Multiple steady states and the form of response functions to antigen in a model for the initiation of T-cell activation

The aim of this paper is to study the qualitative behaviour predicted by a mathematical model for the initial stage of T-cell activation. The state variables in the model are the concentrations of phosphorylation states of the T-cell receptor (TCR) complex and the phosphatase SHP-1 in the cell. It i...

Full description

Bibliographic Details
Main Authors: Alan D. Rendall, Eduardo D. Sontag
Format: Article
Language:English
Published: The Royal Society 2017-01-01
Series:Royal Society Open Science
Subjects:
Online Access:https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.170821
id doaj-d234c26c8ca74523b2827292be5f8ea5
record_format Article
spelling doaj-d234c26c8ca74523b2827292be5f8ea52020-11-25T03:41:24ZengThe Royal SocietyRoyal Society Open Science2054-57032017-01-0141110.1098/rsos.170821170821Multiple steady states and the form of response functions to antigen in a model for the initiation of T-cell activationAlan D. RendallEduardo D. SontagThe aim of this paper is to study the qualitative behaviour predicted by a mathematical model for the initial stage of T-cell activation. The state variables in the model are the concentrations of phosphorylation states of the T-cell receptor (TCR) complex and the phosphatase SHP-1 in the cell. It is shown that these quantities cannot approach zero and that the model possesses more than one positive steady state for certain values of the parameters. It can also exhibit damped oscillations. It is proved that the chemical concentration which represents the degree of activation of the cell, that of the maximally phosphorylated form of the TCR complex, is, in general, a non-monotone function of the activating signal. In particular, there are cases where there is a value of the dissociation constant of the ligand from the receptor which produces a maximal activation of the T cell. This suggests that mechanisms taking place in the first few minutes after activation and included in the model studied in this paper suffice to explain the optimal dissociation time seen in experiments. In this way, the results of certain simulations in the literature have been confirmed rigorously and some important features which had not previously been seen have been discovered.https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.170821immunologyt cellsmultistationarity
collection DOAJ
language English
format Article
sources DOAJ
author Alan D. Rendall
Eduardo D. Sontag
spellingShingle Alan D. Rendall
Eduardo D. Sontag
Multiple steady states and the form of response functions to antigen in a model for the initiation of T-cell activation
Royal Society Open Science
immunology
t cells
multistationarity
author_facet Alan D. Rendall
Eduardo D. Sontag
author_sort Alan D. Rendall
title Multiple steady states and the form of response functions to antigen in a model for the initiation of T-cell activation
title_short Multiple steady states and the form of response functions to antigen in a model for the initiation of T-cell activation
title_full Multiple steady states and the form of response functions to antigen in a model for the initiation of T-cell activation
title_fullStr Multiple steady states and the form of response functions to antigen in a model for the initiation of T-cell activation
title_full_unstemmed Multiple steady states and the form of response functions to antigen in a model for the initiation of T-cell activation
title_sort multiple steady states and the form of response functions to antigen in a model for the initiation of t-cell activation
publisher The Royal Society
series Royal Society Open Science
issn 2054-5703
publishDate 2017-01-01
description The aim of this paper is to study the qualitative behaviour predicted by a mathematical model for the initial stage of T-cell activation. The state variables in the model are the concentrations of phosphorylation states of the T-cell receptor (TCR) complex and the phosphatase SHP-1 in the cell. It is shown that these quantities cannot approach zero and that the model possesses more than one positive steady state for certain values of the parameters. It can also exhibit damped oscillations. It is proved that the chemical concentration which represents the degree of activation of the cell, that of the maximally phosphorylated form of the TCR complex, is, in general, a non-monotone function of the activating signal. In particular, there are cases where there is a value of the dissociation constant of the ligand from the receptor which produces a maximal activation of the T cell. This suggests that mechanisms taking place in the first few minutes after activation and included in the model studied in this paper suffice to explain the optimal dissociation time seen in experiments. In this way, the results of certain simulations in the literature have been confirmed rigorously and some important features which had not previously been seen have been discovered.
topic immunology
t cells
multistationarity
url https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.170821
work_keys_str_mv AT alandrendall multiplesteadystatesandtheformofresponsefunctionstoantigeninamodelfortheinitiationoftcellactivation
AT eduardodsontag multiplesteadystatesandtheformofresponsefunctionstoantigeninamodelfortheinitiationoftcellactivation
_version_ 1724529892774641664