28
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Using argument notation to engineer biological simulations with increased confidence

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The application of computational and mathematical modelling to explore the mechanics of biological systems is becoming prevalent. To significantly impact biological research, notably in developing novel therapeutics, it is critical that the model adequately represents the captured system. Confidence in adopting in silico approaches can be improved by applying a structured argumentation approach, alongside model development and results analysis. We propose an approach based on argumentation from safety-critical systems engineering, where a system is subjected to a stringent analysis of compliance against identified criteria. We show its use in examining the biological information upon which a model is based, identifying model strengths, highlighting areas requiring additional biological experimentation and providing documentation to support model publication. We demonstrate our use of structured argumentation in the development of a model of lymphoid tissue formation, specifically Peyer's Patches. The argumentation structure is captured using A rtoo (www.york.ac.uk/ycil/software/artoo), our Web-based tool for constructing fitness-for-purpose arguments, using a notation based on the safety-critical goal structuring notation. We show how argumentation helps in making the design and structured analysis of a model transparent, capturing the reasoning behind the inclusion or exclusion of each biological feature and recording assumptions, as well as pointing to evidence supporting model-derived conclusions.

          Related collections

          Most cited references1

          • Record: found
          • Abstract: found
          • Article: not found

          Compartmentalization of Peyer's patch anlagen before lymphocyte entry.

          We have shown that Peyer's patch (PP) first develops as a simple and even cell aggregation during embryogenesis. To investigate when and how such a simple cell aggregation forms the complex PP architecture, we analyzed the distribution of cells expressing IL-7R alpha (PP inducer cells), VCAM-1 (mesenchymal cells), CD11c (dendritic cells), and mature lymphocytes by whole-mount immunostaining of 17.5 days post coitus to 2 days postpartum mouse gut. Our results show that compartmentalization of PP anlagen commences at day 18.5 of gestation by clustering and subsequent follicle formation of IL-7R alpha(+), VCAM-1(+), and CD11c(+) cells. This process adds the primitive architecture of PP anlage with several follicles in which IL-7R alpha(+) cells localize in the center, while VCAM-1(+) and CD11c(+) cells localize at the fringe. This follicle formation is accompanied by the establishment of PP-specific vascular network expressing mucosal addressin cellular adhesion molecule-1. Mature B and T lymphocytes entering in the PP anlage are distributed promptly to their own target zones; B cells to the follicle and T cells to nonfollicular zones. Our analysis of scid/scid mouse indicate that the initial processes including formation of PP-specific vascular network occur in the absence of lymphocytes. These observations indicate that the basic architecture of PP is formed by a set of cell lineages assembled during the initial phase of induction of PP anlagen before entry of mature lymphocytes.
            Bookmark

            Author and article information

            Journal
            J R Soc Interface
            J R Soc Interface
            RSIF
            royinterface
            Journal of the Royal Society Interface
            The Royal Society
            1742-5689
            1742-5662
            6 March 2015
            6 March 2015
            : 12
            : 104
            : 20141059
            Affiliations
            [1 ]York Computational Immunology Laboratory, University of York , York, UK
            [2 ]Centre for Immunology and Infection, University of York , York, UK
            [3 ]Department of Computer Science, University of York , York, UK
            [4 ]York Centre for Complex Systems Analysis, University of York , York, UK
            [5 ]Department of Electronics, University of York , York, UK
            [6 ]Faculdade de Medicina de Lisboa, Instituto de Medicina Molecular , Lisboa, Portugal
            [7 ]SimOmics Ltd, The Catalyst , Baird Lane, Heslington, York, UK
            Author notes
            Article
            rsif20141059
            10.1098/rsif.2014.1059
            4345473
            25589574
            d9366862-af62-4cfb-8b3d-9272c7590804

            © 2015 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.

            History
            : 23 September 2014
            : 16 December 2014
            Categories
            1004
            44
            181
            Research Articles
            Custom metadata
            March 6, 2015

            Life sciences
            computational modelling,argumentation,simulation,artoo,immune system modelling
            Life sciences
            computational modelling, argumentation, simulation, artoo, immune system modelling

            Comments

            Comment on this article