The Eph-related tyrosine kinase ligand Ephrin-B1 marks germinal center and memory precursor B cells

被引:95
作者
Laidlaw, Brian J. [1 ,2 ]
Schmidt, Timothy H. [1 ,2 ]
Green, Jesse A. [1 ,2 ]
Allen, Christopher D. C. [1 ,3 ,4 ]
Okada, Takaharu [5 ]
Cyster, Jason G. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Cardiovasc Res Inst, Dept Anat, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Sandler Asthma Basic Res Ctr, San Francisco, CA 94143 USA
[5] Ctr Integrat Med Sci IMS RCAI, Inst Phys & Chem Res, Lab Tissue Dynam, Yokohama, Kanagawa 2300045, Japan
基金
美国国家卫生研究院;
关键词
T-CELL; CENTER SELECTION; AID EXPRESSION; DIFFERENTIATION; GENE; ACTIVATION; MATURATION; RETENTION; SUBSETS; ANTIGEN;
D O I
10.1084/jem.20161461
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Identification of germinal center (GC) B cells is typically reliant on the use of surface activation markers that exhibit a wide range of expression. Here, we identify Ephrin-B1, a ligand for Eph-related receptor tyrosine kinases, as a specific marker of mature GC B cells. The number of Ephrin-B1(+) GC B cells increases during the course of an immune response with Ephrin-B1(+) GC B cells displaying elevated levels of Bcl6, S1pr2, and Aicda relative to their Ephrin-B1-counterparts. We further identified a small proportion of recently dividing, somatically mutated Ephrin-B1(+) GC B cells that have begun to down-regulate Bcl6 and S1pr2 and express markers associated with memory B cells, such as CD38 and EBI2. Transcriptional analysis indicates that these cells are developmentally related to memory B cells, and likely represent a population of GC memory precursor (PreMem) B cells. GC PreMem cells display enhanced survival relative to bulk GC B cells, localize near the edge of the GC, and are predominantly found within the light zone. These findings offer insight into the significant heterogeneity that exists within the GC B cell population and provide tools to further dissect signals regulating the differentiation of GC B cells.
引用
收藏
页码:639 / 649
页数:11
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