|Study on multicellular systems using a phase field model.|
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|PMID: 22539943 Owner: NLM Status: MEDLINE|
|A model of multicellular systems with several types of cells is developed from the phase field model. The model is presented as a set of partial differential equations of the field variables, each of which expresses the shape of one cell. The dynamics of each cell is based on the criteria for minimizing the surface area and retaining a certain volume. The effects of cell adhesion and excluded volume are also taken into account. The proposed model can be used to find the position of the membrane and/or the cortex of each cell without the need to adopt extra variables. This model is suitable for numerical simulations of a system having a large number of cells. The two-dimensional results of cell division, cell adhesion, rearrangement of a cell cluster, chemotaxis, and cell sorting as well as the three-dimensional results of cell clusters on the substrate are presented.|
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|Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2012-04-23|
|Title: PloS one Volume: 7 ISSN: 1932-6203 ISO Abbreviation: PLoS ONE Publication Date: 2012|
|Created Date: 2012-04-27 Completed Date: 2012-09-10 Revised Date: 2013-06-25|
Medline Journal Info:
|Nlm Unique ID: 101285081 Medline TA: PLoS One Country: United States|
|Languages: eng Pagination: e33501 Citation Subset: IM|
|Department of Mathematical Information Engineering, College of Industrial Technology, Nihon University, Narashino-shi, Chiba, Japan. email@example.com|
|APA/MLA Format Download EndNote Download BibTex|
Cell Membrane / metabolism
Journal ID (nlm-ta): PLoS One
Journal ID (iso-abbrev): PLoS ONE
Journal ID (publisher-id): plos
Journal ID (pmc): plosone
Publisher: Public Library of Science, San Francisco, USA
Makiko Nonomura. 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.
Received Day: 15 Month: 9 Year: 2011
Accepted Day: 14 Month: 2 Year: 2012
collection publication date: Year: 2012
Electronic publication date: Day: 23 Month: 4 Year: 2012
Volume: 7 Issue: 4
E-location ID: e33501
PubMed Id: 22539943
Publisher Id: PONE-D-11-18137
|Study on Multicellular Systems Using a Phase Field Model Alternate Title:Multicellular Systems Using a Phase Field Model|
1Department of Mathematical Information Engineering, College of Industrial Technology, Nihon University, Narashino-shi, Chiba, Japan
2Japan Science and Technology Agency, PRESTO, Kawaguchi-shi, Saitama, Japan
|University of Georgia, United States of America
|Correspondence: * E-mail: firstname.lastname@example.org
Contributed by footnote: Conceived and designed the experiments: MN. Performed the experiments: MN. Analyzed the data: MN. Contributed reagents/materials/analysis tools: MN. Wrote the paper: MN.
In order to investigate the structural patterns of cellular systems, several cell models have been reported, including the vertex dynamics model , , the center dynamics model , , and the cellular Potts model , . Both the vertex dynamics model and the center dynamics model express cell patterns using polygons. In the vertex dynamics model, a cell or a cluster of cells is represented by a polygon formed by linking several vertices. Each vertex is driven by forces acting on it. This model has been adopted for morphogenesis in Xenopus notochords as well as cell deformation and rearrangement by applying mechanical forces , . In the center dynamics model, a node represents a cluster of cells and receives forces from its neighboring nodes. Cell aggregation, locomotion, rearrangement, and morphogenesis in vertebrate limb buds have been investigated using this model , , –. Although the mechanical processes during tissue developments can be well investigated, artificial treatments are required for numerical simulations in these models based on polygons. For example, in the vertex dynamics model, cell rearrangement is realized by manually exchanging two vertices that approach each other . In the center dynamics model, in order to express the cell division, it is necessary to add a new node in the vicinity of the existing node , .
In contrast, the cellular Potts model represents each cell as a cluster of grid points under the constraint of constant volume. Thus, the artificial treatments mentioned above are not required for simulations in this model. We can investigate the deformation of an individual cell in a multicellular system using this model, considering the effects of excluded volumes and adhesions of the cells. This model successfully described several biological behaviors . For example, numerical calculations with regard to cell sorting, biofilm formation, and chemotactic movement have been performed , , , . However, running the simulations requires fluctuations, and the forces between cells are not expressed directly in this model.
