# Adapting a Plant Tissue Model to Animal Development: Introducing Cell Sliding into VirtualLeaf

## Abstract

Cell-based, mathematical modeling of collective cell behavior has become a prominent tool in developmental biology. Cell-based models represent individual cells as single particles or as sets of interconnected particles and predict the collective cell behavior that follows from a set of interaction rules. In particular, vertex-based models are a popular tool for studying the mechanics of confluent, epithelial cell layers. They represent the junctions between three (or sometimes more) cells in confluent tissues as point particles, connected using structural elements that represent the cell boundaries. A disadvantage of these models is that cell–cell interfaces are represented as straight lines. This is a suitable simplification for epithelial tissues, where the interfaces are typically under tension, but this simplification may not be appropriate for mesenchymal tissues or tissues that are under compression, such that the cell–cell boundaries can buckle. In this paper, we introduce a variant of VMs in which this and two other limitations of VMs have been resolved. The new model can also be seen as on off-the-lattice generalization of the Cellular Potts Model. It is an extension of the open-source package VirtualLeaf, which was initially developed to simulate plant tissue morphogenesis where cells do not move relative to one another. The present extension of VirtualLeaf introduces a new rule for cell–cell shear or sliding, from which cell rearrangement (T1) and cell extrusion (T2) transitions emerge naturally, allowing the application of VirtualLeaf to problems of animal development. We show that the updated VirtualLeaf yields different results than the traditional vertex-based models for differential adhesion-driven cell sorting and for the neighborhood topology of soft cellular networks.

## Keywords

Cell-based modeling Vertex-based model Cellular Potts Model Developmental biology Epithelial tissues Junction remodeling Cell sorting Bubbly vertex model Cell rearrangement Epithelial morphogenesis## 1 Introduction

How cells form tissues, organs, and organisms remains one of the most intriguing and most central questions of biology. Recent theoretical approaches to study collective cell behavior are taking a prominent role in addressing these questions. Theoretical approaches provide deeper intuition about processes that typically are unfamiliar to the researchers by testing the physical plausibility of speculative hypotheses or by making predictions that can be tested experimentally. Theory can aid the analysis of data-rich time-lapse images of cell movements during development (Brodland et al. 2014; Merkel and Manning 2017) by simulating how the behavior of individual cells might lead to collective behavior and how collective movements might influence individual cell behaviors. To support theoretical analysis of tissue formation, a large range of mathematical methods have been proposed. These range from systems of partial differential equations models (see, e.g,. Keller and Segel 1970, 1971; Painter et al. 2015) to discrete methods that describe dense multicellular structures as interacting particle systems (see, e.g., Glazier and Graner 1993; Graner and Glazier 1992; Newman 2005; Sozinova et al. 2006; Voss-Böhme and Deutsch 2010; Woods et al. 2014; Smeets et al. 2016; Barton et al. 2017; Ghaffarizadeh et al. 2018 and Liedekerke et al. 2015 for review).

In contrast to continuum models, such so-called cell-based (Merks and Glazier 2005; Merks 2015) or single-cell-based methods (Anderson et al. 2007) have the disadvantage that formal dynamical analyses are impossible except in relatively simple cases (Voss-Böhme and Deutsch 2010). Nevertheless, in many biological applications cell-based models are preferred as they can incorporate ‘biological rules’ that reflect more physiologically realistic biology than can be achieved easily in continuum methods. For example, Odell et al. (1981) posed a calcium sensitive feedback system to spread a contraction wave. As developmental biologists adopt biophysical methods and borrow principles of control theory to explain tissue formation, simulations will need to capture interactions between multiple cell types and the diverse forms of cell–cell communication those interactions encode (Lander 2007). Models will further need to integrate structural, mechanical, and biochemical cues with downstream effectors of morphogenesis such as cell division, cell death events, and cell differentiation events (Maree and Hogeweg 2002; Hester et al. 2011; Boas et al. 2015; Palm et al. 2016). Cell-based simulation methods provide a rich framework to study multiscale phenomena such as these, in that they simulate the dynamics of the cell and the tissue as a whole, while subcellular dynamics can be naturally integrated, such as gene regulation, secretion of signaling molecules, the dynamics of the cytoskeleton, and electrophysiological mechanisms (Boas and Merks 2014; Belmonte et al. 2016; Sluka et al. 2016; Kudryashova et al. 2017). Thus, cell-based modeling approaches enable integration of the physics of collective cell behavior with diverse modes of subcellular biological regulation.

