Fig. 3.
Fig. 3. Defective expression of CD25 in developingHoxa-9−/− T cells. (A) Schematic representation of normal differentiation stages within the TN population of T cells, correlated with FACS scan profiles. The curved arrow points to the stage at which TCRβ rearrangement is largely completed. (B) FACS analyses of day-15.5 fetal thymocytes was performed using antibodies against CD25 and CD44. A fourfold to fivefold reduction in the percentages of CD25+ cells (both CD44+ and CD44−) was seen in the mutant thymuses. (C) Absolute number of thymocyte subsets in fetal thymuses. Based on FACS analysis of 3 separate litters (representing 9 mutant and 12 control animals), there is an absolute decrease in all four major subsets of T cells inHoxa-9−/− thymuses, with a 25.9-fold decrease in the CD25+ compartments. (D) A representative FACS analysis of adult CD4−CD8− thymocytes. The percentage of CD25+ cells is decreased in the mutant thymus (right panel). Similar results were seen with 2 additionalHoxa-9−/− thymuses.

Defective expression of CD25 in developingHoxa-9−/− T cells. (A) Schematic representation of normal differentiation stages within the TN population of T cells, correlated with FACS scan profiles. The curved arrow points to the stage at which TCRβ rearrangement is largely completed. (B) FACS analyses of day-15.5 fetal thymocytes was performed using antibodies against CD25 and CD44. A fourfold to fivefold reduction in the percentages of CD25+ cells (both CD44+ and CD44) was seen in the mutant thymuses. (C) Absolute number of thymocyte subsets in fetal thymuses. Based on FACS analysis of 3 separate litters (representing 9 mutant and 12 control animals), there is an absolute decrease in all four major subsets of T cells inHoxa-9−/− thymuses, with a 25.9-fold decrease in the CD25+ compartments. (D) A representative FACS analysis of adult CD4CD8 thymocytes. The percentage of CD25+ cells is decreased in the mutant thymus (right panel). Similar results were seen with 2 additionalHoxa-9−/− thymuses.

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