Therefore, we consider a new type of a model for multicellular systems, which is based on the phase field model. The effects of cell adhesion and excluded volume are taken into account. In the proposed model, the free energy is described in terms of a vector variable, the number of components of which is equivalent to the total number of cells in the system. The shape of one cell is expressed by one component of the vector variable. The time evolutions are described by a set of partial differential equations that are obtained by taking the functional derivative of the free energy. Thus, fluctuations are not required for numerical simulations. In addition, by adopting auxiliary variables that are used for calculation of the interactions between the cells, a program that consumes little computational memory can be designed. That is to say, the proposed model can be used to describe a system containing a large number of cells. The proposed model differs from previous models of multicellular systems in that the position of the cell membrane and/or cortex can also be expressed without the need to adopt extra variables because the phase boundary interface is treated as a diffuse interface of finite width using the phase field method.
The phase field model has been applied to a wide range of problems, such as crystal growth –. Very recently, the cell shape of the fish keratocyte has been modeled using this method, where the membrane bending force and the surface tension of the cell were considered . However, to our knowledge, this is the first report applying the phase field method to the multicellular system.
We consider a multicellular system containing several types of cells and allow changes in the size and adhesive strength of each cell type. As a first step, we express the shape of one cell using the phase field method.
The phase field model is based on the following Ginzburg-Landau free energy:denotes the area of the system, and the coefficient is a positive constant. The variable is an order parameter referred to as the phase field, where is the position, and t is the time. The function is given as is defined as and under the condition As shown in Figure 1, the depths of the wells are controlled by the constants and which correspond the free energy densities for the phases described by and respectively.
By taking the functional derivative of Equation 1 with respect to the time evolution of is derived as follows:is a positive constant and Equation 4 guarantees the monotonic decrease in the free energy. Equation 4 is referred to as the Allen–Cahn equation in the field of materials science and is known for having a smooth front solution connecting the regions and The Allen–Cahn equation can easily be solved in one dimension as where the front velocity This means that the front moves such that the region of expands if i.e.,
In order to describe a cell shape by the variable the constraint of the constant volume of should be included in Equation 4. When the volume of the region in which is denoted by the function , it is easy to consider this constraint by replacing the constant in Equation 4 with the following function :and are positive constants. As discussed in the above paragraph, it is obvious that Equation 6 expresses the region of expands (shrinks) until when i.e.,
By choosing the form of the function asbecause and Therefore, the last term of Equation 8, which is newly added, expresses the constraint of the constant volume of u since it has a minimum at
As shown in Figure 2, the region of takes the form of a circle in two dimensions and a sphere in three dimensions in the steady state. Thus, the shape of the cell in the simplest case can be described by a single-order parameter such that in the region with the cell ( in the region not taken up by the cell) with a constant Based on the fact that has an interface with a thickness on the order of the cell cortex can also be expressed as a function of u, e.g., (see Figure 2C).
In order to describe the multicellular system, a vector variable is considered, where is the total number of cells in the system. The component describes the shape of the m-th cell. We also use the variable to represent the shape of substances interacting with the cells, such as the wall, the substrate, and the extracellular matrix.
The model free energy for the multicellular system is written asdetermines the shape of the cell, describes the interactions between each cell, and expresses the interactions between the cells and substances external to them. The form of is obtained by modifying Equation 8 using the vector variable as follows: is the cell type of the m-th cell. The coefficients and are positive constants, where L is the total number of cell types in the system. As discussed previously, Equation 10 indicates that the thickness of the cell interface is on the order of and that the speed at which the volumes of the type- cells approach the target volume is controlled by the value of . That means determines the cell size growth. Here, can be presented in the following form: and are positive constants. The first term on the right-hand side of Equation 11 represents the effect of the excluded volume by increasing the energy if the cells overlap, whereas the second term represents the effect of cell adhesion by decreasing the energy if the cell cortices overlap. This adhesion term becomes negative in the region in which cell adhesion occurs. In order to prevent divergence due to this adhesion term, we introduce the third term on the right-hand side of Equation 11 with the condition whereby Similarly, the interaction between cells and substances external to the cells is expressed as follows: and are positive constants.