A large range of cell-based modeling techniques are available; they can be roughly classified into single-particle and multiparticle methods, and lattice-based and off-lattice techniques (Merks 2015). Single-particle techniques are efficient computationally and have found wide application, but they also have limitations. For example, cell shape can affect the outcome of cell–cell interactions: cells that mutually attract one another via a chemoattractant form network-like structures if they are elongated, while they form separate ‘islands’ if they are rounded (Merks et al. 2006). Also, it can be important that subcellular compartments interact with their local environment relatively independently from one another. For example, contact inhibition of cellular protrusions can promote directional migration of neural crest cells (Carmona-Fontaine et al. 2008). Although it is possible to simulate such problems using single-particle-based methods [see, e.g., Palachanis et al. (2015) for effects of cell shape in vascular patterning, Woods et al. (2014) for neural crest cell migration; and for cell sorting see, e.g., Sulsky et al. (1984); Graner and Sawada (1993); Osborne et al. (2017)], multiparticle methods allow for a large flexibility in cell shape that is more directly related to cell shapes acquired from time-lapse microscopy. Multiparticle methods are also better suited for the simulation of local mechanisms responsible for collective behavior (e.g., contact inhibition Woods et al. 2014), as they make it possible to reduce cell-level assumptions to subcellular mechanisms.

Two widely used multiparticle techniques for cell-based modeling include the Cellular Potts Model (CPM) and the vertex-based model (VM). The CPM represents cells as (usually connected) domains of lattice sites on a regular lattice. Cells move on the lattice by randomly extending or retracting their domain to adjacent lattice sites, according to a Hamiltonian energy function that describes the contractile and viscoelastic structures that form each cell, the physical adhesive interactions between cells, and in some cases, extracellular materials. Alternatively, structural elements have been used to describe the cell boundaries and cross-linking elements for the cell interior (Odell et al. 1981). A simplified version of this model is the vertex-based model (VM) (Weliky and Oster 1990; Honda et al. 1983; Staple et al. 2010). These represent the junctions between three (or sometimes more) cells in confluent tissues as point particles, connected using structural elements that represent the cell boundaries. Where the CPM defines tissues as assemblages of cells with individual cells represented as collections of adjacent lattice sites, VM describes the tissue as a polygonal tessellation of junctionally connected cells with each cell represented by a series of nodes representing three-cell junctions.

In principle, CPM and VM are equivalent. Like cells in CPMs, the dynamic movements of cells in VMs are driven by the physical properties of cell–cell interfaces, which are governed by a Hamiltonian function that usually includes interfacial tensions, cell adhesion, and cell area constraints. The parameters of CPM or VM can often be rescaled such that the model can be run in the other formalism (Magno et al. 2015). However, some cases can arise where the two modeling frameworks cannot be interconverted (Osborne et al. 2017). For instance, because the string-like elastic elements in their basic formulation describe cell–cell interfaces and require all cells to be interconnected, VMs are unsuitable for non-confluent tissues. In this paper, we discuss further limitations of traditional VMs including (a) description of cell–cell interfaces as straight lines, (b) separation of membrane fluctuations and model dynamics, and (c) algorithms that represent cell neighbor changes with rule-based T1 and T2 transitions.

