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Nuclear morphometry and ploidy of normal and neoplastic haemocytes in mussels

Haemic neoplasia (HN) in bivalves has been reported in association with mass mortality events in various species of molluscs. The aim of this work was to quantify the nuclear morphometry and DNA content of neoplastic cells of mussels Mytilus galloprovincialis affected by HN using nuclear densitometr...

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Autores principales: Carella, Francesca, De Vico, Gionata, Landini, Gabriel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345825/
https://www.ncbi.nlm.nih.gov/pubmed/28282459
http://dx.doi.org/10.1371/journal.pone.0173219
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author Carella, Francesca
De Vico, Gionata
Landini, Gabriel
author_facet Carella, Francesca
De Vico, Gionata
Landini, Gabriel
author_sort Carella, Francesca
collection PubMed
description Haemic neoplasia (HN) in bivalves has been reported in association with mass mortality events in various species of molluscs. The aim of this work was to quantify the nuclear morphometry and DNA content of neoplastic cells of mussels Mytilus galloprovincialis affected by HN using nuclear densitometry in Feulgen-stained preparations. The results were also compared with a population of normal mussel haemocytes. We captured 256 images of 3 different neoplasia stages and 120 images of normal haemocytes; thus, a total of 120,166 nuclei were analysed. We extracted 21 morphological parameters from normal and neoplastic nuclei. Eighteen of these parameters were different (P<0.05). Among those (expressed in pixel units—inter-pixel distance of 0.45 micrometres—as: normal vs. neoplastic) nuclear area (117.1±94.1 vs. 423.1±226.9), perimeter (44.9±14.0 vs. 79.0±21.3) and (IOD) integrated optical density (13.47±34.5 vs. 177.1±150.8) were relevant features to discriminate between normal and neoplastic cells. Those differences allowed identifying two distinctive populations of neoplastic nuclei, occasionally in the same individuals at a given phase of the disease. Moreover, neoplastic haemocytes in less extended lesions showed a ploidy value of 6.2 n along with the presence of a second population of circulating cells with a DNA content of 10.7n. In samples with moderate disease only one peak at 7n was observed. Finally, in more severe conditions, a further ploidy peak of 7.8n was recorded, accompanied by a shallow but broad peak of 31n. This latter extreme value is thought to be due to the presence of giant multinucleated cells where individual nuclei overlap in space and cannot be discerned individually. Computer-based imaging allowed the direct visualization of the cell populations and simultaneous collection of ploidy data as well as morphological features of nuclei.
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spelling pubmed-53458252017-03-30 Nuclear morphometry and ploidy of normal and neoplastic haemocytes in mussels Carella, Francesca De Vico, Gionata Landini, Gabriel PLoS One Research Article Haemic neoplasia (HN) in bivalves has been reported in association with mass mortality events in various species of molluscs. The aim of this work was to quantify the nuclear morphometry and DNA content of neoplastic cells of mussels Mytilus galloprovincialis affected by HN using nuclear densitometry in Feulgen-stained preparations. The results were also compared with a population of normal mussel haemocytes. We captured 256 images of 3 different neoplasia stages and 120 images of normal haemocytes; thus, a total of 120,166 nuclei were analysed. We extracted 21 morphological parameters from normal and neoplastic nuclei. Eighteen of these parameters were different (P<0.05). Among those (expressed in pixel units—inter-pixel distance of 0.45 micrometres—as: normal vs. neoplastic) nuclear area (117.1±94.1 vs. 423.1±226.9), perimeter (44.9±14.0 vs. 79.0±21.3) and (IOD) integrated optical density (13.47±34.5 vs. 177.1±150.8) were relevant features to discriminate between normal and neoplastic cells. Those differences allowed identifying two distinctive populations of neoplastic nuclei, occasionally in the same individuals at a given phase of the disease. Moreover, neoplastic haemocytes in less extended lesions showed a ploidy value of 6.2 n along with the presence of a second population of circulating cells with a DNA content of 10.7n. In samples with moderate disease only one peak at 7n was observed. Finally, in more severe conditions, a further ploidy peak of 7.8n was recorded, accompanied by a shallow but broad peak of 31n. This latter extreme value is thought to be due to the presence of giant multinucleated cells where individual nuclei overlap in space and cannot be discerned individually. Computer-based imaging allowed the direct visualization of the cell populations and simultaneous collection of ploidy data as well as morphological features of nuclei. Public Library of Science 2017-03-10 /pmc/articles/PMC5345825/ /pubmed/28282459 http://dx.doi.org/10.1371/journal.pone.0173219 Text en © 2017 Carella et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are credited.
spellingShingle Research Article
Carella, Francesca
De Vico, Gionata
Landini, Gabriel
Nuclear morphometry and ploidy of normal and neoplastic haemocytes in mussels
title Nuclear morphometry and ploidy of normal and neoplastic haemocytes in mussels
title_full Nuclear morphometry and ploidy of normal and neoplastic haemocytes in mussels
title_fullStr Nuclear morphometry and ploidy of normal and neoplastic haemocytes in mussels
title_full_unstemmed Nuclear morphometry and ploidy of normal and neoplastic haemocytes in mussels
title_short Nuclear morphometry and ploidy of normal and neoplastic haemocytes in mussels
title_sort nuclear morphometry and ploidy of normal and neoplastic haemocytes in mussels
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345825/
https://www.ncbi.nlm.nih.gov/pubmed/28282459
http://dx.doi.org/10.1371/journal.pone.0173219
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