Figure 7
Figure 7. Analysis of in vitro colony-forming capacity, apoptosis, and proliferation of HPCs from Apc-heterozygous mice. (A) In vitro colony-forming assays. The number of BM CFU-GEMM, CFU-GM, CFU-G, CFU-M, and BFU-E was examined in Mx1-Cre+Apcfl/+ or Mx1-Cre−Apcfl/+mice 2 months after induction (mean ± SD of 3 animals). *P < .05. (B-C) Frequency of (B) apoptosis and (C) proliferation in gated HPCs (Lin− Kit+ Sca-1− Il-7R−) stained with Annexin V and DAPI, or DAPI, respectively, from Mx1-Cre+Apcfl/+ and Mx1-Cre−Apcfl/+ mice 3 to 4 months after pI-pC induction (mean ± SD of 3 animals). *P < .05; **P = .057.

Analysis of in vitro colony-forming capacity, apoptosis, and proliferation of HPCs from Apc-heterozygous mice. (A) In vitro colony-forming assays. The number of BM CFU-GEMM, CFU-GM, CFU-G, CFU-M, and BFU-E was examined in Mx1-Cre+Apcfl/+ or Mx1-CreApcfl/+mice 2 months after induction (mean ± SD of 3 animals). *P < .05. (B-C) Frequency of (B) apoptosis and (C) proliferation in gated HPCs (Lin Kit+ Sca-1 Il-7R) stained with Annexin V and DAPI, or DAPI, respectively, from Mx1-Cre+Apcfl/+ and Mx1-CreApcfl/+ mice 3 to 4 months after pI-pC induction (mean ± SD of 3 animals). *P < .05; **P = .057.

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