In this paper, we introduce a variant of the VM in which these three limitations have been resolved. The model is an extension of the open-source package VirtualLeaf (Merks et al. 2011; Merks and Guravage 2012) (also see the re-engineered derivative *Virtual Plant Tissue*; De Vos et al. 2017), which was initially developed to simulate plant tissue morphogenesis where cells do not move relative to one another. VirtualLeaf differs from traditional VMs in that (a) cell interfaces are represented by multiple nodes that allow membrane fluctuations; (b) tissue topology changes exclusively through cell division with no T1 or T2 transitions; and (c) tissue dynamics are advanced used a Metropolis algorithm that incorporates membrane fluctuations. The present extension of VirtualLeaf introduces a new rule for cell–cell shear or sliding, from which T1 and T2 transitions emerge naturally, allowing the application of VirtualLeaf to problems of animal development.

We will discuss two cases for which the updated VirtualLeaf yields different results than traditional VM. First, we discuss simulations of differential adhesion-driven cell sorting and show that the new update rule for cell sliding facilitates complete cell sorting. We will then turn our attention to epithelial dynamics and discuss cases for which the flexibility of cell membranes affects the neighborhood topology of soft networks (Farhadifar et al. 2007).

## 2 Methods

*n*vertices, \(V_i=\{\mathbf {v}_1\dots \mathbf {v}_n\}\) that are connected by

*m*edges, \(E_i=\{\mathbf {e}_1 \ldots \mathbf {e}_m\}\), and a set of cell attributes, \(\alpha _i\). Adjacent cells share the same vertices and edges. Thus, the tissue \(T=\{C,V,E\}\) is defined by the set of all cells in the tissue,

*C*, and by all vertices in the tissue, \(V=\bigcup _{i\in T}V_i\) and all edges, \(E=\bigcup _{i\in T}E_i\) (Fig 1a). A Hamiltonian function,

*H*, describes the balance of passive, mechanical forces in the tissue, including adhesive forces between cells, membrane tensions, and expansive cellular forces. The exact form of the Hamiltonian differs between models; in its simplest form (Merks et al. 2011) it includes a volume conservation term to resist compression of the cells and a line tension term to resist expansion of the membranes,

*c*,

*i.e.*, the area it would take up in the absence of counteracting compressive or expansive forces,

*A*(

*c*), the actual area of cell

*c*, and \(\lambda _A\) is a Lagrange multiplier. The second RHS term gives the energy of the cell boundary, which is represented as a set of connected springs of rest length \(L_T\). The sum runs over the edges

*e*taken from

*E*, the set of all edges in the simulation, and \(\lambda _M\) is a Lagrange multiplier.

We update the model using Metropolis dynamics: We iteratively select a random node \(\mathbf {v}_i\) and attempt to move it to a randomly chosen new position \(\mathbf {v}^{\prime }_i=\mathbf {v}_i+\varvec{\xi }\varDelta x\), with \(\varvec{\xi }\in \{[-1/2,1/2],[-1/2,1/2]\}\), i.e., a random vector chosen uniformly from a square of size \(1\times 1\) centered at (0, 0), and \(\varDelta x\) the step size. The algorithm calculates the change of the Hamiltonian resulting from the attempt, \(\varDelta H\), and accepts the move if \(\varDelta H<0\). To keep the system from settling into local minima and to mimic active, random cell motility, we also accept moves increasing the Hamiltonian \(\varDelta H>0\) with Boltzmann probability \(P(\varDelta H)=\exp (-\varDelta H/T)\), with the Boltzmann temperature, *T*, setting the amount of random cell motility or ‘noise’ added in this way.

The key novelty that makes the model applicable to animal tissues is that here we allow cells to move through the tissue. To this end, we introduce a *sliding operator* to further reduce the Hamiltonian (Fig. 1c). The sliding operator allows a cell edge that is part of a tricellular or higher order junction to ‘hop’ to another vertex. For example an edge connecting nodes \(\mathbf {v}_1\) and \(\mathbf {v}_2\) can be moved to connect nodes \(\mathbf {v}_2\) and \(\mathbf {v}_3\). Similar to the regular moves, a slide is accepted with probability \(P(\varDelta H)=\{1,\varDelta H<0;\exp (-\varDelta H/T),\varDelta H>0\}\).

