Fig. 7

B APN KO BMSCs were placed in the bottom chamber, splenocytes from EL-4-bearing WT mice were placed in the upper chamber of the transwell plate, and the population of migrated CD8+ T cells in the bottom chamber was analyzed by flow cytometry. C Cell lysates from the BMSCs were used to measure the levels of various chemokines. All dots were quantified using ImageJ software, and bar graphs were used for quantitative data