Fig. 2.
Fig. 2. Thymocyte differentiation in ZAP-70−/− mice undergoing transplantation with ZAP-70 genecorrected BM cells. / Thymocytes were harvested from euthanized animals at 18 weeks after BMT and analyzed by flow cytometry. (A) Thymocytes were stained with PE-conjugated αCD8 and Cy-conjugated αCD4 mAbs. The percentages of CD4+ and CD8+ SP thymocytes are indicated in each dot plot. (B) As a measure of thymocyte differentiation, expression of CD5 and TCRβ was assessed in the EGFP− and EGP+ thymocyte populations of ZAP-70−/− mice undergoing transplantation with control EGFP or ZAP-70/EGFP retroviral vectors. Expression of these 2 markers was also monitored in the total thymocyte population of WT mice and ZAP-70−/− mice undergoing transplantation with WT BM. The percentages of CD5hi and TCRβhi cells are indicated. Histograms are representative of data obtained from 3 to 4 mice in each group.

Thymocyte differentiation in ZAP-70−/− mice undergoing transplantation with ZAP-70 genecorrected BM cells.

Thymocytes were harvested from euthanized animals at 18 weeks after BMT and analyzed by flow cytometry. (A) Thymocytes were stained with PE-conjugated αCD8 and Cy-conjugated αCD4 mAbs. The percentages of CD4+ and CD8+ SP thymocytes are indicated in each dot plot. (B) As a measure of thymocyte differentiation, expression of CD5 and TCRβ was assessed in the EGFP and EGP+ thymocyte populations of ZAP-70−/− mice undergoing transplantation with control EGFP or ZAP-70/EGFP retroviral vectors. Expression of these 2 markers was also monitored in the total thymocyte population of WT mice and ZAP-70−/− mice undergoing transplantation with WT BM. The percentages of CD5hi and TCRβhi cells are indicated. Histograms are representative of data obtained from 3 to 4 mice in each group.

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