Figure 3
Figure 3. The Cdk4 R24C allele rescues defective progenitor potential in Cdk6 R31C mice. (A) Analysis of the donor cells’ contribution within the LSK fraction 16 weeks after bone marrow transplantation (n = 5 for wild-type, Cdk4R/R or Cdk6R/R single mutants; n = 4 double-mutant mice). (B) Analysis of the donor contribution to individual lineages in bone marrow, spleen, and peripheral blood (n = 5 for wild-type, Cdk4R/R or Cdk6R/R single mutants; n = 4 double-mutant mice). (C) Analysis of bone marrow repopulation after 5-FU treatment. Flow cytometry analysis of hematopoietic progenitors (LSK cells) 7 days after treatment with 5-FU (n = 3 Cdk4R/R or Cdk6R/R single mutants; n = 6 wild-type mice; n = 7 double-mutant mice). Representative hematoxylin and eosin images of the bone marrow from untreated mice or mice treated with 5-FU mice are included. DMSO, dimethylsulfoxide. Scale bars, 50 μm. *P < .05; **P < .01; ***P < .001. 1-way ANOVA including Bonferroni’s multiple comparison test.

The Cdk4 R24C allele rescues defective progenitor potential in Cdk6 R31C mice. (A) Analysis of the donor cells’ contribution within the LSK fraction 16 weeks after bone marrow transplantation (n = 5 for wild-type, Cdk4R/R or Cdk6R/R single mutants; n = 4 double-mutant mice). (B) Analysis of the donor contribution to individual lineages in bone marrow, spleen, and peripheral blood (n = 5 for wild-type, Cdk4R/R or Cdk6R/R single mutants; n = 4 double-mutant mice). (C) Analysis of bone marrow repopulation after 5-FU treatment. Flow cytometry analysis of hematopoietic progenitors (LSK cells) 7 days after treatment with 5-FU (n = 3 Cdk4R/R or Cdk6R/R single mutants; n = 6 wild-type mice; n = 7 double-mutant mice). Representative hematoxylin and eosin images of the bone marrow from untreated mice or mice treated with 5-FU mice are included. DMSO, dimethylsulfoxide. Scale bars, 50 μm. *P < .05; **P < .01; ***P < .001. 1-way ANOVA including Bonferroni’s multiple comparison test.

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