Figure 2
Figure 2. Anti-CD3ε mAb treatment induces RAG2R229Q thymic expansion and DN to DP transition, without positive selection. RAG2R229Q mice were intraperitoneally injected at the 3rd and 13th day after birth with 25 μg of anti-CD3ε mAb or PBS and killed 2 months after last injection. (A top) Macroscopic aspect of a representative RAG2R229Q thymus from mice treated with PBS or anti-CD3ε mAb. (Bottom) Length and weight of thymi from the 2 groups (n = 5); **P = .0079. (B) Absolute number of thymic cells from RAG2R229Q mice injected with PBS (n = 17) and anti-CD3ε mAb (n = 20); ***P < .0001. (C left panel) Representative dot plots of thymocyte distribution from the indicated mice. (Right panel) Graph shows the frequency of DN, DP, CD4+TCRb+ SP, and CD8+TCRβ+ SP populations in PBS (n = 15) and anti-CD3ε mAb (n = 21) treated mice; ***P < .0001. (D) Representative dot plots of CD69 and TCRβ expression in DP population of indicated mice; the percentage of CD69+TCRβhigh cells is represented.

Anti-CD3ε mAb treatment induces RAG2R229Q thymic expansion and DN to DP transition, without positive selection.RAG2R229Q mice were intraperitoneally injected at the 3rd and 13th day after birth with 25 μg of anti-CD3ε mAb or PBS and killed 2 months after last injection. (A top) Macroscopic aspect of a representative RAG2R229Q thymus from mice treated with PBS or anti-CD3ε mAb. (Bottom) Length and weight of thymi from the 2 groups (n = 5); **P = .0079. (B) Absolute number of thymic cells from RAG2R229Q mice injected with PBS (n = 17) and anti-CD3ε mAb (n = 20); ***P < .0001. (C left panel) Representative dot plots of thymocyte distribution from the indicated mice. (Right panel) Graph shows the frequency of DN, DP, CD4+TCRb+ SP, and CD8+TCRβ+ SP populations in PBS (n = 15) and anti-CD3ε mAb (n = 21) treated mice; ***P < .0001. (D) Representative dot plots of CD69 and TCRβ expression in DP population of indicated mice; the percentage of CD69+TCRβhigh cells is represented.

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