Figure 1.
Effect of p18 knockdown on human hematopoietic cells. Representative images (A) and absolute numbers (B) of the flow cytometry data of human CD34+ and CD34+CD49f+ cell populations of hUCB CD34+ cells after infection of lentivirus carrying hairpin RNA targeting p18 were measured at 7 days (n = 3); 1 × 104 CD34+GFP+ human UCB cells were seeded at the beginning. (C) Total CFC contents of control and p18 knockdown human CD34+ cells at 2 weeks (n = 3). GEMM, colony-forming unit-granulocyte, erythroid, macrophage, megakaryocyte; CFU-GM, colony-forming unit-granulocyte, macrophage; BFU-E, burst-forming unit-erythroid; CFU-E, colony-forming unit-erythroid. (D) Frequencies of CAFCs of control and p18 knockdown human CD34+ cells (n = 10). Doses of 30 000, 15 000, 7500, 3750, and 1875 cells per well were used. The experiment was repeated 3 times. All data represent the means ± standard deviation (SD). Compared with control unless specified: *P < .05, **P < .01, ***P < .001 by 2-tailed unpaired t test.

Effect of p18 knockdown on human hematopoietic cells. Representative images (A) and absolute numbers (B) of the flow cytometry data of human CD34+ and CD34+CD49f+ cell populations of hUCB CD34+ cells after infection of lentivirus carrying hairpin RNA targeting p18 were measured at 7 days (n = 3); 1 × 104 CD34+GFP+ human UCB cells were seeded at the beginning. (C) Total CFC contents of control and p18 knockdown human CD34+ cells at 2 weeks (n = 3). GEMM, colony-forming unit-granulocyte, erythroid, macrophage, megakaryocyte; CFU-GM, colony-forming unit-granulocyte, macrophage; BFU-E, burst-forming unit-erythroid; CFU-E, colony-forming unit-erythroid. (D) Frequencies of CAFCs of control and p18 knockdown human CD34+ cells (n = 10). Doses of 30 000, 15 000, 7500, 3750, and 1875 cells per well were used. The experiment was repeated 3 times. All data represent the means ± standard deviation (SD). Compared with control unless specified: *P < .05, **P < .01, ***P < .001 by 2-tailed unpaired t test.

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