Fig. 6.
Fig. 6. Early expansion of CD4+ donor T cells depends on FasL function. / Highly enriched CD4+ T cells were obtained from spleens of B6, B6-pko, B6-gld, and B6-cdd mice by means of magnetic beads on Macs column (see “Materials and methods”). Then, 1 × 106donor CD4+ T cells were combined with 5 × 106 T-cell–depleted B6-Ly5.1 bone marrow cells and injected into BALB/c recipients (2 per group) irradiated at 5.5-Gy (A) or 11-Gy (B) TBI 24 hours earlier. At day 5, the mesenteric lymph nodes were harvested from individual recipient mice and counted. Donor T cells were identified by staining with anti-CD4, anti–H-2Kb, and anti-Ly5.1 mAbs. The percentage of CD4+H-2Kb+Ly5.1− cells × the total number of nucleated lymph node cells was used to determine donor cell numbers. (A) B6-cdd and B6-gld versus B6: P < .0014. B6-pko versus B6: P > .5. (B) B6-cdd, B6-gld, and B6-pko versus B6-wt: P > .5.

Early expansion of CD4+ donor T cells depends on FasL function.

Highly enriched CD4+ T cells were obtained from spleens of B6, B6-pko, B6-gld, and B6-cdd mice by means of magnetic beads on Macs column (see “Materials and methods”). Then, 1 × 106donor CD4+ T cells were combined with 5 × 106 T-cell–depleted B6-Ly5.1 bone marrow cells and injected into BALB/c recipients (2 per group) irradiated at 5.5-Gy (A) or 11-Gy (B) TBI 24 hours earlier. At day 5, the mesenteric lymph nodes were harvested from individual recipient mice and counted. Donor T cells were identified by staining with anti-CD4, anti–H-2Kb, and anti-Ly5.1 mAbs. The percentage of CD4+H-2Kb+Ly5.1 cells × the total number of nucleated lymph node cells was used to determine donor cell numbers. (A) B6-cdd and B6-gld versus B6: P < .0014. B6-pko versus B6: P > .5. (B) B6-cdd, B6-gld, and B6-pko versus B6-wt: P > .5.

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