A single Monte Carlo Step (MCS) involves cycling over all nodes *v* in random order. For each node, we first attempt to move it. If the node is of order 3 or higher, we also try to slide it (see flowchart in Fig. 1f). After completion of one MCS, the descriptions of the cell membranes are refined if necessary, so as to keep an approximately even distribution of edge lengths. To do so, all edges \(\mathbf {e}\in E\) whose length exceeds a threshold, \(\Vert \mathbf {e}\Vert >l_\mathrm {max}\), are split into two by inserting a new vertex in the middle. Similarly, if \(\Vert \mathbf {e}\Vert <l_\mathrm {min}\), the edge is deleted from the tissue, replacing the two vertices and their connections for a new, fused vertex containing the connections of the two original vertices combined.

Independent of this Hamiltonian description of cell mechanics and cell motility, additional rules motivated by the biological problem can be included, including cell growth, cell division, and subcellular models describing the genetic or metabolic networks regulating cell behavior using differential equations (Merks et al. 2011). If the additional rules can be safely assumed to run at a much slower rate than the cellular mechanics, we make a quasi-steady state assumption for the cellular mechanics: First, we iterate the Metropolis dynamics until the Hamiltonian has practically stabilized, that is, if \(\varDelta H/\varDelta t<\epsilon \), with \(\epsilon \) a small number; then, we apply the additional rules for a number of time steps. In other models (i.e., the cell sorting model), the Metropolis algorithm describes a kinetic mechanism that does not stabilize within the course of a simulation. In those cases, we apply an operator splitting approach in which the Monte Carlo steps are alternated with steps of the additional rules.

## 3 Results

We validate the model extensions by looking at two classical problems: (a) differential adhesion cell sorting (Glazier and Graner 1993; Graner and Glazier 1992) and (b) cell packing in epithelial monolayers (Farhadifar et al. 2007). VirtualLeaf provides new insight into both problems.

### 3.1 Cell Sorting

Classic experiments by Holtfreter (reviewed in Steinberg 1996) have shown that cells of different embryonic tissues can phase separate. A number of closely related hypotheses have been proposed to explain this phenomenon. Steinberg (1963, 2007) has proposed the differential adhesion hypothesis. In this view, cell sorting is due to the interplay of differential adhesion and random cell motility, which progressively replaces weaker intercellular adhesions for stronger adhesions. In addition to differential adhesion, contraction of the cortical cytoskeleton contributes to the equilibrium configurations of mixed cell aggregates (Krieg et al. 2008), leading to the differential surface contraction (Harris 1976) aka differential interfacial tension (Brodland 2002) hypothesis.

Because of its importance for biological development and the possibility to predict the configuration corresponding with the energy minimum from the differential interfacial energies (Steinberg 1963), cell sorting has become a key benchmark problem for cell-based modeling methodology. Cell sorting has been reproduced in a practically all available cell-based models, including cellular automata (Antonelli et al. 1973), vertex-based models (Hutson et al. 2008), center-based models (Graner and Sawada 1993), and the Cellular Potts Model (Graner and Glazier 1992; Glazier and Graner 1993), but small differences are observed (Osborne et al. 2017): The kinetics of cell sorting differs between cell-based modeling methods as well as the extent to which the simulation gets trapped into local minima. Also, methodology relying on single particles to represent a cell may require unrealistically long interaction lengths or unrealistic cell motility models to achieve complete cell sorting (Osborne et al. 2017)

*A*(

*c*) and \(A_T (c)\) the actual area and resting areas of the cells. The adhesion energy is a sum over all edges \(\mathbf {e}\in E\) in the tissue, with parameter \(J(\mathbf {e}\rightarrow L,\mathbf {e}\rightarrow R)\) the adhesion energy per unit cell-cell interface separating the cell at the left (L) and the cell at the right (R) of the interface, where one cell can be the medium.

#### 3.1.1 Sliding Operator Enables Complete Cell Sorting

Figure 2a–c and Videos S1–S3 show the simulation results for three typical settings of the adhesion parameter J. The simulations are initiated with a configuration of \(20\times 20\) cells of size \(10\times 10\), with mixed or segregated cell type assignments as shown in the first column of Fig. 2. The target area is set equal to the initial area, at \(A_T=100\). The step size for the Monte Carlo algorithm is \(\varDelta x=0.5\), \(l_\mathrm {min}=6\), and \(l_\mathrm {max}=8\). For these parameter settings, the nodes are moved randomly over a square of side 1 / 20 of that of the initial length of the cell–cell interfaces, and one cell–cell interface consists typically of one to two edges, such that sliding moves occur over half to a full cell–cell interface.

