The tipping points in the initiation of B cell signalling: how small changes make big differences

被引:137
作者
Pierce, Susan K. [1 ]
Liu, Wanli [1 ]
机构
[1] NIAID, NIH, Rockville, MD 20852 USA
基金
美国国家卫生研究院;
关键词
RESONANCE ENERGY-TRANSFER; RECEPTOR TYROSINE KINASES; SINGLE-MOLECULE TRACKING; BASOPHIL LEUKEMIA-CELLS; RESPONSES IN-VIVO; ANTIGEN RECEPTOR; PLASMA-MEMBRANE; SYNAPSE FORMATION; LIPID RAFTS; LYMPH-NODE;
D O I
10.1038/nri2853
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
B cells are selected by the binding of antigen to clonally distributed B cell receptors (BCRs), triggering signalling cascades that result in B cell activation. With the recent application of high-resolution live-cell imaging, we are gaining an understanding of the events that initiate BCR signalling within seconds of its engagement with antigen. These observations are providing a molecular explanation for fundamental aspects of B cell responses, including antigen affinity discrimination and the value of class switching, as well as insights into the underlying causes of B cell tumorigenesis. Advances in our understanding of the earliest molecular events that follow antigen binding to the BCR may provide a general framework for the initiation of signalling in the adaptive immune system.
引用
收藏
页码:767 / 777
页数:11
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