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Morphological investigations of posttraumatic regeneration in Timarete cf. punctata (Annelida: Cirratulidae)
INTRODUCTION: Annelids exhibit great regenerative abilities, which are mainly used after injury or during reproduction. These lophotrochozoans thus represent excellent models for regeneration research. However, detailed morphological studies concerning annelid musculature and nervous system redevelo...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657251/ https://www.ncbi.nlm.nih.gov/pubmed/26605065 http://dx.doi.org/10.1186/s40851-015-0023-2 |
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author | Weidhase, Michael Helm, Conrad Bleidorn, Christoph |
author_facet | Weidhase, Michael Helm, Conrad Bleidorn, Christoph |
author_sort | Weidhase, Michael |
collection | PubMed |
description | INTRODUCTION: Annelids exhibit great regenerative abilities, which are mainly used after injury or during reproduction. These lophotrochozoans thus represent excellent models for regeneration research. However, detailed morphological studies concerning annelid musculature and nervous system redevelopment are limited to few taxa, and do not allow for broader comparisons and general conclusions regarding common patterns amongst annelids. RESULTS: Using immunohistochemical staining combined with confocal laser scanning microscopy (cLSM), we investigated the redevelopment of body wall musculature and nervous system during anterior and posterior posttraumatic regeneration in Timarete cf. punctata. Both regeneration processes start with wound healing, blastema formation, and blastema patterning. In posterior regeneration, this leads to the development of a new pygidium and a segment addition zone (SAZ) anterior to this structure. New segments are subsequently added in a sequential fashion. Anterior regeneration in contrast shows the formation of a new prostomium and peristomium first, followed by the simultaneous redevelopment of three segments, and an additional three segments in sequential order. Anterior muscular regeneration shows an outgrowth of longitudinal musculature from the residual body wall musculature, while circular musculature develops independently within the blastema. During posterior regeneration, new musculature becomes visible when the new segments reached a certain age. Neuronal regeneration begins with neurite outgrowth from the old ventral nerve cord in both cases, which are later forming loop structures. In anterior regeneration, the brain redevelops at the anteriormost position of the loops. CONCLUSIONS: Posterior regeneration recapitulates normal growth from a certain timepoint with serial segment development by a posterior segment addition zone. Anterior regeneration is more complex, showing similarities to larval development in matters of the order, in which prostomium, peristomium, and segments are generated. Furthermore, we demonstrate the usefulness of regeneration studies to investigate morphological structures and evolutionary processes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40851-015-0023-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4657251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46572512015-11-24 Morphological investigations of posttraumatic regeneration in Timarete cf. punctata (Annelida: Cirratulidae) Weidhase, Michael Helm, Conrad Bleidorn, Christoph Zoological Lett Research Article INTRODUCTION: Annelids exhibit great regenerative abilities, which are mainly used after injury or during reproduction. These lophotrochozoans thus represent excellent models for regeneration research. However, detailed morphological studies concerning annelid musculature and nervous system redevelopment are limited to few taxa, and do not allow for broader comparisons and general conclusions regarding common patterns amongst annelids. RESULTS: Using immunohistochemical staining combined with confocal laser scanning microscopy (cLSM), we investigated the redevelopment of body wall musculature and nervous system during anterior and posterior posttraumatic regeneration in Timarete cf. punctata. Both regeneration processes start with wound healing, blastema formation, and blastema patterning. In posterior regeneration, this leads to the development of a new pygidium and a segment addition zone (SAZ) anterior to this structure. New segments are subsequently added in a sequential fashion. Anterior regeneration in contrast shows the formation of a new prostomium and peristomium first, followed by the simultaneous redevelopment of three segments, and an additional three segments in sequential order. Anterior muscular regeneration shows an outgrowth of longitudinal musculature from the residual body wall musculature, while circular musculature develops independently within the blastema. During posterior regeneration, new musculature becomes visible when the new segments reached a certain age. Neuronal regeneration begins with neurite outgrowth from the old ventral nerve cord in both cases, which are later forming loop structures. In anterior regeneration, the brain redevelops at the anteriormost position of the loops. CONCLUSIONS: Posterior regeneration recapitulates normal growth from a certain timepoint with serial segment development by a posterior segment addition zone. Anterior regeneration is more complex, showing similarities to larval development in matters of the order, in which prostomium, peristomium, and segments are generated. Furthermore, we demonstrate the usefulness of regeneration studies to investigate morphological structures and evolutionary processes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40851-015-0023-2) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-06 /pmc/articles/PMC4657251/ /pubmed/26605065 http://dx.doi.org/10.1186/s40851-015-0023-2 Text en © Weidhase et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Article Weidhase, Michael Helm, Conrad Bleidorn, Christoph Morphological investigations of posttraumatic regeneration in Timarete cf. punctata (Annelida: Cirratulidae) |
title | Morphological investigations of posttraumatic regeneration in Timarete cf. punctata (Annelida: Cirratulidae) |
title_full | Morphological investigations of posttraumatic regeneration in Timarete cf. punctata (Annelida: Cirratulidae) |
title_fullStr | Morphological investigations of posttraumatic regeneration in Timarete cf. punctata (Annelida: Cirratulidae) |
title_full_unstemmed | Morphological investigations of posttraumatic regeneration in Timarete cf. punctata (Annelida: Cirratulidae) |
title_short | Morphological investigations of posttraumatic regeneration in Timarete cf. punctata (Annelida: Cirratulidae) |
title_sort | morphological investigations of posttraumatic regeneration in timarete cf. punctata (annelida: cirratulidae) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657251/ https://www.ncbi.nlm.nih.gov/pubmed/26605065 http://dx.doi.org/10.1186/s40851-015-0023-2 |
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