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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.

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