In order to represent cell rearrangements, previous vertex-based simulations applied a rule-based T1 transitions. In these simulations, the T1 transition rearranges four adjacent cells as shown in Fig. 1b. The rule-based T1 transition is initiated if the length of an intercellular interface, i.e., an edge \(\mathbf {e}\) connecting a 3-connected node \(v_1\) with a second node \(v_2\), drops below a threshold, \(\Vert \mathbf {e}\Vert <\theta _\mathrm {T1}\). The T1 transition then deletes \(\mathbf {e}\) by fusing \(v_1\) and \(v_2\) and generates a new edge, \(\mathbf {e}_\perp \), perpendicular to \(\mathbf {e}\). In the absence of noise terms, vertex-based models based on such rule-based T1 transitions generally cannot achieve complete cell sorting, except in specific three-dimensional cases where almost complete cell sorting can be achieved (Hutson et al. 2008).

In the extended VirtualLeaf, T1 transitions are represented by a combination of two sliding moves, where both moves are driven by the Hamiltonian (Fig. 1c). As a first test of the extent to which the sliding operator changes the kinetics of cell sorting, in a second set of simulations we replaced it for rule-based T1 transitions. Figure 2d and Video S4 show a cell sorting experiment with only rule-based T1 transitions and a cellular temperature of \(T=10\), the same cellular temperature as that used in Fig. 2c. Without the sliding operator, cell sorting proceeds well over short times, with small clusters of green and red cells forming, but cell sorting remains incomplete. We have currently not investigated the causes of this in detail, but a potential factor is that the sliding operator is fully integrated in the energy minimization processes, in contrast to the rule-based treatment of T1 transitions. Also changing the threshold for rule-based T1 transitions, currently set at \(\theta _\mathrm {T1}=\varDelta x/2=0.25\), will likely speed up cell sorting. We will leave a full analysis of the sliding operator relative to the rule-based treatment of T1 transitions to future work.

#### 3.1.2 Differential Cortical Tension

As an experimental test of the differential adhesion hypothesis, Krieg and coworkers (Krieg et al. 2008) have measured the adhesive forces between induced germline progenitor cells from early zebrafish embryos. The heterotypic adhesion forces between induced endodermal, mesodermal, and ectodermal cells were approximately equal, whereas the homotypic adhesion forces differed between germ layers. Mesodermal cells adhered most strongly to one another, followed by endodermal cells, and ectodermal cells had the weakest adhesive forces to one another. Based on these data, the authors estimated relative values of the adhesion parameters, *J*, in a Cellular Potts Model. Strikingly, in the Zebrafish germline progenitor aggregates the least coherent ectodermal cells sorted to the middle of the cellular aggregates. This finding contradicts the differential adhesion hypothesis (DAH), which predicts that the least cohesive cells move to the aggregate’s periphery, see, e.g., the CPM (Graner and Glazier 1992) and our own simulations (Fig. 3, top-left to bottom-right diagonal). Krieg and coworkers demonstrated that the contradictory prediction can be attributed to differential cortical tension (DCT), an alternative to DAH (Harris 1976), with the highest cortical tension occurring at cell–medium interfaces. To implicitly incorporate cortical tension effects into the Cellular Potts Model, Krieg and coworkers reinterpreted the CPM such that a high value of *J* corresponded with a high interfacial tension.

*c*, and \(P_T (c)\), a target perimeter. Note that the cortical tension term was only applied at the cell–medium interfaces, which would be equivalent to setting \(\lambda _\mathrm {cortical}=0\) at cell–cell interfaces. The adhesion parameters were set such that \(J(r,r)<J(g,g)<J(g,r)\), i.e., red cells are more coherent than green cells, and red–green interfaces are energetically unfavorable. We have also assumed increased line tension at the boundary of the cell aggregate due to myosin activity (Krieg et al. 2008), by setting \(J(l,M)=0\) and \(J(d,M)=0\), but this has little effect on the results.

