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Long-term time-lapse live imaging reveals extensive cell migration during annelid regeneration

BACKGROUND: Time-lapse imaging has proven highly valuable for studying development, yielding data of much finer resolution than traditional “still-shot” studies and allowing direct examination of tissue and cell dynamics. A major challenge for time-lapse imaging of animals is keeping specimens immob...

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Autores principales: Zattara, Eduardo E., Turlington, Kate W., Bely, Alexandra E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804569/
https://www.ncbi.nlm.nih.gov/pubmed/27006129
http://dx.doi.org/10.1186/s12861-016-0104-2
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author Zattara, Eduardo E.
Turlington, Kate W.
Bely, Alexandra E.
author_facet Zattara, Eduardo E.
Turlington, Kate W.
Bely, Alexandra E.
author_sort Zattara, Eduardo E.
collection PubMed
description BACKGROUND: Time-lapse imaging has proven highly valuable for studying development, yielding data of much finer resolution than traditional “still-shot” studies and allowing direct examination of tissue and cell dynamics. A major challenge for time-lapse imaging of animals is keeping specimens immobile yet healthy for extended periods of time. Although this is often feasible for embryos, the difficulty of immobilizing typically motile juvenile and adult stages remains a persistent obstacle to time-lapse imaging of post-embryonic development. RESULTS: Here we describe a new method for long-duration time-lapse imaging of adults of the small freshwater annelid Pristina leidyi and use this method to investigate its regenerative processes. Specimens are immobilized with tetrodotoxin, resulting in irreversible paralysis yet apparently normal regeneration, and mounted in agarose surrounded by culture water or halocarbon oil, to prevent dehydration but allowing gas exchange. Using this method, worms can be imaged continuously and at high spatial-temporal resolution for up to 5 days, spanning the entire regeneration process. We performed a fine-scale analysis of regeneration growth rate and characterized cell migration dynamics during early regeneration. Our studies reveal the migration of several putative cell types, including one strongly resembling published descriptions of annelid neoblasts, a cell type suggested to be migratory based on “still-shot” studies and long hypothesized to be linked to regenerative success in annelids. CONCLUSIONS: Combining neurotoxin-based paralysis, live mounting techniques and a starvation-tolerant study system has allowed us to obtain the most extensive high-resolution longitudinal recordings of full anterior and posterior regeneration in an invertebrate, and to detect and characterize several cell types undergoing extensive migration during this process. We expect the tetrodotoxin paralysis and time-lapse imaging methods presented here to be broadly useful in studying other animals and of particular value for studying post-embryonic development. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12861-016-0104-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-48045692016-03-24 Long-term time-lapse live imaging reveals extensive cell migration during annelid regeneration Zattara, Eduardo E. Turlington, Kate W. Bely, Alexandra E. BMC Dev Biol Methodology Article BACKGROUND: Time-lapse imaging has proven highly valuable for studying development, yielding data of much finer resolution than traditional “still-shot” studies and allowing direct examination of tissue and cell dynamics. A major challenge for time-lapse imaging of animals is keeping specimens immobile yet healthy for extended periods of time. Although this is often feasible for embryos, the difficulty of immobilizing typically motile juvenile and adult stages remains a persistent obstacle to time-lapse imaging of post-embryonic development. RESULTS: Here we describe a new method for long-duration time-lapse imaging of adults of the small freshwater annelid Pristina leidyi and use this method to investigate its regenerative processes. Specimens are immobilized with tetrodotoxin, resulting in irreversible paralysis yet apparently normal regeneration, and mounted in agarose surrounded by culture water or halocarbon oil, to prevent dehydration but allowing gas exchange. Using this method, worms can be imaged continuously and at high spatial-temporal resolution for up to 5 days, spanning the entire regeneration process. We performed a fine-scale analysis of regeneration growth rate and characterized cell migration dynamics during early regeneration. Our studies reveal the migration of several putative cell types, including one strongly resembling published descriptions of annelid neoblasts, a cell type suggested to be migratory based on “still-shot” studies and long hypothesized to be linked to regenerative success in annelids. CONCLUSIONS: Combining neurotoxin-based paralysis, live mounting techniques and a starvation-tolerant study system has allowed us to obtain the most extensive high-resolution longitudinal recordings of full anterior and posterior regeneration in an invertebrate, and to detect and characterize several cell types undergoing extensive migration during this process. We expect the tetrodotoxin paralysis and time-lapse imaging methods presented here to be broadly useful in studying other animals and of particular value for studying post-embryonic development. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12861-016-0104-2) contains supplementary material, which is available to authorized users. BioMed Central 2016-03-23 /pmc/articles/PMC4804569/ /pubmed/27006129 http://dx.doi.org/10.1186/s12861-016-0104-2 Text en © Zattara 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 Methodology Article
Zattara, Eduardo E.
Turlington, Kate W.
Bely, Alexandra E.
Long-term time-lapse live imaging reveals extensive cell migration during annelid regeneration
title Long-term time-lapse live imaging reveals extensive cell migration during annelid regeneration
title_full Long-term time-lapse live imaging reveals extensive cell migration during annelid regeneration
title_fullStr Long-term time-lapse live imaging reveals extensive cell migration during annelid regeneration
title_full_unstemmed Long-term time-lapse live imaging reveals extensive cell migration during annelid regeneration
title_short Long-term time-lapse live imaging reveals extensive cell migration during annelid regeneration
title_sort long-term time-lapse live imaging reveals extensive cell migration during annelid regeneration
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804569/
https://www.ncbi.nlm.nih.gov/pubmed/27006129
http://dx.doi.org/10.1186/s12861-016-0104-2
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