On-Lattice Simulation of T Cell Motility, Chemotaxis, and Trafficking in the Lymph Node Paracortex

被引:23
作者
Bogle, Gib [1 ,3 ]
Dunbar, P. Rod [1 ,2 ]
机构
[1] Univ Auckland, Maurice Wilkins Ctr, Auckland, New Zealand
[2] Univ Auckland, Sch Biol Sci, Auckland, New Zealand
[3] Univ Auckland, Auckland Bioengn Inst, Auckland, New Zealand
来源
PLOS ONE | 2012年 / 7卷 / 09期
关键词
PRIMARY IMMUNE-RESPONSE; LYMPHOCYTES IN-VIVO; DENDRITIC CELLS; 2-PHOTON MICROSCOPY; MIGRATION; EGRESS; DYNAMICS; ANTIGEN; ACTIVATION; RECEPTOR;
D O I
10.1371/journal.pone.0045258
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Agent-based simulation is a powerful method for investigating the complex interplay of the processes occurring in a lymph node during an adaptive immune response. We have previously established an agent-based modeling framework for the interactions between T cells and dendritic cells within the paracortex of lymph nodes. This model simulates in three dimensions the "random-walk" T cell motility observed in vivo, so that cells interact in space and time as they process signals and commit to action such as proliferation. On-lattice treatment of cell motility allows large numbers of densely packed cells to be simulated, so that the low frequency of T cells capable of responding to a single antigen can be dealt with realistically. In this paper we build on this model by incorporating new numerical methods to address the crucial processes of T cell ingress and egress, and chemotaxis, within the lymph node. These methods enable simulation of the dramatic expansion and contraction of the T cell population in the lymph node paracortex during an immune response. They also provide a novel probabilistic method to simulate chemotaxis that will be generally useful in simulating other biological processes in which chemotaxis is an important feature.
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页数:13
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