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We are analyzing https://link.springer.com/article/10.1007/s00285-025-02223-y.

Title:
Phenotype structuring in collective cell migration: a tutorial of mathematical models and methods | Journal of Mathematical Biology
Description:
Populations are heterogeneous, deviating in numerous ways. Phenotypic diversity refers to the range of traits or characteristics across a population, where for cells this could be the levels of signalling, movement and growth activity, etc. Clearly, the phenotypic distribution – and how this changes over time and space – could be a major determinant of population-level dynamics. For instance, across a cancerous population, variations in movement, growth, and ability to evade death may determine its growth trajectory and response to therapy. In this review, we discuss how classical partial differential equation (PDE) approaches for modelling cellular systems and collective cell migration can be extended to include phenotypic structuring. The resulting non-local models – which we refer to as phenotype-structured partial differential equations (PS-PDEs) – form a sophisticated class of models with rich dynamics. We set the scene through a brief history of structured population modelling, and then review the extension of several classic movement models – including the Fisher-KPP and Keller-Segel equations – into a PS-PDE form. We proceed with a tutorial-style section on derivation, analysis, and simulation techniques. First, we show a method to formally derive these models from underlying agent-based models. Second, we recount travelling waves in PDE models of spatial spread dynamics and concentration phenomena in non-local PDE models of evolutionary dynamics, and combine the two to deduce phenotypic structuring across travelling waves in PS-PDE models. Third, we discuss numerical methods to simulate PS-PDEs, illustrating with a simple scheme based on the method of lines and noting the finer points of consideration. We conclude with a discussion of future modelling and mathematical challenges.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
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Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

We can't tell how the site generates income.

While profit motivates many websites, others exist to inspire, entertain, or provide valuable resources. Websites have a variety of goals. And this might be one of them. Link.springer.com might have a hidden revenue stream, but it's not something we can detect.

Keywords {🔍}

google, scholar, models, rho, population, cell, model, mathematical, mathscinet, phenotypic, mathbb, left, endaligned, pspde, beginaligned, dynamics, journal, form, phenotype, partial, cells, varepsilon, populations, equiv, growth, quad, biology, pde, equation, lorenzi, time, spatial, travelling, displaystyle, equations, state, nonlocal, rightarrow, function, space, mathcal, solutions, analysis, modelling, movement, waves, varvecy, varvecx, proliferation, wave,

Topics {✒️}

$$\begin{aligned} \partial _t uk/ons/guide-method/census/2011/census-history/200-years $$\begin{aligned} n_{\varepsilon } $$\begin{aligned} \rho _\varepsilon time-dependent advection-diffusion-reaction equations rescaled taxis-based ps-pde model \partial ^2_{yy} partial ^2_{yy} }{\partial ^2_{yy} } \partial ^2_{yy} dipartimento di scienze $$\begin{aligned} \psi _x big ]}_{\begin{array}{ exp \left[ -\dfrac{\left displaystyle {\rho _\varepsilon basic reaction-advection-diffusion framework $$\begin{aligned} n_{ grant prin2022-pnrr project partial differential equations exp \left[ -\frac{\left }_{\begin{array}{ age-structured reaction-diffusion model partial differential equation monotonic upstream-centered scheme nonlocal lotka-volterra equations patlak-keller-segel chemotaxis model vector-host epidemic model lotka-volterra parabolic equations multiscale dti-based model equation $$\begin{aligned} $$\begin{aligned} a_y incorporate pressure-dependent inhibition reaction-advection-diffusion equation nonlocal reaction-diffusion equation nonlocal reaction-diffusion model hamilton-jacobi equation subject exploring ligand-receptor dynamics $$\begin{aligned} a_{ local reaction-diffusion equations adding sink/source terms age-structured models arising dfrac{h_x}{\tau } \left relation $$\begin{aligned} cell-cell recognition phenomenon relations $$\begin{aligned} rescaled fisher-kpp equation stochastic birth-death process reaching ps-pde models validate ps-pde models form $$\begin{aligned}

Questions {❓}

  • Can similar detail be absorbed within continuous models?
  • Discrete, continuous, or both?
  • How can we form a bridge, spanning discrete to continuous populations according to phenotypic state?
  • Surveys served purposes from economic (how much tax can we collect?
  • Theveneau E, Linker C (2017) Leaders in collective migration: are front cells really endowed with a particular set of skills?
  • A population continuously structured across some phenotypic space?

