Figure 4
Figure 4. Ihh regulates thymus homeostasis. (A) Scatter plots show the percentage of cells in S + G2/M, measured by PI staining of FACS-sorted E16.5 CD25+ DN (left plot), CD8ISP (middle plot), and DP (right plot) populations from WT and Ihh+/− littermates, relative to the mean percentage in WT littermate populations. Differences in mean percentage between +/− and WT were statistically significant for CD25+ DN (P = .042) and CD8ISP (P = .040) populations, but not for DP cells (P = .981). (B) Scatter plots show relative thymocyte number from Ihh+/+Rag1−/− and Ihh+/−Rag1−/− thymi (relative to mean of Ihh+/+Rag1−/− littermates). Differences are significant by Student t test (P < .001). Mean thymocyte number: litter 1 Ihh+/+Rag1−/− 1.65 × 106, Ihh+/−Rag1−/− 1.33 × 106; litter 2 Ihh+/+Rag1−/− 1.7 × 106, Ihh+/−Rag1−/− 1.25 × 106; litter 3 Ihh+/+Rag1−/− 1.75 × 106, Ihh+/−Rag1−/− 1.31 × 106. (C) Bar chart shows fold increase in thymocyte number on induction of differentiation by treatment with 1 μg/mL anti-CD3 after 5 days of FTOCs for Rag1−/−Ihh+/+ and Rag1−/− Ihh+/− littermates. For each thymus, one lobe was cultured with anti-CD3 and the fold increase in cell number was calculated relative to the number of cells in the other untreated lobe. The fold increase in the Rag1−/−Ihh+/− was significantly different from that in the Rag1−/−Ihh+/+ by Student t test (P = .03). Mean thymocyte number: litter 1 Ihh+/+Rag1−/− untreated 1.65 × 106, Ihh+/+Rag1−/− + anti-CD3 1.425 × 107, Ihh+/−Rag1−/− untreated 1.33 × 106, Ihh+/−Rag1−/− + anti-CD3 1.725 × 107. Litter 2 Ihh+/+Rag1−/− untreated 1.7 × 106, Ihh+/+Rag1−/− + anti-CD3 1.49 × 107, Ihh+/−Rag1−/− untreated 1.245 × 106, Ihh+/+Rag1−/− + anti-CD3 1.689 × 107. (D) Dot plots show E17.5 WT, Ihh+/−, and Ihh−/− thymi stained with anti-CD4 and anti-CD8. Mean thymocyte number: litter 1 WT 2.05 × 106, Ihh+/− 3.3 × 106, Ihh−/− 2 × 106; litter 2 WT 3.5 × 106, Ihh+/− 2.865 × 106, Ihh−/− 8.5 × 105; litter 3 WT 3.35 × 106, Ihh+/− 2.63 × 106 Ihh−/− 1.675 × 106; litter 4 WT 3.35 × 106, Ihh+/− 2.336 × 106; litter 5 WT 3.868 × 106, Ihh+/− 3.69 × 106; litter 6 WT 4.8 × 106, Ihh+/− 4.756, Ihh−/− 3.8 × 106. (E) Scatter plot shows cell numbers (relative to mean of WT) from thymi from E17.5 WT, Ihh+/−, and Ihh−/− embryos. The difference in mean between WT and Ihh−/− is significant (P = .002, Student t test), and the difference in SD between WT and Ihh+/− is also significant (P < .001, F test). (F) Scatter plot shows : thymocyte number (relative to mean of WT) from E17.5 WT littermate and Ihh+/− embryos. Ihh+/− thymi are grouped by relative size into 3 sets: I, more than 1.3; II, 0.9 to 1.1; and III, less than 0.9; ○: the percentage of cells in S + G2/M (relative to mean of WT), measured by PI staining of FACS-sorted E17.5 CD25+ from WT and Ihh+/− mice grouped into 3 groups I, II, and III as detailed in this figure legend.

