A Simple Framework for Agent-Based Modeling with Extracellular Matrix

被引:0
作者
Metzcar, John [1 ,2 ]
Duggan, Ben S. [3 ]
Fischer, Brandon [1 ]
Murphy, Matthew [2 ]
Heiland, Randy [1 ]
Macklin, Paul [1 ]
机构
[1] Indiana Univ, Intelligent Syst Engn, 700 N Woodlawn Ave, Bloomington, IN 47408 USA
[2] Indiana Univ, Informat, 901 E Tenth St, Bloomington, IN 47408 USA
[3] Indiana Univ, Comp Sci, 700 N Woodlawn Ave, Bloomington, IN 47408 USA
基金
美国国家科学基金会;
关键词
Extracellular matrix; Agent-based modeling; Collective migration; Stigmergy; Fibrosis; Cancer and basement membrane invasion; CELL-BASED MODEL; MATHEMATICAL-MODEL; STROMAL INTERACTIONS; MIGRATION; INVASION; POTTS; ALIGNMENT; DYNAMICS; REQUIRES; REPAIR;
D O I
10.1007/s11538-024-01408-8
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Extracellular matrix (ECM) is a key component of the cellular microenvironment and critical in multiple disease and developmental processes. Representing ECM and cell-ECM interactions is a challenging multiscale problem as they span molecular-level details to tissue-level dynamics. While several computational frameworks exist for ECM modeling, they often focus on very detailed modeling of individual ECM fibers or represent only a single aspect of the ECM. Using the PhysiCell agent-based modeling platform, we developed a framework of intermediate detail with the ability to capture bidirectional cell-ECM interactions. We represent a small region of ECM, an ECM element, with three variables describing its local microstructure: anisotropy, density, and overall fiber orientation. To spatially model the ECM, we use an array of ECM elements. Cells remodel local ECM microstructure and in turn, local microstructure impacts cellular motility. We demonstrate the utility of this framework and reusability of its core cell-ECM interaction model through examples in cellular invasion, wound healing, basement membrane degradation, and leader-follower collective migration. Despite the relative simplicity of the framework, it is able to capture a broad range of cell-ECM interactions of interest to the modeling community. Furthermore, variables representing the ECM microstructure are accessible through simple programming interfaces. This allows them to impact cell behaviors, such as proliferation and death, without requiring custom code for each interaction, particularly through PhysiCell's modeling grammar, enabling rapid modeling of a diverse range of cell-matrix biology. We make this framework available as a free and open source software package at https://github.com/PhysiCell-Models/collective-invasion.
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页数:32
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共 83 条
[61]  
Sherratt J.A., Chaplain M.A.J., A new mathematical model for avascular tumour growth, J Math Biol, 43, 4, pp. 291-312, (2001)
[62]  
Sherratt J.A., Dallon J.C., Theoretical models of wound healing: past successes and future challenges, CR Biol, 325, 5, pp. 557-564, (2002)
[63]  
Shuttleworth R., Trucu D., Multiscale modelling of fibres dynamics and cell adhesion within moving boundary cancer invasion, Bull Math Biol, 81, 7, pp. 2176-2219, (2019)
[64]  
Shuttleworth R., Trucu D., Cell-scale degradation of peritumoural extracellular matrix fibre network and its role within tissue-scale cancer invasion, Bull Math Biol, 82, 6, (2020)
[65]  
Stoll G., Caron B., Viara E., Dugourd A., Zinovyev A., Naldi A., Kroemer G., Barillot E., Calzone L., MaBoSS 2.0: an environment for stochastic Boolean modeling, Bioinformatics, 33, 14, pp. 2226-2228, (2017)
[66]  
Strell C., Paulsson J., Jin S.-B., Tobin N.P., Mezheyeuski A., Roswall P., Mutgan C., Mitsios N., Johansson H., Wickberg S.M., Svedlund J., Nilsson M., Hall P., Mulder J., Radisky D.C., Pietras K., Bergh J., Lendahl U., Warnberg F., Ostman A., Impact of epithelial-stromal interactions on peritumoral fibroblasts in ductal carcinoma in situ, JNCI: J Nat Cancer Inst, 111, 9, pp. 983-995, (2019)
[67]  
Suveges S., Chamseddine I., Rejniak K.A., Eftimie R., Trucu D., Collective Cell Migration in a Fibrous Environment: A Hybrid Multiscale Modelling Approach, Frontiers in Applied Mathematics and Statistics, 7, (2021)
[68]  
Szabo A., Varga K., Garay T., Hegedus B., Czirok A., Invasion from a cell aggregate–the roles of active cell motion and mechanical equilibrium, Phys Biol, 9, 1, (2012)
[69]  
Szabo P.M., Vajdi A., Kumar N., Tolstorukov M.Y., Chen B.J., Edwards R., Ligon K.L., Chasalow S.D., Chow K.-H., Shetty A., Bolisetty M., Holloway J.L., Golhar R., Kidd B.A., Hull P.A., Houser J., Vlach L., Siemers N.O., Saha S., Cancer-associated fibroblasts are the main contributors to epithelial-to-mesenchymal signatures in the tumor microenvironment, Sci Rep, 13, 1, (2023)
[70]  
Thrivikraman G., Jagiello A., Lai V.K., Johnson S.L., Keating M., Nelson A., Schultz B., Wang C.M., Levine A.J., Botvinick E.L., Tranquillo R.T., Cell contact guidance via sensing anisotropy of network mechanical resistance, Proc Natl Acad Sci, 118, 29, (2021)