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Collective cell migration: leadership, invasion and segregation

Alexandre J. Kabla
Published 25 July 2012.DOI: 10.1098/rsif.2012.0448
Alexandre J. Kabla
Department of Engineering, University of Cambridge, Cambridge CB2 1PZ, UK
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      Figure 1.

      (a) An image of a motile tissue in the steady state, overlayed with the corresponding velocity field. Cell colours are arbitrary. (b) Maps of the velocity correlations around a cell migrating from left to right (see §3). These have been obtained for populations of 1600 cells. The unit distance is the cell diameter. (c) A graph of the correlation length Embedded Image as a function of the motile force μ, for J = 5.

    • Figure 2.
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      Figure 2.

      (a) Average mean-square displacement as a function of time for a range of motile force μ and adhesion J. The background colour reflects the value of Embedded Image, as represented on the x-axis of figure 2b. Distances are in pixels, and time is expressed in MCS (see §3), Embedded Image MCS. The dashed lines illustrate two limit behaviours corresponding to purely diffusive Embedded Image: slope 1) and purely ballistic (Embedded Image: slope 2) displacements, in order to facilitate the interpretation of the graphs. (b) A graph of the diffusion exponent β as a function of Embedded Image, for four different values of J (2.5, red; 5, yellow; 7.5, green; 10, blue). The vertical dashed line indicates the typical value of Embedded Image at which the epithelium to collective migration transition occurs.

    • Figure 3.
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      Figure 3.

      (a,b) Heat maps of the order parameter Embedded Image as a function of (a) μ and the system size Embedded Image (number of cells: Embedded Image) or (b) μ and the typical distance between leaders Embedded Image (in cell diameters). Data for three different values of J are presented. The dashed lines indicate the value of the motile force at which the Embedded Image is maximal. (c) An example of a tissue with a few leader cells (with pink/orange tone) whose polarity is constant and directed towards the right. (d) A sketch of the curve Embedded Image and its qualitative relationship with the different regimes of migration. For a given length scale d associated with a constraint (distance between leaders, distance between boundaries or number N of cells in the group (Embedded Image)), three regimes can be defined as μ increases: epithelium, sheet migration or uncoordinated.

    • Figure 4.
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      Figure 4.

      (a) Diffusion exponent β of a single motile cell in a tissue of non-motile cells. Embedded Image is determined by Embedded Image. Inset: mean-square displacement of single motile cells. (b) A graph of the total invasion distance Λ as a function of vt, where v is the mean speed of the tumour cells; this scaling compensates for the fact that the invasion rate trivially scales with v for Embedded Image. Data are shown for various motile forces (J = 5).

    • Figure 5.
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      Figure 5.

      (a) Evolution of Embedded Image (the number of contacts between two motile cells divided by the number of contacts between motile and non motile cells) for different motile forces μ (J = 5). The data have been obtained on a system of 2048 motile cells and 2048 non-motile cells. Inset: the same data are used to plot Embedded Image at different times. (b) A snapshot of the segregating tissue at t = 106 MCS with Embedded Image and J = 5.

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    7 December 2012
    Volume 9, issue 77
    • Table of Contents
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    Keywords

    collective migration
    epithelium
    wound healing
    cell invasion
    active matter
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    Collective cell migration: leadership, invasion and segregation
    Alexandre J. Kabla
    J. R. Soc. Interface 2012 9 3268-3278; DOI: 10.1098/rsif.2012.0448. Published 25 October 2012
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    Collective cell migration: leadership, invasion and segregation

    Alexandre J. Kabla
    J. R. Soc. Interface 2012 9 3268-3278; DOI: 10.1098/rsif.2012.0448. Published 25 October 2012

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