Figure 1
Figure 1. Androgen withdrawal enhances thymopoeisis as evidenced by increased thymic size, weight, and thymocyte subsets with initial increases in DN and DP and subsequent increases in mature SP populations. Panel A demonstrates that thymic weight increased significantly by 1 week after castration and was maintained for 6 months postoperatively (> 8 mice/group). Panels B-E represent absolute thymocyte counts from 6- to 8-week-old C57BL/6 male mice at various time points after castration or sham castration (6-12 mice per group). (B) Total thymocyte number dramatically rose as well within 1 week after castration and persisted for 3 months before signs of involution. Double-positive (C) and double-negative (D) thymocyte total number were significantly increased by 1 week after castration (P < .005). CD4 (E) and CD8 (F) total thymocyte number rose dramatically by one month (later than the dramatic increase in immature subsets; P < .005).

Androgen withdrawal enhances thymopoeisis as evidenced by increased thymic size, weight, and thymocyte subsets with initial increases in DN and DP and subsequent increases in mature SP populations. Panel A demonstrates that thymic weight increased significantly by 1 week after castration and was maintained for 6 months postoperatively (> 8 mice/group). Panels B-E represent absolute thymocyte counts from 6- to 8-week-old C57BL/6 male mice at various time points after castration or sham castration (6-12 mice per group). (B) Total thymocyte number dramatically rose as well within 1 week after castration and persisted for 3 months before signs of involution. Double-positive (C) and double-negative (D) thymocyte total number were significantly increased by 1 week after castration (P < .005). CD4 (E) and CD8 (F) total thymocyte number rose dramatically by one month (later than the dramatic increase in immature subsets; P < .005).

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