Taking the functional derivative of Equation 9 with respect to the following time evolution equations are obtained:is a positive constant, and is the Kronecker delta, which is if The vector variable is an auxiliary variable that is defined as follows: Figure 3, the region occupied by the type- cells can be identified by
Note that the interaction terms in Equation 13 are not written explicitly in terms of the variables but are instead written in terms of the auxiliary variable As discussed in Methods, the introducing is very useful for the simulation of a system having a large number of cells. The components and can also be presented in terms of as follows:
We adopted the second term on the right-hand side of Equation 14 and the first term on the right-hand side of Equation 15 to express the excluded volumes and the cell adhesions, respectively, because these terms are the simplest among the several alternatives, which can be written in terms of both in the time evolution equation for and the component .
Figure 4 shows the result of cell divisions in two dimensions. It is well known that the spindle positioning plays an important role in the stage of deciding the plane of cell division –. However, we consider here the simplest rule for cell division as the first step. The rule imposed here is that when the volume of the m-th cell become larger than where the m-the cell divides into two cells, and asand is a positive constant. The angle is taken randomly. Using this rule, the number of cells increase in time. Starting with the data in which a circular cell is located at the center of the number of cells become at For simplicity, the number of cell type is one, and the cell adhesion is not considered, It is noted that the scale of time can be determined by comparison with the experimental data of the cell cycle.
Figure 5 shows the numerical results for two cells of the same type, i.e., and with different adhesion strengths. The curves in the top row of the graphs indicate the contour lines of ( and 2), and the symbols indicate the positions of the centers of the cells The variable is given as follows:
The integral over r of is identical to the second term on the right-hand side of Equation 11. The and profiles along the dotted line in the top row have been plotted in the middle and bottom rows of the graphs, respectively. Since has a non-zero value only in regions in which cell adherence occurs, is an indicator of locations at which cell adherence occurs. Initially, the distance between the centers of cells is set to 1.400. After a sufficiently long simulation time the two cells move closer to each other as the value of increases, such that the distances between the cell centers are 1.574 in the case of Panel A with 1.280 in the case of Panel B with and 1.107 in the case of Panel C with
Figure 6 shows snapshots of three-dimensional simulations at The solid substrate is introduced by setting the variable s as where and are positive constants. The light gray surfaces are contour plots of and the dark gray surfaces represent contour plots of We set as 0.0000, 0.0100, and 0.0219 for the simulations shown in Panels A, B, and C, respectively, where the other parameters are the same for all cases. If the cell adhesions are weak, the cells push against each other, and their positions are determined as shown in Panel A. On the other hand, for the case in which the cell adhesions are sufficiently strong, the cell positions are decided by the pulling force between cells, and the surface of the cell layer becomes flat, as shown in Panel C.
Figure 7 shows the numerical results for cell deformation and rearrangement. A cell cluster of and is sandwiched between two walls that move at a constant speed. In this calculation, considering the variable s as an order parameter that corresponds to the walls, the time evolution of s is calculated as where is a positive constant. The locations of the left and right walls are denoted as and respectively. Panel A shows the results for the case in which the adhesion strength between cells of the same type is stronger than that between cells of different types ( and ), whereas Panel B shows the results for the opposite case and Light gray, dark gray, and black areas represent the positions of the type-1 cells, the type-2 cells, and the walls, respectively. Cells adhering to the walls are stretched by the moving walls, causing the cells to be deformed and rearranged. Cells that are rearranged as weakly adhered cells detach first. In Panel A, the cells detach from the left wall at approximately and relax to almost their original shape at The time evolution of the total energy E is plotted in Figure 8. The solid line shows the results for Panel A of Figure 7, and the dotted line shows the results for Panel B of Figure 7. There is no monotonic decrease in total energy because the walls stretch the cell clusters. Comparison of Figures 7 and 8 reveals that the energy decreases significantly when cell rearrangement occurs.
Finally, we show that the cell movements such as the chemotactic movement and the random movement can also be incorporated into the proposed model. The chemotactic movement of the cell can be described by adding a new term, such as to the right-hand side of Equation 13, where the variable is the chemical concentration in extracellular regions. The parameter indicates the sensitivity of the m-th cell to the gradient of c. Figure 9 shows the time evolution of a system with cells having chemotaxis. Light gray and dark gray represent type-1 and type-2 cells, respectively. In this case, we consider the variable s as an order parameter that corresponds to the wall. The fifty cells are surrounded by the unmoving wall defined as where and are positive constants. By setting and it is assumed that the only type-2 cells can sense the gradient of the chemical concentration c. For simplicity, cell adhesion is not considered and the form of c is assumed not to be affected by or t and is taken as where is a constant. It is found numerically that type-2 cells move toward the c-rich region by pressing against type-1 cells.