### 3.2 Epithelial Cell Packing

The structure of multicellular tissues and the shape of the constituent cells are driven by the interplay of cell division, cell growth, intercellular frictional forces, and global tissue mechanics. Epithelial tissues of plants (Kim et al. 2014) and of animals (Farhadifar et al. 2007) can be represented by two-dimensional tessellations and are, therefore, a popular model system for studying morphogenesis and emergence of tissue form (Lewis 1926). In particular, the number of neighbors in many epithelial tissues shows a characteristic distribution: Hexagonal cells are the most frequent, followed by pentagonal and heptagonal cells. Although the experimentally observed distribution can arise due to random cell division alone (Gibson et al. 2006), the biophysics of cell packing, i.e., programs of cell rearrangement and patterning of interfacial tensions, allows tissues to assume alternative, often narrower, i.e., more hexagonal neighbor distributions (Farhadifar et al. 2007). In the absence of cell rearrangements (as, e.g., in plant tissues), mathematical simulations have shown that cells must divide over the center of mass and the division plane must follow shortest paths, thus forming equally sized, symmetrically shaped daughter cells (Sahlin and Jönsson 2010).

#### 3.2.1 VirtualLeaf can Reproduce Key Features of Epithelial Cell Packing

Farhadifar et al. (2007) have shown that the cell packing deviates from these global equilibria if cell division is introduced. The authors picked one cell at random, doubled its target area, and relaxed the cellular configuration to the nearest equilibrium using a conjugate gradient method. They then divided the cell over a randomly oriented axis passing through the cell centroid, after which they relaxed the configuration again to its nearest equilibrium. This procedure was repeated until the tissue consisted of 10,000 cells, after which the topology of the tissue was examined.

After eight rounds of cell division, the distribution of polygon classes (\(P_n\), the fraction of polygons in the final tissue with *n* sides) in Case I agree, with only minor differences, with those reported in Farhadifar et al. (2007) (red bars in Fig. 4c). Both models reveal pentagon and hexagon-shaped cells dominate at \(P_5\approx 0.3\) and \(P_6\approx 0.3\) while heptagons are slightly less frequent at \(P_7\approx 0.2\), and tetragons and octagons are present at frequencies of \(P_4\approx P_8\approx 0.1\). Our model also has qualitative agreement in Case II and Case III with those reported for the vertex model although our model generated fewer 3-, 4-, 8-, and 9-sided cells. This difference can likely be attributed to the stochasticity in our simulations, which relaxes the configurations more quickly, similar to the effect of annealing reported in Farhadifar et al. (2007).

#### 3.2.2 Flexible Membranes and Sliding Change Case III, but not Cases I and II

We next tested whether membrane flexibility and the membrane sliding operator could replace algorithm-based T1 transitions to generate a topology indicative of growing tissues. We investigated the performance of these model innovations for three specific cases (Fig. 4b and Videos S11–S13). For Case I and Case II, the simulations in the presence of sliding and membrane flexibility showed no obvious differences with simulations of the vertex model. For Case I (Fig. 4c) and for Case II (Fig. 4d), the distribution of neighbor numbers did not differ between straight membranes (red and blue bars) and flexible membranes (yellow and green bars). Interestingly, for Case III both the visual appearance (Fig. 4b) and the neighbor distribution (Fig. 4e) were strongly affected in the presence of sliding and membrane flexibility (green bars): The number of heptagons was higher than for the other simulation conditions, and the number of pentagons was reduced. In the absence of membrane flexibility, sliding did not have this effect (blue bars), whereas for membrane flexibility and with T1 transitions, we observed only a small effect (yellow bars).

