B cell antigen extraction is regulated by physical properties of antigen-presenting cells

被引:100
作者
Spillane, Katelyn M. [1 ,2 ]
Tolar, Pavel [1 ,2 ]
机构
[1] Francis Crick Inst, Immune Receptor Activat Lab, London NW1 1AT, England
[2] Imperial Coll London, Div Immunol & Inflammat, London SW7 2AZ, England
基金
英国医学研究理事会; 欧洲研究理事会; 英国惠康基金;
关键词
FOLLICULAR DENDRITIC CELLS; IMMUNE-COMPLEXES; GERMINAL CENTER; LYMPH-NODE; AFFINITY DISCRIMINATION; SUBCAPSULAR SINUS; ACTIVATION; SYNAPSE; LYSOSOMES; DYNAMICS;
D O I
10.1083/jcb.201607064
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Antibody production and affinity maturation are driven by B cell extraction and internalization of antigen from immune synapses. However, the extraction mechanism remains poorly understood. Here we develop DNA-based nano sensors to interrogate two previously proposed mechanisms, enzymatic liberation and mechanical force. Using antigens presented by either artificial substrates or live cells, we show that B cells primarily use force-dependent extraction and resort to enzymatic liberation only if mechanical forces fail to retrieve antigen. The use of mechanical forces renders antigen extraction sensitive to the physical properties of the presenting cells. We show that follicular dendritic cells are stiff cells that promote strong B cell pulling forces and stringent affinity discrimination. In contrast, dendritic cells are soft and promote acquisition of low-affinity antigens through low forces. Thus, the mechanical properties of B cell synapses regulate antigen extraction, suggesting that distinct properties of presenting cells support different stages of B cell responses.
引用
收藏
页码:217 / 230
页数:14
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