Figure 3
Figure 3. PKR regulates clonogenic potential of BM progenitors both in vitro and in vivo. (A) Representative colonies after culture of WT, TgPKR, TgDNPKR, or PKRKO BM cells from 3- to 5-month-old mice in methylcellulose for 7 days. (B-F) Unfractionated BM cells (2 × 104 for B, C, D, and E, 105 for F) from WT, TgPKR, TgDNPKR, or PKRKO mice were plated and resulting CFU-GEMM (B), CFU-GM (C), CFU-G (D), CFU-M (E), and BFU-E (F) counted. BM from 5 mice of each genotype was assayed and mean ± SEM graphed. (G) Representative examples of macroscopic spleen colonies (CFU-S) from WT irradiated recipients injected with 2 × 104 unfractionated BM cells either from WT, TgPKR, TgDNPKR, or PKRKO mice as indicated. (H) Colonies were counted 10 days after transplantation. Graphs represent mean ± SEM (n = 4 donor mice of each genotype).

PKR regulates clonogenic potential of BM progenitors both in vitro and in vivo. (A) Representative colonies after culture of WT, TgPKR, TgDNPKR, or PKRKO BM cells from 3- to 5-month-old mice in methylcellulose for 7 days. (B-F) Unfractionated BM cells (2 × 104 for B, C, D, and E, 105 for F) from WT, TgPKR, TgDNPKR, or PKRKO mice were plated and resulting CFU-GEMM (B), CFU-GM (C), CFU-G (D), CFU-M (E), and BFU-E (F) counted. BM from 5 mice of each genotype was assayed and mean ± SEM graphed. (G) Representative examples of macroscopic spleen colonies (CFU-S) from WT irradiated recipients injected with 2 × 104 unfractionated BM cells either from WT, TgPKR, TgDNPKR, or PKRKO mice as indicated. (H) Colonies were counted 10 days after transplantation. Graphs represent mean ± SEM (n = 4 donor mice of each genotype).

Close Modal

or Create an Account

Close Modal
Close Modal