Figure 3.
Figure 3. Survival and proliferation of DN cells are impaired in wt LNs. (A) Analysis of cell cycle status of DN phenotype cells. Forty minutes after injection of 1 mg BrdU intraperitoneally, mice were killed and cells were stained with 7AAD and antibodies against BrdU, CD25, CD44, and lineage markers. Numbers correspond to the percentages of cells in the G1/0, S, and G2+M phase of the cell cycle. One representative experiment out of 3. (B) Lin– CD44+c-Kit subsets in cycling thymocytes. Mice received 2 injections (1 mg each) of BrdU at 2-hour intervals. Twenty-four hours later, prepared cells were stained with antibodies against BrdU, CD44, c-Kit, and lineage markers (which included CD25). Numbers indicate the percentage of BrdU+ cells. One representative experiment out of 3. (C) Percentages of annexin V+ cells in wt thymus, wt LNs, and OM+ LNs are indicated in the graphs.

Survival and proliferation of DN cells are impaired in wt LNs. (A) Analysis of cell cycle status of DN phenotype cells. Forty minutes after injection of 1 mg BrdU intraperitoneally, mice were killed and cells were stained with 7AAD and antibodies against BrdU, CD25, CD44, and lineage markers. Numbers correspond to the percentages of cells in the G1/0, S, and G2+M phase of the cell cycle. One representative experiment out of 3. (B) Lin CD44+c-Kit subsets in cycling thymocytes. Mice received 2 injections (1 mg each) of BrdU at 2-hour intervals. Twenty-four hours later, prepared cells were stained with antibodies against BrdU, CD44, c-Kit, and lineage markers (which included CD25). Numbers indicate the percentage of BrdU+ cells. One representative experiment out of 3. (C) Percentages of annexin V+ cells in wt thymus, wt LNs, and OM+ LNs are indicated in the graphs.

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