The random movement of cells can also be incorporated into the proposed model by adding a new term, such as to the right-hand side of Equation 13. The function indicates an uniform random number from to where is a positive constant. Figure 10 shows the result of cell sorting which has been known to require both of the random movement of cells and the cell adhesion , , . We obtained that differential adhesion with fluctuation leads the sorting of a mixture of two types of cells as reported in Ref. .
We proposed a new type of cell model based on a phase field model, including the effects of excluded volumes and cell adhesions. To our knowledge, this is the first study to apply the phase field model to multicellular systems. We succeeded to make a skillful method for reduction of the computational memory and simulation time using the auxiliary variable as discussed in Methods.
The proposed model is based on a concept similar to the cellular Potts model, but the time evolutions of cell shapes in the proposed model differ from those in the cellular Potts model. In the cellular Potts model, the time evolutions of the spins are computed by the Monte Carlo method, and thus the fluctuations are required for the time evolution. On the other hand, the time evolution equations in the present model are written in the form of partial differential equations, whereby fluctuations are not necessary in order to run the simulations. In addition, the proposed model is thought to be more appropriate for investigating problems in which a small volume variant must be accounted for, because the proposed model is continuous in any parameter.
Since the cell shapes are represented by interfaces of finite thickness, the proposed model has the potential to be applied to the investigation of not only shape changes due to interactions between cells (Figures 5 and 6) and rearrangements of cells in clusters (Figure 7) but also phenomena requiring knowledge of the position of the cell membrane and/or cortex. It is easy to incorporate additional cell behaviors such as chemotaxis (Figure 9) and random movement (Figure 10) into the proposed model by adding corresponding terms.
The proposed model can express the time evolution of changes in cell shape due to the interactions between cells, cell differentiation by changing the cell type, cell size growth, cell movement, and cell death by deleting the corresponding component of Thus, this model may well provide a useful tool for approaching the problem of morphogenesis, although this remains a subject for future study in order to estimate the parameters as well as the time scale by comparison with earlier models and with experimental data. Considering both of the adhesion and the random movement of cells, we will investigate the chemotactic movement by using the proposed model and compare the obtained results to those reported in Ref.  as the next step. We also plan to include the cell division, in the process of which the cortex of the dividing cell is known to be important as well as the spindle positioning –, in the present model and to approach the problem of morphogenesis.
In order to rapidly simulate a system having numerous cells, it is important to design a program that does not consume a large amount of computational memory and to increase the simulation speed. These two requirements are easily satisfied because Equation 13 is not written explicitly in terms of Once is obtained for each time step, the time evolution of can be computed independent of Such a program is fully compatible with parallel computation. Moreover, the shape of the m-th cell can be obtained by computing the equation for within the small region which covers the region of This reduces the computational memory and increases the simulation speed. The position which indicates the center position of measured for the entire system, must be moved along with the movement of the center position of the m-th cell. Since is realized outside the region the Dirichlet boundary condition must always be set for the small region In this paper, the periodic boundary conditions are imposed on the boundary of throughout the simulations.
The estimation of the required memory is described below. Since the number of cell types is generally much smaller than the number of cells the memory increase by introducing becomes smaller than the memory decrease by computing within the small region For simplicity, we assume that each of the cells has the same volume, i.e., and that the entire system is covered by the cells, i.e., Then, the computational memories for and are roughly estimated as and respectively, where is the spatial dimension and is the size of the spatial grid. Therefore, the total memory required to compute Equation 13 using is linearly dependent on On the other hand, in order to compute cell-cell interactions without using the value of must be preserved over the entire region Then, the computational memories for solving Equation 13 increase by These estimations reveal that the introduction of is very useful for computation in the case of a system that contains a large number of cells, even in three dimensions.
In fact, we have checked the required memory with and without adopting auxiliary variable by changing the maximum number of cells, All other settings are the same for Figure 4. We used MacPro (3.2 GHz Quad-Core Intel Xeon, 32 GB 800 MHz DDR2 FB-DIMM) for this purpose. If the auxiliary variable is not considered, Equation 13 should be solved in the whole region In this case, a segmentation fault occurs at start of simulation when is set to be larger than As discussed above, if the auxiliary variable is considered, the shape of the m-th cell can be obtained by computing the equation for within the small region In the case of the maximum number of cells can be set to be at a maximum without a segmentation fault. These results support our claim which is that the introducing the auxiliary variable is very useful for computation in the case of a system with numerous cells.
