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

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          Abstract

          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.

          Abstract

          A new computational method allows researchers to measure the properties of individual nuclei in situations in which cells are tightly packed together, for example, during differentiation of stem cells in culture or during early postimplantation development.

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          Most cited references57

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          Theory of Edge Detection

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            Reconstitution of the mouse germ cell specification pathway in culture by pluripotent stem cells.

            The generation of properly functioning gametes in vitro requires reconstitution of the multistepped pathway of germ cell development. We demonstrate here the generation of primordial germ cell-like cells (PGCLCs) in mice with robust capacity for spermatogenesis. PGCLCs were generated from embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) through epiblast-like cells (EpiLCs), a cellular state highly similar to pregastrulating epiblasts but distinct from epiblast stem cells (EpiSCs). Reflecting epiblast development, EpiLC induction from ESCs/iPSCs is a progressive process, and EpiLCs highly competent for the PGC fate are a transient entity. The global transcription profiles, epigenetic reprogramming, and cellular dynamics during PGCLC induction from EpiLCs meticulously capture those associated with PGC specification from the epiblasts. Furthermore, we identify Integrin-β3 and SSEA1 as markers that allow the isolation of PGCLCs with spermatogenic capacity from tumorigenic undifferentiated cells. Our findings provide a paradigm for the first step of in vitro gametogenesis. Copyright © 2011 Elsevier Inc. All rights reserved.
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              Metadata matters: access to image data in the real world

              Data sharing is important in the biological sciences to prevent duplication of effort, to promote scientific integrity, and to facilitate and disseminate scientific discovery. Sharing requires centralized repositories, and submission to and utility of these resources require common data formats. This is particularly challenging for multidimensional microscopy image data, which are acquired from a variety of platforms with a myriad of proprietary file formats (PFFs). In this paper, we describe an open standard format that we have developed for microscopy image data. We call on the community to use open image data standards and to insist that all imaging platforms support these file formats. This will build the foundation for an open image data repository.
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                Author and article information

                Contributors
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: Funding acquisitionRole: InvestigationRole: MethodologyRole: Project administrationRole: ResourcesRole: SoftwareRole: SupervisionRole: ValidationRole: VisualizationRole: Writing – original draftRole: Writing – review & editing
                Role: Investigation
                Role: Investigation
                Role: Investigation
                Role: Validation
                Role: Data curationRole: Funding acquisitionRole: Project administrationRole: ResourcesRole: SupervisionRole: Writing – original draftRole: Writing – review & editing
                Role: Academic Editor
                Journal
                PLoS Biol
                PLoS Biol
                plos
                plosbiol
                PLoS Biology
                Public Library of Science (San Francisco, CA USA )
                1544-9173
                1545-7885
                9 August 2019
                August 2019
                9 August 2019
                : 17
                : 8
                : e3000388
                Affiliations
                [001]MRC Centre for Regenerative Medicine, Institute for Stem Cell Research, School of Biological Sciences, University of Edinburgh, Edinburgh, United Kingdom
                University of Dundee, UNITED KINGDOM
                Author notes

                The authors have declared that no competing interests exist.

                [¤]

                Current address: Sir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom

                Author information
                http://orcid.org/0000-0002-9295-237X
                http://orcid.org/0000-0001-7139-7314
                http://orcid.org/0000-0002-2350-7627
                http://orcid.org/0000-0002-4018-9480
                Article
                PBIOLOGY-D-19-00151
                10.1371/journal.pbio.3000388
                6703695
                31398189
                369b7c16-d253-4fa7-acf4-3c84e7cf1264
                © 2019 Blin et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 17 January 2019
                : 2 July 2019
                Page count
                Figures: 7, Tables: 0, Pages: 29
                Funding
                Funded by: funder-id http://dx.doi.org/10.13039/100004440, Wellcome Trust;
                Award ID: WT103789AIA
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/100004440, Wellcome Trust;
                Award ID: WT100133
                Award Recipient :
                This work was funded by a Wellcome Trust Senior Fellowship to SL (WT103789AIA) and a Wellcome Trust Sir Henry Wellcome Fellowship to GB (WT100133). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Methods and Resources
                Biology and Life Sciences
                Developmental Biology
                Embryology
                Embryos
                Biology and Life Sciences
                Developmental Biology
                Cell Differentiation
                Research and Analysis Methods
                Imaging Techniques
                Biology and Life Sciences
                Cell Biology
                Cell Processes
                Cell Cycle and Cell Division
                Biology and Life Sciences
                Biochemistry
                Proteins
                Protein Domains
                Sry Box
                Biology and Life Sciences
                Plant Science
                Plant Anatomy
                Leaves
                Research and Analysis Methods
                Imaging Techniques
                Computer Imaging
                Biology and Life Sciences
                Developmental Biology
                Morphogenesis
                Morphogenic Segmentation
                Custom metadata
                vor-update-to-uncorrected-proof
                2019-08-21
                Our imaging dataset DISCEPTS has been deposited to the Image Data Resource https://idr.openmicroscopy.org (Williams et al. 2017) under accession number idr0062. Data tables listing individual measurements used for figure charts are publicly available on GitLab ( https://framagit.org/pickcellslab/data/2019_nessys).

                Life sciences
                Life sciences

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