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. 2008 Dec 18;105(52):20834–20839. doi: 10.1073/pnas.0808700106

Fig. 4.

Fig. 4.

CD8αα T cell populations in the IEL. (A) The IEL from Rag KO recipients of DKO splenocytes, DKO splenocytes plus WT CD4 T cells (WT CD4), and DKO splenocytes plus VDR KO CD4 T cells (VDR KO CD4) cells (same mice as in Fig. 2B) were isolated and stained for CD4, CD8α, and CD8β. *, values in the WT CD4 group were significantly different from those in the VDR KO CD4 and DKO group, P < 0.05. **, values in the DKO only group were significantly different from those in the WT or VDR KO group, P < 0.05. (B) IEL were isolated from 6–8 VDR KO and WT mice and stained for CD4, CD8α, CD8β, and TCRβ. *, values in the WT group were significantly different from those in the VDR KO group, P < 0.01. Fig. S2 shows the isotype controls for staining and representative histograms.