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. Author manuscript; available in PMC: 2022 Mar 1.
Published in final edited form as: Radiat Res. 2021 Mar 1;195(3):301–306. doi: 10.1667/RADE-20-00221.1

FIG. 2.

FIG. 2.

Unirradiated bone marrow cells suppress the formation of radiation-induced thymic lymphoma through niche competition. Four-week-old B6.SJL (CD45.1) mice received one dose of 1.8 Gy TBI for four consecutive weeks. Bone marrow transplantation (BMT) was performed 6 h after final TBI. Each recipient was intravenously injected with 1 × 107 bone marrow cells from mice on a CD45.2 background. Both male and female mice were used. Panel A: Lymphoma-free survival of irradiated mice that received bone marrow cells from either wild-type (WT) or Rag2−/−; γc−/− mice or did not receive bone marrow cells (No BMT). P = 0.0004 for WT BM vs. no BMT; P = 0.0071 for WT BM vs. Rag2−/−; γc−/− BM; P = 0.2553 for Rag2−/−; γc−/− BM vs. no BMT. P value was calculated using log-rank test. Panel B: Lymphoma-free survival of irradiated mice that received bone marrow cells from Rag2−/−; γc−/− or Rag2−/− mice. These data are the summary of results from three independent experiments. P value was calculated using log-rank test. Panel C: Bone marrow cells and thymocytes were harvested to examine the repopulation of donor-derived cells by flow cytometry. Donor-derived repopulation was examined in LSK (Lineage Sca1+ cKit+) cells in the BM as well as DN2 (CD4 CD8 CD25+ CD44+), DN3 (CD4 CD8 CD25+ CD44), DN4 (CD4 CD8 CD25 CD44), DP (CD4+ CD8+), CD8SP (CD8+) and CD4SP (CD4+) thymocytes. n = 5 mice for wild-type and n = 7 mice for Rag2−/−. Data are presented as mean 6 SE. *P < 0.05 (two-tailed t test). Panel D. Lymphoma-free survival of irradiated mice that received bone marrow cells from Rag2−/−; γc−/− or IgM−/− mice. P value was calculated by log-rank test.