Figure 6
DN1 thymocytes have the capacity to migrate to the LN. (A) Bulk thymocytes from Tcrβ/Tcrδ-double-knockout mice were stained for Lin, anti-CD44, and anti-CD25 and characterized by flow analysis. (B) CFSE labeled bulk thymocytes (4 × 106) from Tcrβ/Tcrδ-double knockout mice were injected intravenously into nude mice. A day after transplantation, spleen and LN cells were stained with Lin antibody cocktail, anti-CD25, and anti-CD44 and analyzed by flow cytometry. CFSE-positive donor-derived cells were gated (left), and the percentages of DN1 (CD44+CD25−), DN2 (CD44+CD25+), and DN3 (CD44−CD25+) cells were determined (right). (C) Total donor-derived cell number seeding the spleen and LN was calculated (right), followed by number and percentage of DN1 cells within this population (middle and left).

DN1 thymocytes have the capacity to migrate to the LN. (A) Bulk thymocytes from Tcrβ/Tcrδ-double-knockout mice were stained for Lin, anti-CD44, and anti-CD25 and characterized by flow analysis. (B) CFSE labeled bulk thymocytes (4 × 106) from Tcrβ/Tcrδ-double knockout mice were injected intravenously into nude mice. A day after transplantation, spleen and LN cells were stained with Lin antibody cocktail, anti-CD25, and anti-CD44 and analyzed by flow cytometry. CFSE-positive donor-derived cells were gated (left), and the percentages of DN1 (CD44+CD25), DN2 (CD44+CD25+), and DN3 (CD44CD25+) cells were determined (right). (C) Total donor-derived cell number seeding the spleen and LN was calculated (right), followed by number and percentage of DN1 cells within this population (middle and left).

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