa, Sara, Jacinto, António, Saúde, Leonor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3484062/
https://www.ncbi.nlm.nih.gov/pubmed/22920534
http://dx.doi.org/10.1186/1471-213X-12-24
_version_ 1782248092674818048
author Azevedo, Ana Sofia
Sousa, Sara
Jacinto, António
Saúde, Leonor
author_facet Azevedo, Ana Sofia
Sousa, Sara
Jacinto, António
Saúde, Leonor
author_sort Azevedo, Ana Sofia
collection PubMed
description BACKGROUND: Zebrafish has emerged as a powerful model organism to study the process of regeneration. This teleost fish has the ability to regenerate various tissues and organs like the heart, spinal cord, retina and fins. In this study, we took advantage of the existence of an excellent morphological reference in the zebrafish caudal fin, the bony ray bifurcations, as a model to study positional information upon amputation. We investigated the existence of positional information for bifurcation formation by performing repeated amputations at different proximal-distal places along the fin. RESULTS: We show that, while amputations performed at a long distance from the bifurcation do not change its final proximal-distal position in the regenerated fin, consecutive amputations done at 1 segment proximal to the bifurcation (near the bifurcation) induce a positional reset and progressively shift its position distally. Furthermore, we investigated the potential role of Shh and Fgf signalling pathways in the determination of the bifurcation position and observed that they do not seem to be involved in this process. CONCLUSIONS: Our results reveal that, an amputation near the bifurcation inhibits the formation of the regenerated bifurcation in the pre-amputation position, inducing a distalization of this structure. This shows that the positional memory for bony ray bifurcations depends on the proximal-distal level of the amputation.
format Online
Article
Text
id pubmed-3484062
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-34840622012-10-31 An amputation resets positional information to a proximal identity in the regenerating zebrafish caudal fin Azevedo, Ana Sofia Sousa, Sara Jacinto, António Saúde, Leonor BMC Dev Biol Research Article BACKGROUND: Zebrafish has emerged as a powerful model organism to study the process of regeneration. This teleost fish has the ability to regenerate various tissues and organs like the heart, spinal cord, retina and fins. In this study, we took advantage of the existence of an excellent morphological reference in the zebrafish caudal fin, the bony ray bifurcations, as a model to study positional information upon amputation. We investigated the existence of positional information for bifurcation formation by performing repeated amputations at different proximal-distal places along the fin. RESULTS: We show that, while amputations performed at a long distance from the bifurcation do not change its final proximal-distal position in the regenerated fin, consecutive amputations done at 1 segment proximal to the bifurcation (near the bifurcation) induce a positional reset and progressively shift its position distally. Furthermore, we investigated the potential role of Shh and Fgf signalling pathways in the determination of the bifurcation position and observed that they do not seem to be involved in this process. CONCLUSIONS: Our results reveal that, an amputation near the bifurcation inhibits the formation of the regenerated bifurcation in the pre-amputation position, inducing a distalization of this structure. This shows that the positional memory for bony ray bifurcations depends on the proximal-distal level of the amputation. BioMed Central 2012-08-25 /pmc/articles/PMC3484062/ /pubmed/22920534 http://dx.doi.org/10.1186/1471-213X-12-24 Text en Copyright ©2012 Azevedo et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Azevedo, Ana Sofia
Sousa, Sara
Jacinto, António
Saúde, Leonor
An amputation resets positional information to a proximal identity in the regenerating zebrafish caudal fin
title An amputation resets positional information to a proximal identity in the regenerating zebrafish caudal fin
title_full An amputation resets positional information to a proximal identity in the regenerating zebrafish caudal fin
title_fullStr An amputation resets positional information to a proximal identity in the regenerating zebrafish caudal fin
title_full_unstemmed An amputation resets positional information to a proximal identity in the regenerating zebrafish caudal fin
title_short An amputation resets positional information to a proximal identity in the regenerating zebrafish caudal fin
title_sort amputation resets positional information to a proximal identity in the regenerating zebrafish caudal fin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3484062/
https://www.ncbi.nlm.nih.gov/pubmed/22920534
http://dx.doi.org/10.1186/1471-213X-12-24
work_keys_str_mv AT azevedoanasofia anamputationresetspositionalinformationtoaproximalidentityintheregeneratingzebrafishcaudalfin
AT sousasara anamputationresetspositionalinformationtoaproximalidentityintheregeneratingzebrafishcaudalfin
AT jacintoantonio anamputationresetspositionalinformationtoaproximalidentityintheregeneratingzebrafishcaudalfin
AT saudeleonor anamputationresetspositionalinformationtoaproximalidentityintheregeneratingzebrafishcaudalfin
AT azevedoanasofia amputationresetspositionalinformationtoaproximalidentityintheregeneratingzebrafishcaudalfin
AT sousasara amputationresetspositionalinformationtoaproximalidentityintheregeneratingzebrafishcaudalfin
AT jacintoantonio amputationresetspositionalinformationtoaproximalidentityintheregeneratingzebrafishcaudalfin
AT saudeleonor amputationresetspositionalinformationtoaproximalidentityintheregeneratingzebrafishcaudalfin