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. 2019 Mar 4;11(4):e9976. doi: 10.15252/emmm.201809976

Figure 2. Reduced tumor cell proliferation and inflammation in Kras G12D:Adam17 ex/ex mouse lungs.

Figure 2

  • A
    Representative images of PCNA‐stained lung sections from Kras WT, Kras G12D, and Kras G12D:Adam17 ex/ex mice at 6 weeks post‐Ad‐Cre (for Kras G12D) or vehicle (for Kras WT) inhalation. Scale bar, 100 μm.
  • B
    Quantification of PCNA‐positive cells/high‐power field (HPF) in the indicated mouse lungs (n = 6 per genotype). **< 0.01, Student's t‐test, mean ± SEM.
  • C
    qPCR expression analyses of cell cycle regulation genes (normalized against 18SrRNA) in lungs from the indicated mice (n = 6 per genotype). *< 0.05, Student's t‐test, mean ± SEM.
  • D
    Representative immunoblots of Kras G12D and Kras G12D:Adam17 ex/ex lung lysates with the indicated antibodies. Each lane is an individual mouse sample.
  • E
    Semi‐quantitative densitometry of Myc protein levels (relative to actin) in lung lysates from (D). n = 6 per genotype. **< 0.01, Student's t‐test, mean ± SEM.
  • F, G
    Representative images (F) and quantification of CD45‐positive cells/HPF (G) in CD45‐stained lung sections from the indicated genotypes at 6 weeks post‐inhalations, mean ± SEM. In (F), scale bar, 100 μm. In (G), n = 6 per genotype. **< 0.01, Student's t‐test.
Data information: Exact P values are specified in Appendix Table S4.Source data are available online for this figure.