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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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