Guidance of B Cells by the Orphan G Protein-Coupled Receptor EBI2 Shapes Humoral Immune Responses

被引:227
作者
Gatto, Dominique [1 ]
Paus, Didrik [2 ]
Basten, Antony [1 ,3 ]
Mackay, Charles R. [1 ,3 ]
Brink, Robert [1 ,3 ]
机构
[1] Garvan Inst Med Res, Darlinghurst, NSW 2010, Australia
[2] Centenary Inst Canc Med & Cell Biol, Newtown, NSW 2042, Australia
[3] Univ New S Wales, St Vincents Clin Sch, Sydney, NSW 2010, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
PLASMA-CELL; SOMATIC HYPERMUTATION; DENDRITIC CELLS; ACTIVATION; MIGRATION; GENES; MICROENVIRONMENTS; DIFFERENTIATION; RESPONSIVENESS; ORGANIZATION;
D O I
10.1016/j.immuni.2009.06.016
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Humoral immunity depends on both rapid and long-term antibody production against invading pathogens. This is achieved by the generation of spatially distinct extrafollicular plasmablast and follicular germinal center (GC) B cell populations, but the signals that guide responding B cells to these alternative compartments have not been fully elucidated. Here, we show that expression of the orphan G protein-coupled receptor Epstein-Barr virus-induced gene 2 (EBI2, also known as GPR183) by activated B cells was essential for their movement to extrafollicular sites and induction of early plasmablast responses. Conversely, downregulation of EBI2 enabled B cells to access the center of follicles and promoted efficient GC formation. EBI2 therefore provides a previously uncharacterized dimension to B cell migration that is crucial for coordinating rapid versus long-term antibody responses.
引用
收藏
页码:259 / 269
页数:11
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