Cargando…

Skeletal regeneration in the brittle star Amphiura filiformis

BACKGROUND: Brittle stars regenerate their whole arms post-amputation. Amphiura filiformis can now be used for molecular characterization of arm regeneration due to the availability of transcriptomic data. Previous work showed that specific developmental transcription factors known to take part in e...

Descripción completa

Detalles Bibliográficos
Autores principales: Czarkwiani, Anna, Ferrario, Cinzia, Dylus, David Viktor, Sugni, Michela, Oliveri, Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4841056/
https://www.ncbi.nlm.nih.gov/pubmed/27110269
http://dx.doi.org/10.1186/s12983-016-0149-x
_version_ 1782428339615563776
author Czarkwiani, Anna
Ferrario, Cinzia
Dylus, David Viktor
Sugni, Michela
Oliveri, Paola
author_facet Czarkwiani, Anna
Ferrario, Cinzia
Dylus, David Viktor
Sugni, Michela
Oliveri, Paola
author_sort Czarkwiani, Anna
collection PubMed
description BACKGROUND: Brittle stars regenerate their whole arms post-amputation. Amphiura filiformis can now be used for molecular characterization of arm regeneration due to the availability of transcriptomic data. Previous work showed that specific developmental transcription factors known to take part in echinoderm skeletogenesis are expressed during adult arm regeneration in A. filiformis; however, the process of skeleton formation remained poorly understood. Here, we present the results of an in-depth microscopic analysis of skeletal morphogenesis during regeneration, using calcein staining, EdU labeling and in situ hybridization. RESULTS: To better compare different samples, we propose a staging system for the early A. filiformis arm regeneration stages based on morphological landmarks identifiable in living animals and supported by histological analysis. We show that the calcified spicules forming the endoskeleton first appear very early during regeneration in the dermal layer of regenerates. These spicules then mature into complex skeletal elements of the differentiated arm during late regeneration. The mesenchymal cells in the dermal area express the skeletal marker genes Afi-c-lectin, Afi-p58b and Afi-p19; however, EdU labeling shows that these dermal cells do not proliferate. CONCLUSIONS: A. filiformis arms regenerate through a consistent set of developmental stages using a distalization-intercalation mode, despite variability in regeneration rate. Skeletal elements form in a mesenchymal cell layer that does not proliferate and thus must be supplied from a different source. Our work provides the basis for future cellular and molecular studies of skeleton regeneration in brittle stars. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12983-016-0149-x) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4841056
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-48410562016-04-23 Skeletal regeneration in the brittle star Amphiura filiformis Czarkwiani, Anna Ferrario, Cinzia Dylus, David Viktor Sugni, Michela Oliveri, Paola Front Zool Research BACKGROUND: Brittle stars regenerate their whole arms post-amputation. Amphiura filiformis can now be used for molecular characterization of arm regeneration due to the availability of transcriptomic data. Previous work showed that specific developmental transcription factors known to take part in echinoderm skeletogenesis are expressed during adult arm regeneration in A. filiformis; however, the process of skeleton formation remained poorly understood. Here, we present the results of an in-depth microscopic analysis of skeletal morphogenesis during regeneration, using calcein staining, EdU labeling and in situ hybridization. RESULTS: To better compare different samples, we propose a staging system for the early A. filiformis arm regeneration stages based on morphological landmarks identifiable in living animals and supported by histological analysis. We show that the calcified spicules forming the endoskeleton first appear very early during regeneration in the dermal layer of regenerates. These spicules then mature into complex skeletal elements of the differentiated arm during late regeneration. The mesenchymal cells in the dermal area express the skeletal marker genes Afi-c-lectin, Afi-p58b and Afi-p19; however, EdU labeling shows that these dermal cells do not proliferate. CONCLUSIONS: A. filiformis arms regenerate through a consistent set of developmental stages using a distalization-intercalation mode, despite variability in regeneration rate. Skeletal elements form in a mesenchymal cell layer that does not proliferate and thus must be supplied from a different source. Our work provides the basis for future cellular and molecular studies of skeleton regeneration in brittle stars. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12983-016-0149-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-22 /pmc/articles/PMC4841056/ /pubmed/27110269 http://dx.doi.org/10.1186/s12983-016-0149-x Text en © Czarkwiani et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Czarkwiani, Anna
Ferrario, Cinzia
Dylus, David Viktor
Sugni, Michela
Oliveri, Paola
Skeletal regeneration in the brittle star Amphiura filiformis
title Skeletal regeneration in the brittle star Amphiura filiformis
title_full Skeletal regeneration in the brittle star Amphiura filiformis
title_fullStr Skeletal regeneration in the brittle star Amphiura filiformis
title_full_unstemmed Skeletal regeneration in the brittle star Amphiura filiformis
title_short Skeletal regeneration in the brittle star Amphiura filiformis
title_sort skeletal regeneration in the brittle star amphiura filiformis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4841056/
https://www.ncbi.nlm.nih.gov/pubmed/27110269
http://dx.doi.org/10.1186/s12983-016-0149-x
work_keys_str_mv AT czarkwianianna skeletalregenerationinthebrittlestaramphiurafiliformis
AT ferrariocinzia skeletalregenerationinthebrittlestaramphiurafiliformis
AT dylusdavidviktor skeletalregenerationinthebrittlestaramphiurafiliformis
AT sugnimichela skeletalregenerationinthebrittlestaramphiurafiliformis
AT oliveripaola skeletalregenerationinthebrittlestaramphiurafiliformis