Fig. 2.
Fig. 2. Assessment of alloengraftment in central (BM, thymus) and peripheral (spleen) lymphohematopoietic compartments. BM (A), thymus (B), and spleen (C) was obtained from 4- to 6-month-old chimeras (n = 5 to 6 mice/group) and analyzed for the presence of donor cells. In BM and spleen, the number of donor CD4+, CD8+, CD19+ B cells, donor Mac1+(Mac1b), and host Mac1+ (Mac1d) cells were quantified. The thymus was analyzed for T-cell differentiation consisting of immature CD4−8−, intermediate CD4+8+, and mature CD4+8− or CD4−8+ cells. The absolute number of cells is shown on the y-axis. One standard error of the mean values for absolute cell number are designated by bars. *Significant differences between IUT TCD recipients and other groups. #Significant differences between the indicated groups and the non-BMT B6 control mice.

Assessment of alloengraftment in central (BM, thymus) and peripheral (spleen) lymphohematopoietic compartments. BM (A), thymus (B), and spleen (C) was obtained from 4- to 6-month-old chimeras (n = 5 to 6 mice/group) and analyzed for the presence of donor cells. In BM and spleen, the number of donor CD4+, CD8+, CD19+ B cells, donor Mac1+(Mac1b), and host Mac1+ (Mac1d) cells were quantified. The thymus was analyzed for T-cell differentiation consisting of immature CD48, intermediate CD4+8+, and mature CD4+8 or CD48+ cells. The absolute number of cells is shown on the y-axis. One standard error of the mean values for absolute cell number are designated by bars. *Significant differences between IUT TCD recipients and other groups. #Significant differences between the indicated groups and the non-BMT B6 control mice.

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