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. Author manuscript; available in PMC: 2011 Mar 27.
Published in final edited form as: Transplantation. 2010 Mar 27;89(6):667–676. doi: 10.1097/TP.0b013e3181ca9048

Figure 6. LPS promotes the survival of proliferating, HEL-CTL-treated MD-4 B cells.

Figure 6

MD-4 mice were bred onto the CD45.1 background, and CFSE-labeled splenocytes transferred into congenic C57BL/6 (CD45.1-CD45.2+) mice. HEL-CTL or vector-control CTL were transferred as in figure 5. LPS or saline (No LPS) was administered i.p. on the day of transfer. Lymphocytes in the spleen and LN were isolated 6 d later, and gated on the adoptively transferred CD45.1+ cells. (A) IgMa and CFSE staining among splenocytes. Numbers of dots on the different plots were normalized to show approximately equivalent numbers of IgMa- CFSE+ cells, which comprise primarily transferred T cells. Percent of IgMa- CFSE+ and IgMa+ cells are indicated in the respective boxes. (B) Analyses were performed as in (A), but for LN cells. Representative plots are shown.