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. Author manuscript; available in PMC: 2011 Oct 29.
Published in final edited form as: Immunity. 2010 Sep 30;33(4):607–619. doi: 10.1016/j.immuni.2010.09.009

Figure 6. Expression of miR-155 by CD4+ T cells is required for proper development of inflammatory T cells during EAE.

Figure 6

A. 5×106 WT or Mir155−/− CD4+ T cells from naïve mice were injected i.v. into Rag1−/− recipients, EAE was induced with MOG35–55 24 hours later, and disease was scored over a time course (n=5–6). Data represent two independent experiments. B. Mice were harvested and engraftment of CD3+CD4+ T cells was assayed by flow cytometry using splenocytes (top). Expression of IL-17A and IFN-γ by CD4+ cells in the spleens and LNs was assayed by intracellular staining followed by flow cytometry. A representative plot from the LNs is shown (bottom). C. The averages of 5–6 mice per group are shown graphically. D. Mir155+/+ and Mir155−/− mice were injected with 1×107 WT CD45.1+CD4+ naïve T cells, and EAE was induced 24 hours later (n=5). Disease symptoms were scored over a time course. Data represent two independent experiments. E. Mice were harvested and CD4+ T cells in the brains were analyzed by flow cytometry to detect cells expressing CD45.1, IL-17A and IFN-γ. F. The average of 5 mice per group from (E.). Error bars represent +/−SEM and * denotes statistical significance with a p value of <0.05 according to a student’s two-tailed t-test. +/+ = Mir155+/+; −/− = Mir155−/−. See also Figure S4.