Figure 2.
cGVHD induces T-cell infiltration and a proinflammatory cytokine profile in the brain. Messenger RNA expression of selected proinflammatory cytokines detected by quantitative real-time polymerase chain reaction in the thick coronal section (A) and hippocampus (B) of GVHD and TCD mice at days 35 and 70 after transplant (n = 6-15 mice per group; data pooled from 2 independent experiments). Expression calculated relative to the Hprt gene and reported as a fold change of the mean of the TCD group. (C) Schematic of transplantation regime. Lethally irradiated B6D2F1 recipient mice received 5 × 106 BM from C57Bl/6 donors ubiquitously expressing GFP and 0.5 × 106 sort-purified CD90.2+ T cells from C57Bl/6 donors ubiquitously expressing RFP. (D) Representative dot plots indicating gating strategy for identifying live CD90.2+ CD4 and CD8 T-cell subsets within the CD45hiCD11b− population, gated on forward and side scatter. Cells were isolated from digested coronal brain segments of transplant recipients at days 14, 35, and 70 after transplant. (E-I) Quantification of lymphocyte populations in dissociated GVHD brains at days 14, 35, and 70 after transplant. (E) CD90.2+ proportion of the CD45hiCD11b− population. (day 14: n = 6; data pooled from 2 independent experiments; day 35: n = 3; data from 1 independent experiment; day 70: n = 17; data pooled from 4 independent experiments). (F) Absolute number of CD90.2+ T cells within the CD45hiCD11b− population (day 14: n = 8; data pooled from 3 independent experiments; day 35: n = 6; data pooled from 2 independent experiments; day 70: n = 16; data pooled from 4 independent experiments). (G) Proportions of CD4+ and CD8+ T cells within the CD90.2+ population (day 14: n = 5; data pooled from 2 independent experiments; day 35: n = 7; data pooled from 2 independent experiments; day 70: n = 16; data pooled from 4 independent experiments). (H) Comparison of the proportions of CD8+ T cells derived from the T-cell (red) and BM (green) grafts (days 14 and 35: n = 3 mice per time point; day 70: n = 7; data pooled from 3 independent experiments). (I) Comparison of the proportions of CD4+ T cells derived from the T-cell (red) and BM (green) grafts (days 14 and 35: n = 3 mice per time point; day 70: n = 7; data pooled from 3 independent experiments). Data are presented as mean ± standard error of the mean. Significant differences calculated using unpaired Student t test (A-B) or 1-way analysis of variance with Tukey multiple comparisons test (E-H). *P < .05, **P < .01, ***P < .001, ****P < .0001.

cGVHD induces T-cell infiltration and a proinflammatory cytokine profile in the brain. Messenger RNA expression of selected proinflammatory cytokines detected by quantitative real-time polymerase chain reaction in the thick coronal section (A) and hippocampus (B) of GVHD and TCD mice at days 35 and 70 after transplant (n = 6-15 mice per group; data pooled from 2 independent experiments). Expression calculated relative to the Hprt gene and reported as a fold change of the mean of the TCD group. (C) Schematic of transplantation regime. Lethally irradiated B6D2F1 recipient mice received 5 × 106 BM from C57Bl/6 donors ubiquitously expressing GFP and 0.5 × 106 sort-purified CD90.2+ T cells from C57Bl/6 donors ubiquitously expressing RFP. (D) Representative dot plots indicating gating strategy for identifying live CD90.2+ CD4 and CD8 T-cell subsets within the CD45hiCD11b population, gated on forward and side scatter. Cells were isolated from digested coronal brain segments of transplant recipients at days 14, 35, and 70 after transplant. (E-I) Quantification of lymphocyte populations in dissociated GVHD brains at days 14, 35, and 70 after transplant. (E) CD90.2+ proportion of the CD45hiCD11b population. (day 14: n = 6; data pooled from 2 independent experiments; day 35: n = 3; data from 1 independent experiment; day 70: n = 17; data pooled from 4 independent experiments). (F) Absolute number of CD90.2+ T cells within the CD45hiCD11b population (day 14: n = 8; data pooled from 3 independent experiments; day 35: n = 6; data pooled from 2 independent experiments; day 70: n = 16; data pooled from 4 independent experiments). (G) Proportions of CD4+ and CD8+ T cells within the CD90.2+ population (day 14: n = 5; data pooled from 2 independent experiments; day 35: n = 7; data pooled from 2 independent experiments; day 70: n = 16; data pooled from 4 independent experiments). (H) Comparison of the proportions of CD8+ T cells derived from the T-cell (red) and BM (green) grafts (days 14 and 35: n = 3 mice per time point; day 70: n = 7; data pooled from 3 independent experiments). (I) Comparison of the proportions of CD4+ T cells derived from the T-cell (red) and BM (green) grafts (days 14 and 35: n = 3 mice per time point; day 70: n = 7; data pooled from 3 independent experiments). Data are presented as mean ± standard error of the mean. Significant differences calculated using unpaired Student t test (A-B) or 1-way analysis of variance with Tukey multiple comparisons test (E-H). *P < .05, **P < .01, ***P < .001, ****P < .0001.

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