Figure 3
Figure 3. Role of miR-17-92 on donor T-cell migration and expression of chemokine receptor and integrin. BMT was carried out as outlined in Figure 2A, in which 1 × 106/mouse donor T cells were transplanted. Fourteen days post-BMT, recipient spleens and livers were collected and mononuclear cells were isolated and subjected to cell counting and FACS staining. Absolute numbers of donor H2Kb+Ly5.1–CD4+ or CD8+ WT (gray symbols) and KO (black symbols) T cells were shown in spleen (A) or liver (B). % CXCR3+ cells were shown on gated H2Kb+Ly5.1–CD4+ or CD8+ T cells in spleen (C-D). % α4β7+ cells were shown on gated H2Kb+Ly5.1–CD4+ or CD8+ T cells in spleen (E-F). Data shown were pooled from 2 replicated experiments (N = 10/group). *P < .05, **P < .01, ***P < .001.

Role of miR-17-92 on donor T-cell migration and expression of chemokine receptor and integrin. BMT was carried out as outlined in Figure 2A, in which 1 × 106/mouse donor T cells were transplanted. Fourteen days post-BMT, recipient spleens and livers were collected and mononuclear cells were isolated and subjected to cell counting and FACS staining. Absolute numbers of donor H2Kb+Ly5.1CD4+ or CD8+ WT (gray symbols) and KO (black symbols) T cells were shown in spleen (A) or liver (B). % CXCR3+ cells were shown on gated H2Kb+Ly5.1CD4+ or CD8+ T cells in spleen (C-D). % α4β7+ cells were shown on gated H2Kb+Ly5.1CD4+ or CD8+ T cells in spleen (E-F). Data shown were pooled from 2 replicated experiments (N = 10/group). *P < .05, **P < .01, ***P < .001.

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