<abstract xmlns="http://www.w3.org/1999/xhtml"><p> Biological systems are typically formed by different cell phenotypes, characterized by specific biological properties and behaviors. In particular, cells are able to undergo phenotypic transitions (i.e., activation or differentiation) upon internal or external stimuli. In order to take these phenomena into account, we here propose a modelling framework in which cell ensembles can be described collectively (i.e., through a distributed mass density) or individually (i.e., as a group of pointwise/concentrated particles) according to their biological determinants. A set of suitable rules involving the introduction of a cell shape function then defines a coherent procedure to model cell activation mechanisms, which imply a switch between the two mathematical representations. The theoretical environment describing cell transition is then enriched by including cell migratory dynamics and duplication/apoptotic processes, as well as the kinetics of selected diffusing chemicals inuencing the system evolution. Remarkably, our approach provides consistency of the same modeling framework across all types of cell representation, as it is suitable to cope with the often ambiguous translation of individual cell arguments (i.e., cell dimensions and interaction radii) into collective cell descriptions. Biologically relevant numerical realizations are also presented: in particular, they deal with phenotypic transitions within cell colonies and with the growth of a tumor spheroid. These phenomena constitute biological systems particularly suitable to assess the advantages of the proposed model and to analyze the role on cell dynamics both of relevant parameters and of the specific form given to the cell shape function. </p></abstract>

Biological systems are typically formed by different cell phenotypes, characterized by specific biological properties and behaviors. In particular, cells are able to undergo phenotypic transitions (i.e., activation or differentiation) upon internal or external stimuli. In order to take these phenomena into account, we here propose a modelling framework in which cell ensembles can be described collectively (i.e., through a distributed mass density) or individually (i.e., as a group of pointwise/concentrated particles) according to their biological determinants. A set of suitable rules involving the introduction of a cell shape function then defines a coherent procedure to model cell activation mechanisms, which imply a switch between the two mathematical representations. The theoretical environment describing cell transition is then enriched by including cell migratory dynamics and duplication/apoptotic processes, as well as the kinetics of selected diffusing chemicals inuencing the system evolution. Remarkably, our approach provides consistency of the same modeling framework across all types of cell representation, as it is suitable to cope with the often ambiguous translation of individual cell arguments (i.e., cell dimensions and interaction radii) into collective cell descriptions. Biologically relevant numerical realizations are also presented: in particular, they deal with phenotypic transitions within cell colonies and with the growth of a tumor spheroid. These phenomena constitute biological systems particularly suitable to assess the advantages of the proposed model and to analyze the role on cell dynamics both of relevant parameters and of the specific form given to the cell shape function.

A coherent modeling procedure to describe cell activation in biological systems

Communications in Applied and Industrial Mathematics

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

{"article-title":"A coherent modeling procedure to describe cell activation in biological systems"}

Biological systems are typically formed by different cell phenotypes, characterized by specific biological properties and behaviors. In particular, cells are...

A coherent modeling procedure to describe cell activation in biological systems

Publié en ligne: 22 mars 2017

Pages: 1 - 22

Reçu: 28 nov. 2016

Accepté: 16 févr. 2017

DOI: https://doi.org/10.1515/caim-2017-0001

Mots clés
multiscale modeling, hybrid systems, cell differentiation, cell phenotypic transition, multiscale dynamics

© 2017

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

A coherent modeling procedure to describe cell activation in biological systems

Publié en ligne: 22 mars 2017

Pages: 1 - 22

Reçu: 28 nov. 2016

Accepté: 16 févr. 2017

DOI: https://doi.org/10.1515/caim-2017-0001

Mots clésmultiscale modeling, hybrid systems, cell differentiation, cell phenotypic transition, multiscale dynamics

© 2017

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

Mots clés
multiscale modeling, hybrid systems, cell differentiation, cell phenotypic transition, multiscale dynamics