Figure 3
Figure 3. Androgen withdrawal increases UEA+ thymic epithelial cell proliferation. Six-week-old male mice were treated with 2 mg of BrdU i.p. on day 1 and 0.08% BrdU p.o. continuously for 7 days after castration or sham castration. Data represent 5 experiments with 3 thymi pooled per group for digestion. TEC populations were enumerated by flow cytometry, with medullary TEC defined as CD45− UEA+, cortical TEC as CD45− Ly51+, and a double-negative population of CD45− UEA− Ly51−. Representative flow cytometry plots are shown for gating of CD45 negative population (A) and discrimination of medullary and cortical populations within the CD45− population (B). BrdU-negative populations were defined using a noncastrated control group that underwent TEC preparation and were stained with BrdU antibody but did not receive exogenous BrdU. (C) Graph represents the mean frequency of BrdU + populations with standard error bars.

Androgen withdrawal increases UEA+ thymic epithelial cell proliferation. Six-week-old male mice were treated with 2 mg of BrdU i.p. on day 1 and 0.08% BrdU p.o. continuously for 7 days after castration or sham castration. Data represent 5 experiments with 3 thymi pooled per group for digestion. TEC populations were enumerated by flow cytometry, with medullary TEC defined as CD45 UEA+, cortical TEC as CD45 Ly51+, and a double-negative population of CD45 UEA Ly51. Representative flow cytometry plots are shown for gating of CD45 negative population (A) and discrimination of medullary and cortical populations within the CD45 population (B). BrdU-negative populations were defined using a noncastrated control group that underwent TEC preparation and were stained with BrdU antibody but did not receive exogenous BrdU. (C) Graph represents the mean frequency of BrdU + populations with standard error bars.

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