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. 2009 Dec 29;4(12):e8485. doi: 10.1371/journal.pone.0008485

Figure 5. Immunophenotypic and functional dissection of CX3CR1+ GC B cells.

Figure 5

(A) Double staining of CX3CR1+ GC B cells with CD27 and CD23 mAbs. Each B cell fraction was further characterized with mAbs (CD27+ cells, right lower panel; CD23+ cells, left lower panel). Results are median percent positive cells, maximum and minimum values from ten different experiments. (B) CX3CR1+ GC B cells were subjected to chemotaxis to 300 ng/ml rCX3CL1. Migrated cells were double stained for CD27 and CD23. One representative experiment out of seven is shown. (C) Purified GC B cells were subjected to CX3CL1-driven chemotaxis and migrated cells were collected and stained with a panel of mAbs. Results are median percent positive cells, maximum and minimum values from four different experiments.