Fig. 1.
Fig. 1. Importance of ov chimerism in the thymus depends on the number of injected T-cell progenitors. (A) BM cells derived from E13 H.B19 animals stained for c-kit and HEMCAM. The FACS profile shows BM gated for lymphoid cells in the forward and side scatter. HEMCAM+ lymphoid cells represented 10% of total BM cells and 50% of lymphoid cells. (B) Percentage of ov+ donor thymocytes when increasing numbers of total (□), HEMCAM+ sorted (▪), and HEMCAM+c-kit+ sorted (○) E13 BM cells were injected into irradiated chicks. (C) Determination of T-cell precursor frequency in HEMCAM+ c-kit+ E13 BM population by limiting dilution analysis. Titrated numbers of BM cell populations were injected intrathymically into ov− recipients and the thymus was assayed 2 weeks later for ov+ cells by flow cytometry using MoAb 11A9. These data were obtained after injection of 12 cells, 20 cells, 40 cells into 5, 7, and 12 recipients, respectively.

Importance of ov chimerism in the thymus depends on the number of injected T-cell progenitors. (A) BM cells derived from E13 H.B19 animals stained for c-kit and HEMCAM. The FACS profile shows BM gated for lymphoid cells in the forward and side scatter. HEMCAM+ lymphoid cells represented 10% of total BM cells and 50% of lymphoid cells. (B) Percentage of ov+ donor thymocytes when increasing numbers of total (□), HEMCAM+ sorted (▪), and HEMCAM+c-kit+ sorted (○) E13 BM cells were injected into irradiated chicks. (C) Determination of T-cell precursor frequency in HEMCAM+ c-kit+ E13 BM population by limiting dilution analysis. Titrated numbers of BM cell populations were injected intrathymically into ov recipients and the thymus was assayed 2 weeks later for ov+ cells by flow cytometry using MoAb 11A9. These data were obtained after injection of 12 cells, 20 cells, 40 cells into 5, 7, and 12 recipients, respectively.

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