Figure 4
Figure 4. Rps19 deficiency results in impaired proliferation of hematopoietic progenitors and increased apoptosis. shRNA-B mice were induced for 10 days with doxycycline followed by FACS sorting of (A) preMegE progenitors (n = 180 single-cell cultures), (B) preCFU-E/CFU-E progenitors (n = 240 single-cell cultures) or (C) 1000 preGM/GMP progenitors (n = 3-6 per genotype) into supportive liquid cultures with or without doxycycline. (D) Cell cycle analysis of early (CD71+ Ter119+) and late (CD71low Ter119+) erythroblasts in induced shRNA-B mice (n = 4-6 per genotype). Dean-Jett-Fox model was used to calculate percentages of cells in G1/G0, S, and G2/M phases (shown in green). (E) TUNEL staining of whole bone marrow cells from shRNA-B mice after 10 days (n = 2-3 per genotype) or 7 weeks (n = 3 per genotype) of doxycycline administration. Error bars represent SD.

Rps19 deficiency results in impaired proliferation of hematopoietic progenitors and increased apoptosis. shRNA-B mice were induced for 10 days with doxycycline followed by FACS sorting of (A) preMegE progenitors (n = 180 single-cell cultures), (B) preCFU-E/CFU-E progenitors (n = 240 single-cell cultures) or (C) 1000 preGM/GMP progenitors (n = 3-6 per genotype) into supportive liquid cultures with or without doxycycline. (D) Cell cycle analysis of early (CD71+ Ter119+) and late (CD71low Ter119+) erythroblasts in induced shRNA-B mice (n = 4-6 per genotype). Dean-Jett-Fox model was used to calculate percentages of cells in G1/G0, S, and G2/M phases (shown in green). (E) TUNEL staining of whole bone marrow cells from shRNA-B mice after 10 days (n = 2-3 per genotype) or 7 weeks (n = 3 per genotype) of doxycycline administration. Error bars represent SD.

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