Competing Interests: The author has declared that no competing interests exist.
Funding: This work was supported by the Japan Science and Technology Agency, PRESTO. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
The author would like to thank M. Akiyama, H. Kitahata, R. Kobayashi, T. Sakurai, T. Shibata, and A. Tero for the valuable discussions.
|1.||Honda H,Tanemura M,Nagai T. Year: 2004A three-dimensional vertex dynamics cell model of space-filling polyhedra simulating cell behavior in a cell aggregate.J Theor Biol2264395314759650|
|2.||Nagai T,Honda H. Year: 2001A dynamic cell model for the formation of epithelial tissues.Philosophical Magazine B: Physics of Condensed Matter; Statistical Mechanics, Electronic, Optical and Magnetic Properties81699719|
|3.||Honda H. Year: 1978Description of cellular patterns by dirichlet domains: the two-dimensional case.J Theor Biol7252343672241|
|4.||Honda H,Yamanaka H,Dan-Sohkawa M. Year: 1984A computer simulation of geometrical configurations during cell division.J Theor Biol106423356717036|
|5.||Glazier JA,Graner F. Year: 1993Simulation of the differential adhesion driven rearrangement of biological cells.Phys Rev E4721282154|
|6.||Graner F,Glazier JA. Year: 1992Simulation of biological cell sorting using a two-dimensional extended potts model.Phys Rev Lett692013201610046374|
|7.||Weliky M,Minsuk S,Keller R,Oster G. Year: 1991Notochord morphogenesis in xenopus laevis: simulation of cell behavior underlying tissue convergence and extension.Development1131231441811939|
|8.||Graner F,Sawada Y. Year: 1993Can surface adhesion drive cell rearrangement? part ii: A geometrical model.J Theor Biol164477506|
|9.||Honda H,Morita T,Tanabe A. Year: 1979Establishment of epidermal cell columns in mammalian skin: computer simulation.J Theor Biol8174559537395|
|10.||Morishita Y,Iwasa Y. Year: 2008Growth based morphogenesis of vertebrate limb bud.Bull Math Biol7019577818668295|
|11.||Newman TJ. Year: 2007Single-Cell-Based Models in Biology and Medicine.Birkhauser, 221–239 pp|
|12.||Kafer J,Hogeweg P,Maree AF. Year: 2006Moving forward moving backward: directional sorting of chemotactic cells due to size and adhesion differences.PLoS Comput Biol2e5616789822|
|13.||Poplawski NJ,Shirinifard A,Swat M,Glazier JA. Year: 2008Simulation of single-species bacterial-biofilm growth using the gglazier-graner-hogeweg model and the compucell3d modeling environment.Mathematical Biosciences and Engineering535538818613738|
|14.||Folch R,Casademunt J,Hernandez-Machado A,Ramirez-Piscina L. Year: 1999Phase-field model for hele-shaw ows with arbitrary viscosity contrast. i. theoretical approach.Phys Rev E601724|
|15.||Karma A,Rappel WJ. Year: 1998Quantitative phase-field modeling of dendritic growth in two and three dimensions.Phys Rev E574323|
|16.||Karma A,Kessler D,Levine H. Year: 2001Phase-field model of mode iii dynamic fracture.Phys Rev Lett8704550111461627|
|17.||Kobayashi R. Year: 1993Modeling and numerical simulations of dendritic crystal growth.Physica D: Nonlinear Phenomena63410423|
|18.||Kockelkoren J,Levine H,Rappel WJ. Year: 2003Computational approach for modeling intra- and extracellular dynamics.Phys Rev E68037702|
|19.||Shao D,Rappel WJ,Levine H. Year: 2010Computational model for cell morphodynamics.Phys Rev Lett10510810420867552|
|20.||Akiyama M,Tero A,Kobayashi R. Year: 2010A mathematical model of cleavage.J Theor Biol264849420045703|
|21.||Grill SW,Howard J,Schaffer E,Stelzer EH,Hyman AA. Year: 2003The distribution of active force generators controls mitotic spindle position.Science3015182112881570|
|22.||Thery M,Jimenez-Dalmaroni A,Racine V,Bornens M,Julicher F. Year: 2007Experimental and theoretical study of mitotic spindle orientation.Nature447493617495931|
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