Schema {🗺️}

WebPage:
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         headline:Phenotype structuring in collective cell migration: a tutorial of mathematical models and methods
         description:Populations are heterogeneous, deviating in numerous ways. Phenotypic diversity refers to the range of traits or characteristics across a population, where for cells this could be the levels of signalling, movement and growth activity, etc. Clearly, the phenotypic distribution – and how this changes over time and space – could be a major determinant of population-level dynamics. For instance, across a cancerous population, variations in movement, growth, and ability to evade death may determine its growth trajectory and response to therapy. In this review, we discuss how classical partial differential equation (PDE) approaches for modelling cellular systems and collective cell migration can be extended to include phenotypic structuring. The resulting non-local models – which we refer to as phenotype-structured partial differential equations (PS-PDEs) – form a sophisticated class of models with rich dynamics. We set the scene through a brief history of structured population modelling, and then review the extension of several classic movement models – including the Fisher-KPP and Keller-Segel equations – into a PS-PDE form. We proceed with a tutorial-style section on derivation, analysis, and simulation techniques. First, we show a method to formally derive these models from underlying agent-based models. Second, we recount travelling waves in PDE models of spatial spread dynamics and concentration phenomena in non-local PDE models of evolutionary dynamics, and combine the two to deduce phenotypic structuring across travelling waves in PS-PDE models. Third, we discuss numerical methods to simulate PS-PDEs, illustrating with a simple scheme based on the method of lines and noting the finer points of consideration. We conclude with a discussion of future modelling and mathematical challenges.
         datePublished:2025-05-16T00:00:00Z
         dateModified:2025-05-16T00:00:00Z
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            Collective cell dynamics
            Cell movement
            Non-local PDEs
            Travelling waves
            Concentration phenomena
            35C07
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      headline:Phenotype structuring in collective cell migration: a tutorial of mathematical models and methods
      description:Populations are heterogeneous, deviating in numerous ways. Phenotypic diversity refers to the range of traits or characteristics across a population, where for cells this could be the levels of signalling, movement and growth activity, etc. Clearly, the phenotypic distribution – and how this changes over time and space – could be a major determinant of population-level dynamics. For instance, across a cancerous population, variations in movement, growth, and ability to evade death may determine its growth trajectory and response to therapy. In this review, we discuss how classical partial differential equation (PDE) approaches for modelling cellular systems and collective cell migration can be extended to include phenotypic structuring. The resulting non-local models – which we refer to as phenotype-structured partial differential equations (PS-PDEs) – form a sophisticated class of models with rich dynamics. We set the scene through a brief history of structured population modelling, and then review the extension of several classic movement models – including the Fisher-KPP and Keller-Segel equations – into a PS-PDE form. We proceed with a tutorial-style section on derivation, analysis, and simulation techniques. First, we show a method to formally derive these models from underlying agent-based models. Second, we recount travelling waves in PDE models of spatial spread dynamics and concentration phenomena in non-local PDE models of evolutionary dynamics, and combine the two to deduce phenotypic structuring across travelling waves in PS-PDE models. Third, we discuss numerical methods to simulate PS-PDEs, illustrating with a simple scheme based on the method of lines and noting the finer points of consideration. We conclude with a discussion of future modelling and mathematical challenges.
      datePublished:2025-05-16T00:00:00Z
      dateModified:2025-05-16T00:00:00Z
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         Phenotype-structured populations
         Collective cell dynamics
         Cell movement
         Non-local PDEs
         Travelling waves
         Concentration phenomena
         35C07
         35R09
         92B05
         92C17
         92D25
         Mathematical and Computational Biology
         Applications of Mathematics
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            address:
               name:Department of Mathematical Sciences “G. L. Lagrange”, Politecnico di Torino, Torino, Italy
               type:PostalAddress
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      name:Kevin J. Painter
      url:http://orcid.org/0000-0003-3273-6031
      affiliation:
            name:Politecnico di Torino
            address:
               name:Dipartimento Interateneo di Scienze, Progetto e Politiche del Territorio, Politecnico di Torino, Torino, Italy
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Chiara Villa
      affiliation:
            name:Sorbonne Université, CNRS, Université de Paris, Inria, Laboratoire Jacques-Louis Lions UMR 7598
            address:
               name:Sorbonne Université, CNRS, Université de Paris, Inria, Laboratoire Jacques-Louis Lions UMR 7598, Paris, France
               type:PostalAddress
            type:Organization
            name:Université Paris-Saclay, Inria, Centre Inria de Saclay
            address:
               name:Université Paris-Saclay, Inria, Centre Inria de Saclay, Palaiseau, France
               type:PostalAddress
            type:Organization
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      name:Department of Mathematical Sciences “G. L. Lagrange”, Politecnico di Torino, Torino, Italy
      name:Dipartimento Interateneo di Scienze, Progetto e Politiche del Territorio, Politecnico di Torino, Torino, Italy
      name:Sorbonne Université, CNRS, Université de Paris, Inria, Laboratoire Jacques-Louis Lions UMR 7598, Paris, France
      name:Université Paris-Saclay, Inria, Centre Inria de Saclay, Palaiseau, France

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