In Case I and Case II, the line tension (Case I) or cortical tension (Case II) straightens cell boundaries, such that boundary flexibility has no effect. In Case III, the specific topology of ‘soft networks’ is due to the boundaries’ resistance to compression by adjacent cells. Adding additional nodes to the membranes makes them flexible and allows membranes to buckle (see the ‘bubbly’ boundaries in Fig. 4b and Video S13, Case III), which will likely reduce the number of T1 transitions. We did not understand in detail why the distribution of neighbor numbers was particularly strongly affected in the presence of sliding. A potential explanation is that T1 transitions may introduce spurious energy barriers or time delays between configurations of higher and lower energy, consistent with the incomplete cell sorting discussed in Sect. 3.1.1, whereas for sliding such effects are reduced.

## 4 Discussion

In this paper, we have introduced extensions of our plant tissue simulation environment VirtualLeaf (Merks et al. 2011; Merks and Guravage 2012), adopting it for the simulation of animal tissues. The key novelty is a method to simulate relative movement of cells, the ‘sliding operator.’ This operator is applied alongside node displacements in a Metropolis-based energy minimization approach. We have validated the new model using simulations of differential adhesion-driven cell sorting and found that it can reproduce the key phenomena of differential adhesion-driven cell sorting, including cell mixing (Fig. 2a), engulfment of one cell type by the other (Fig. 2b), and cell sorting (Fig. 2c). The extended version of VirtualLeaf also reproduces the key phenomena of epithelial cell packing (Farhadifar et al. 2007) in ‘stiff’ regimes of the parameter space, i.e., in Cases I and II, where the cell perimeter is under tension (\(P(c)>P_T(c)\) and \(P_T(c)<2\sqrt{(}\pi A_T(c))\) (Fig. 4b–d). In the ‘soft’ parameter regime (Case III), i.e., if the cell perimeter is fully relaxed (\(P(c)=P_T(c)\) and \(P_T(c)>=2\sqrt{(}\pi A_T(c))\)), the results in VirtualLeaf differ from those reported previously (Farhadifar et al. 2007) due to buckling of the cell–cell interfaces.

The sliding operator requires that cell boundaries are represented by multiple nodes, between which an edge connecting 3 or more cells can ‘hop.’ Using the sliding operator, topological changes are entirely driven by the energy minimization process through at least two independent moves. In contrast, in traditional VMs, T1 transitions are initiated independently of the energy minimization process, as soon as the length of a cell–cell interface drops below a threshold. Because of this natural integration with the energy minimization algorithm, simulations with the sliding operator more quickly reached complete cell sorting (Fig. 2d) than our simulations with the traditional approach for T1 transitions. A full quantitative comparison of the two approaches will be left for the future work and will give more insight into the causes underlying these differences. For example, lowering the interface length threshold \(\theta _\mathrm {T1}\) for the T1 transitions will increase their frequency and will speed up cell sorting for simulations applying only T1 transitions. Similarly, in simulations applying the new slide operator, increasing the probability of slides and movements by increasing the Boltzmann temperature, *T*, increases the speed of cell sorting (Fig. 2e). Preliminary simulations with the new slide operator suggest that (perhaps somewhat counterintuitively) increasing the step size has little effect on the speed of cell sorting, because it affects only the node moves, but not the node slides that are responsible for cell rearrangement. Interestingly, our preliminary results suggest that increasing the number of nodes used per cell increases the speed of cell rearrangement (Video S14). A possible reason is that in the refined simulations energy barriers are more easily overcome: The smaller moves are associated with a lower, positive \(\varDelta H\). A full quantitative analysis of the effect of these and the other parameters on the biological behavior of our model and its computational efficiency will be left to the future work. This analysis will be necessary to decide on the appropriate application domain of this cell-based modeling method among alternative methodology (Osborne et al. 2017). As a first step, we plan to perform detailed comparisons with the CPM, which will require quantitative mapping of the model parameters in VirtualLeaf with those of the CPM. Such quantitative parameter mapping is available for the CPM and VMs (Magno et al. 2015), so these will form an excellent starting point.

