Fig. 2: T cell development in ABab-I, ABab-A2, and C57BL6/N mice. | Nature Communications

Fig. 2: T cell development in ABab-I, ABab-A2, and C57BL6/N mice.

From: Mice with a diverse human T cell receptor repertoire selected on multiple HLA class I molecules

Fig. 2

A Representative flow cytometry analysis of thymocyte staining from ABab-I, ABab-A2, and C57BL6/N mice (n = 5). 1st lane: CD4+ and CD8+ single- and double-positive cells, gated on total thymocytes; 2nd lane: cell percentages of CD5+CD69+ cells, gated on lymphocytes; 3rd lane: percentages of CD3+ cells; 4th lane: CD4+ and CD8+ single- and double-positive cells gated on CD3+ cells. B Quantified cell numbers of thymocyte populations: CD8SP, DP, CD5CD69, and CD3CD8 in respective mouse strains. C Quantified percentages of thymocyte populations: CD8SP, DP, DN, and CD4SP in respective mouse strains. D Representative flow cytometry analysis of splenocyte staining from ABab-I, ABab-A2, and C57BL6/N mice (n = 5), gated on CD3+ lymphocytes. 1st lane: CD8+CD44high cells; 2nd lane: CD4+CD44high cells. E Quantified percentages of CD44high CD4+ and CD8+ populations from ABab-I, ABab-A2, and C57BL6/N mice (n = 5). Data in (B), (C), and (E) are presented as mean ± SD. Multiple group statistical comparisons were performed by one-way ANOVA, followed by pairwise comparisons using two-tailed unpaired Student’s t-test. P values indicate: *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001; ns not significant. Exact P values and source data are available in the Source Data file.

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