8
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Bridging from single to collective cell migration: A review of models and links to experiments

      review-article
      * ,
      PLoS Computational Biology
      Public Library of Science

      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

          Mathematical and computational models can assist in gaining an understanding of cell behavior at many levels of organization. Here, we review models in the literature that focus on eukaryotic cell motility at 3 size scales: intracellular signaling that regulates cell shape and movement, single cell motility, and collective cell behavior from a few cells to tissues. We survey recent literature to summarize distinct computational methods (phase-field, polygonal, Cellular Potts, and spherical cells). We discuss models that bridge between levels of organization, and describe levels of detail, both biochemical and geometric, included in the models. We also highlight links between models and experiments. We find that models that span the 3 levels are still in the minority.

          Author summary

          In this review paper, we summarize the literature on computational models for cell motility, from the biochemical networks that regulate it, to the behavior of 1 and many cells. We discuss the distinct approaches used at each level, and how models can build bridges between the different size scales. We find models at many different levels of biological detail, and discuss their relative contributions to our understanding of single and collective cell behavior. Finally, we indicate how models have been linked to biological experiments in this field.

          Related collections

          Most cited references182

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

          Collective cell migration in morphogenesis, regeneration and cancer.

          The collective migration of cells as a cohesive group is a hallmark of the tissue remodelling events that underlie embryonic morphogenesis, wound repair and cancer invasion. In such migration, cells move as sheets, strands, clusters or ducts rather than individually, and use similar actin- and myosin-mediated protrusions and guidance by extrinsic chemotactic and mechanical cues as used by single migratory cells. However, cadherin-based junctions between cells additionally maintain 'supracellular' properties, such as collective polarization, force generation, decision making and, eventually, complex tissue organization. Comparing different types of collective migration at the molecular and cellular level reveals a common mechanistic theme between developmental and cancer research.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Sniffers, buzzers, toggles and blinkers: dynamics of regulatory and signaling pathways in the cell.

            The physiological responses of cells to external and internal stimuli are governed by genes and proteins interacting in complex networks whose dynamical properties are impossible to understand by intuitive reasoning alone. Recent advances by theoretical biologists have demonstrated that molecular regulatory networks can be accurately modeled in mathematical terms. These models shed light on the design principles of biological control systems and make predictions that have been verified experimentally.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Cell movement is guided by the rigidity of the substrate.

              Directional cell locomotion is critical in many physiological processes, including morphogenesis, the immune response, and wound healing. It is well known that in these processes cell movements can be guided by gradients of various chemical signals. In this study, we demonstrate that cell movement can also be guided by purely physical interactions at the cell-substrate interface. We cultured National Institutes of Health 3T3 fibroblasts on flexible polyacrylamide sheets coated with type I collagen. A transition in rigidity was introduced in the central region of the sheet by a discontinuity in the concentration of the bis-acrylamide cross-linker. Cells approaching the transition region from the soft side could easily migrate across the boundary, with a concurrent increase in spreading area and traction forces. In contrast, cells migrating from the stiff side turned around or retracted as they reached the boundary. We call this apparent preference for a stiff substrate "durotaxis." In addition to substrate rigidity, we discovered that cell movement could also be guided by manipulating the flexible substrate to produce mechanical strains in the front or rear of a polarized cell. We conclude that changes in tissue rigidity and strain could play an important controlling role in a number of normal and pathological processes involving cell locomotion.
                Bookmark

                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Comput Biol
                PLoS Comput Biol
                plos
                ploscomp
                PLoS Computational Biology
                Public Library of Science (San Francisco, CA USA )
                1553-734X
                1553-7358
                December 2020
                10 December 2020
                : 16
                : 12
                : e1008411
                Affiliations
                [001] Department of Mathematics, University of British Columbia, Vancouver, Canada
                New York University, UNITED STATES
                Author notes

                The authors have declared that no competing interests exist.

                Author information
                https://orcid.org/0000-0002-4943-7591
                https://orcid.org/0000-0002-2233-690X
                Article
                PCOMPBIOL-D-20-01106
                10.1371/journal.pcbi.1008411
                7728230
                33301528
                6a7b92bc-8360-4a8e-8d1a-9ff6a189cfdc
                © 2020 Buttenschön, Edelstein-Keshet

                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
                Page count
                Figures: 5, Tables: 2, Pages: 34
                Funding
                AB and LEK are supported by an NSERC [Discovery Grant 41870 to LEK]. AB was partially supported by a NSERC PDF Fellowship. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Review
                Biology and Life Sciences
                Biochemistry
                Enzymology
                Enzymes
                Hydrolases
                Guanosine Triphosphatase
                Biology and Life Sciences
                Biochemistry
                Proteins
                Enzymes
                Hydrolases
                Guanosine Triphosphatase
                Biology and Life Sciences
                Cell Biology
                Cell Motility
                Cell Migration
                Biology and Life Sciences
                Developmental Biology
                Cell Migration
                Biology and life sciences
                Cell biology
                Signal transduction
                Cell signaling
                GTPase signaling
                Biology and Life Sciences
                Cell Biology
                Cell Motility
                Biology and Life Sciences
                Cell Biology
                Signal Transduction
                Cell Signaling
                Biology and Life Sciences
                Cell Biology
                Cell Physiology
                Cell Polarity
                Biology and Life Sciences
                Biochemistry
                Proteins
                Contractile Proteins
                Actins
                Biology and Life Sciences
                Biochemistry
                Proteins
                Cytoskeletal Proteins
                Actins
                Computer and Information Sciences
                Network Analysis
                Signaling Networks

                Quantitative & Systems biology
                Quantitative & Systems biology

                Comments

                Comment on this article