Ihh regulates thymus homeostasis. (A) Scatter plots show the percentage of cells in S + G2/M, measured by PI staining of FACS-sorted E16.5 CD25+ DN (left plot), CD8ISP (middle plot), and DP (right plot) populations from WT and Ihh+/− littermates, relative to the mean percentage in WT littermate populations. Differences in mean percentage between +/− and WT were statistically significant for CD25+ DN (P = .042) and CD8ISP (P = .040) populations, but not for DP cells (P = .981). (B) Scatter plots show relative thymocyte number from Ihh+/+Rag1−/− and Ihh+/−Rag1−/− thymi (relative to mean of Ihh+/+Rag1−/− littermates). Differences are significant by Student t test (P < .001). Mean thymocyte number: litter 1 Ihh+/+Rag1−/− 1.65 × 106, Ihh+/−Rag1−/− 1.33 × 106; litter 2 Ihh+/+Rag1−/− 1.7 × 106, Ihh+/−Rag1−/− 1.25 × 106; litter 3 Ihh+/+Rag1−/− 1.75 × 106, Ihh+/−Rag1−/− 1.31 × 106. (C) Bar chart shows fold increase in thymocyte number on induction of differentiation by treatment with 1 μg/mL anti-CD3 after 5 days of FTOCs for Rag1−/−Ihh+/+ and Rag1−/− Ihh+/− littermates. For each thymus, one lobe was cultured with anti-CD3 and the fold increase in cell number was calculated relative to the number of cells in the other untreated lobe. The fold increase in the Rag1−/−Ihh+/− was significantly different from that in the Rag1−/−Ihh+/+ by Student t test (P = .03). Mean thymocyte number: litter 1 Ihh+/+Rag1−/− untreated 1.65 × 106, Ihh+/+Rag1−/− + anti-CD3 1.425 × 107, Ihh+/−Rag1−/− untreated 1.33 × 106, Ihh+/−Rag1−/− + anti-CD3 1.725 × 107. Litter 2 Ihh+/+Rag1−/− untreated 1.7 × 106, Ihh+/+Rag1−/− + anti-CD3 1.49 × 107, Ihh+/−Rag1−/− untreated 1.245 × 106, Ihh+/+Rag1−/− + anti-CD3 1.689 × 107. (D) Dot plots show E17.5 WT, Ihh+/−, and Ihh−/− thymi stained with anti-CD4 and anti-CD8. Mean thymocyte number: litter 1 WT 2.05 × 106, Ihh+/− 3.3 × 106, Ihh−/− 2 × 106; litter 2 WT 3.5 × 106, Ihh+/− 2.865 × 106, Ihh−/− 8.5 × 105; litter 3 WT 3.35 × 106, Ihh+/− 2.63 × 106 Ihh−/− 1.675 × 106; litter 4 WT 3.35 × 106, Ihh+/− 2.336 × 106; litter 5 WT 3.868 × 106, Ihh+/− 3.69 × 106; litter 6 WT 4.8 × 106, Ihh+/− 4.756, Ihh−/− 3.8 × 106. (E) Scatter plot shows cell numbers (relative to mean of WT) from thymi from E17.5 WT, Ihh+/−, and Ihh−/− embryos. The difference in mean between WT and Ihh−/− is significant (P = .002, Student t test), and the difference in SD between WT and Ihh+/− is also significant (P < .001, F test). (F) Scatter plot shows : thymocyte number (relative to mean of WT) from E17.5 WT littermate and Ihh+/− embryos. Ihh+/− thymi are grouped by relative size into 3 sets: I, more than 1.3; II, 0.9 to 1.1; and III, less than 0.9; ○: the percentage of cells in S + G2/M (relative to mean of WT), measured by PI staining of FACS-sorted E17.5 CD25+ from WT and Ihh+/− mice grouped into 3 groups I, II, and III as detailed in this figure legend.

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