Nessys: A new set of tools for the automated detection of nuclei within intact tissues and dense 3D cultures.

Methods for measuring the properties of individual cells within their native 3D environment will enable a deeper understanding of embryonic development, tissue regeneration, and tumorigenesis. However, current methods for segmenting nuclei in 3D tissues are not designed for situations in which nucle...

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Main Authors: Guillaume Blin, Daina Sadurska, Rosa Portero Migueles, Naiming Chen, Julia A Watson, Sally Lowell
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-08-01
Series:PLoS Biology
Online Access:https://doi.org/10.1371/journal.pbio.3000388
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spelling doaj-25a6ea08c30f41bfab5aa919492d34572021-07-02T16:25:51ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852019-08-01178e300038810.1371/journal.pbio.3000388Nessys: A new set of tools for the automated detection of nuclei within intact tissues and dense 3D cultures.Guillaume BlinDaina SadurskaRosa Portero MiguelesNaiming ChenJulia A WatsonSally LowellMethods for measuring the properties of individual cells within their native 3D environment will enable a deeper understanding of embryonic development, tissue regeneration, and tumorigenesis. However, current methods for segmenting nuclei in 3D tissues are not designed for situations in which nuclei are densely packed, nonspherical, or heterogeneous in shape, size, or texture, all of which are true of many embryonic and adult tissue types as well as in many cases for cells differentiating in culture. Here, we overcome this bottleneck by devising a novel method based on labelling the nuclear envelope (NE) and automatically distinguishing individual nuclei using a tree-structured ridge-tracing method followed by shape ranking according to a trained classifier. The method is fast and makes it possible to process images that are larger than the computer's memory. We consistently obtain accurate segmentation rates of >90%, even for challenging images such as mid-gestation embryos or 3D cultures. We provide a 3D editor and inspector for the manual curation of the segmentation results as well as a program to assess the accuracy of the segmentation. We have also generated a live reporter of the NE that can be used to track live cells in 3 dimensions over time. We use this to monitor the history of cell interactions and occurrences of neighbour exchange within cultures of pluripotent cells during differentiation. We provide these tools in an open-access user-friendly format.https://doi.org/10.1371/journal.pbio.3000388
collection DOAJ
language English
format Article
sources DOAJ
author Guillaume Blin
Daina Sadurska
Rosa Portero Migueles
Naiming Chen
Julia A Watson
Sally Lowell
spellingShingle Guillaume Blin
Daina Sadurska
Rosa Portero Migueles
Naiming Chen
Julia A Watson
Sally Lowell
Nessys: A new set of tools for the automated detection of nuclei within intact tissues and dense 3D cultures.
PLoS Biology
author_facet Guillaume Blin
Daina Sadurska
Rosa Portero Migueles
Naiming Chen
Julia A Watson
Sally Lowell
author_sort Guillaume Blin
title Nessys: A new set of tools for the automated detection of nuclei within intact tissues and dense 3D cultures.
title_short Nessys: A new set of tools for the automated detection of nuclei within intact tissues and dense 3D cultures.
title_full Nessys: A new set of tools for the automated detection of nuclei within intact tissues and dense 3D cultures.
title_fullStr Nessys: A new set of tools for the automated detection of nuclei within intact tissues and dense 3D cultures.
title_full_unstemmed Nessys: A new set of tools for the automated detection of nuclei within intact tissues and dense 3D cultures.
title_sort nessys: a new set of tools for the automated detection of nuclei within intact tissues and dense 3d cultures.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2019-08-01
description Methods for measuring the properties of individual cells within their native 3D environment will enable a deeper understanding of embryonic development, tissue regeneration, and tumorigenesis. However, current methods for segmenting nuclei in 3D tissues are not designed for situations in which nuclei are densely packed, nonspherical, or heterogeneous in shape, size, or texture, all of which are true of many embryonic and adult tissue types as well as in many cases for cells differentiating in culture. Here, we overcome this bottleneck by devising a novel method based on labelling the nuclear envelope (NE) and automatically distinguishing individual nuclei using a tree-structured ridge-tracing method followed by shape ranking according to a trained classifier. The method is fast and makes it possible to process images that are larger than the computer's memory. We consistently obtain accurate segmentation rates of >90%, even for challenging images such as mid-gestation embryos or 3D cultures. We provide a 3D editor and inspector for the manual curation of the segmentation results as well as a program to assess the accuracy of the segmentation. We have also generated a live reporter of the NE that can be used to track live cells in 3 dimensions over time. We use this to monitor the history of cell interactions and occurrences of neighbour exchange within cultures of pluripotent cells during differentiation. We provide these tools in an open-access user-friendly format.
url https://doi.org/10.1371/journal.pbio.3000388
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