Several cases of epithelial sheets have been observed to lack straight boundaries between cells including cells in the *Drosophila* amnioserosa (Toyama et al. 2008; Solon et al. 2009), cells surrounding the closing blastopore in *Xenopus* (Feroze et al. 2015), and the jigsaw puzzle cells of the plant epidermis (Fu et al. 2005; Carter et al. 2017; Sapala et al. 2018). Such irregular boundaries suggest tissue mechanics may be more complex than load-bearing by simple junctional tension (Salbreux et al. 2012). The deviations of cell–cell boundaries from simple lines imply that strain on these structures occurs both parallel and perpendicular to the junction. Deviations may reflect differential pressures between neighboring cells, the ability of the boundary to bend under compression (e.g., Euler buckling), or tensions perpendicular to the boundary. The presence of such irregular boundaries becomes more apparent when imaging tissues with higher magnification or when larger cells are sufficiently resolved by lower magnification objectives. The increasing discovery of such irregular-shaped cells has precipitated several innovations to VMs and related models (Fletcher et al. 2017). Bubbly vertex dynamics (Ishimoto and Morishita 2014) represents the cell–cell and cell–medium interfaces as curves instead of straight lines, where the curvature is due to pressure differences. This innovation changes the forces acting upon the vertices, and hence, it modifies the dynamics of the VM, but it does not allow buckling of cell boundaries. Buckling is possible thanks to our introduction of multiple cell–cell boundary elements between three cell junctions, which parallels similar innovations in VMs and related methods (Tamulonis et al. 2010; Tanaka et al. 2015; Perrone et al. 2016; Fletcher et al. 2017). These adaptations allow simulations of tissues that may experience anisotropic tensions or whose mechanics may be shaped by both medioapical cortical dynamics and junctional contractility. To better simulate such tissues, as a next step we will incorporate a bending stiffness [see, e.g., the bending stiffness of the perimeter in Barton et al. (2017)]. This will make it possible to explore the full parameter range between the maximally stiff, straight cell–cell interfaces in VMs, and the fully floppy cell–cell interfaces that we can currently represent in VirtualLeaf.

The Hamiltonian and the dynamics of VirtualLeaf (Merks et al. 2011) were inspired by both the Cellular Potts Model (Balter et al. 2007; Merks et al. 2011) and previous vertex-based models of plant tissue morphogenesis (Rudge and Haseloff 2005; Dupuy et al. 2008). The new sliding operator strengthens the similarity of the VirtualLeaf and the CPM, to the extent that our updated VirtualLeaf model can be seen as an ‘off-lattice’ version of the CPM. A related generalization of the CPM was introduced by Scianna and Preziosi (2016), who have introduced a node-based version of the CPMs. In this generalization, the cells can be represented on any tessellation, which has the advantage that the method can be interfaced with a wider range of methods for continuum mechanics where using arbitrary meshes is useful, e.g., for the finite-element method. The key innovation in their approach, which is shared with VirtualLeaf and VMs, is that cells are represented as polygons. This facilitates simulation of cortical cell tension. Unlike VirtualLeaf or the VM, the cell shapes in node-based CPM are constrained by a tessellation. This possibly introduces similar lattice effects as those found for the CPM, but an advantage of the approach is that it facilitates collision detection. Thus, like the standard CPM, the node-based CPM does not suffer from the limitation of VMs and VirtualLeaf that cell layers must be confluent. Future extensions, e.g., new operators for node fusions in conjunction with efficient collision detection algorithms, will relax those limitations of VirtualLeaf.

In conclusion, with the present extension of a sliding operator, we introduce a new multiparticle method for cell-based modeling and simulation. The method can be categorized within a continuum of closely related multiparticle, Hamiltonian-based methods ranging from lattice-based to off-latice methods. The CPM (Graner and Glazier 1992; Glazier and Graner 1993) is run on a regular lattice. The node-based CPM (Scianna and Preziosi 2016) can be run on irregular lattices. VirtualLeaf takes the CPM ‘off the lattice,’ with the current restriction that tissues must be confluent. Finally, the VM simplifies the representation of the tissue, by only representing tricellular junctions, connected by straight lines (Weliky and Oster 1990).

## Notes

## Supplementary material

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