Figure 7
Figure 7. CD137L regulates gene expression in GC B cells. CD19+GL7+ GC B cells were sorted by flow cytometry from spleen and lymph nodes of WT and CD137L−/− mice 9 days after immunization with NP-CG (left panel, GC1) or infection with influenza virus (middle panel, GC2). GC B cells of 4 mice per genotype were pooled for each experiment. mRNA was isolated and used for comparative expression analysis by genome-wide microarray. The heat map depicts transcript levels according to the indicated 2log ratio between expression in WT vs CD137−/− GC B cells (see color scale). Green denotes lower expression, and red denotes greater expression in WT GC B cells compared with CD137−/− GC B cells. The list of genes was selected for statistically significant differential expression (P < .01) and presence in both experiments. CD19+GL7− non-GC B cells (right panel, nonGC) were sorted simultaneously and analyzed to confirm GC specificity of the listed genes.

CD137L regulates gene expression in GC B cells. CD19+GL7+ GC B cells were sorted by flow cytometry from spleen and lymph nodes of WT and CD137L−/− mice 9 days after immunization with NP-CG (left panel, GC1) or infection with influenza virus (middle panel, GC2). GC B cells of 4 mice per genotype were pooled for each experiment. mRNA was isolated and used for comparative expression analysis by genome-wide microarray. The heat map depicts transcript levels according to the indicated 2log ratio between expression in WT vs CD137−/− GC B cells (see color scale). Green denotes lower expression, and red denotes greater expression in WT GC B cells compared with CD137−/− GC B cells. The list of genes was selected for statistically significant differential expression (P < .01) and presence in both experiments. CD19+GL7 non-GC B cells (right panel, nonGC) were sorted simultaneously and analyzed to confirm GC specificity of the listed genes.

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