Figure 1
Figure 1. Deletion of Puma renders mice resistant to γ-irradiation. (A) Kaplan-Meier survival curves of mice exposed to 9 Gy TBI. Puma+/+ (n = 9), Puma+/− (n = 6), and Puma−/− (n = 8) mice were given a single dose of TBI (9 Gy) and were monitored for survival. The enhanced survival rate of Puma−/− and Puma+/− mice was significantly greater than Puma+/+ mice (P < .001 and P < .01, respectively), but the survival rate was not significantly different between Puma−/− mice versus Puma+/− mice (P > .05). (B) Kaplan-Meier survival curves of mice exposed to 9.5 Gy TBI. Puma+/+ (n = 6), Puma+/− (n = 9), and Puma−/− (n = 7) mice were then administrated a lethal TBI dose (9.5 Gy) and monitored daily for survival. The survival rate of Puma−/− and Puma+/− mice was significantly greater than Puma+/+ mice (Puma−/− mice vs Puma+/+ mice, P < .001; Puma+/− mice vs Puma+/+ mice, P < .01). (C) Diagram for generation of reconstituted mice. C57BL6/N recipients were lethally irradiated for a total of 13 Gy (6.5 Gy, 2 times, 3 hours apart) and received 1 × 107 total BM cells from Puma+/+ mice or Puma−/− mice (n = 6 mice/group). (D) Kaplan-Meier survival curves of reconstituted mice after 9 Gy TBI. After 8 weeks, the mice in panel C were given a second course of TBI (9 Gy) and monitored for survival. The survival rate of mice reconstituted with Puma−/− BM cells was significantly higher than in mice reconstituted with Puma+/+ BM cells (P < .001).

Deletion of Puma renders mice resistant to γ-irradiation. (A) Kaplan-Meier survival curves of mice exposed to 9 Gy TBI. Puma+/+ (n = 9), Puma+/− (n = 6), and Puma−/− (n = 8) mice were given a single dose of TBI (9 Gy) and were monitored for survival. The enhanced survival rate of Puma−/− and Puma+/− mice was significantly greater than Puma+/+ mice (P < .001 and P < .01, respectively), but the survival rate was not significantly different between Puma−/− mice versus Puma+/− mice (P > .05). (B) Kaplan-Meier survival curves of mice exposed to 9.5 Gy TBI. Puma+/+ (n = 6), Puma+/− (n = 9), and Puma−/− (n = 7) mice were then administrated a lethal TBI dose (9.5 Gy) and monitored daily for survival. The survival rate of Puma−/− and Puma+/− mice was significantly greater than Puma+/+ mice (Puma−/− mice vs Puma+/+ mice, P < .001; Puma+/− mice vs Puma+/+ mice, P < .01). (C) Diagram for generation of reconstituted mice. C57BL6/N recipients were lethally irradiated for a total of 13 Gy (6.5 Gy, 2 times, 3 hours apart) and received 1 × 107 total BM cells from Puma+/+ mice or Puma−/− mice (n = 6 mice/group). (D) Kaplan-Meier survival curves of reconstituted mice after 9 Gy TBI. After 8 weeks, the mice in panel C were given a second course of TBI (9 Gy) and monitored for survival. The survival rate of mice reconstituted with Puma−/− BM cells was significantly higher than in mice reconstituted with Puma+/+ BM cells (P < .001).

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