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. 2020 Mar 9;21(4):e48389. doi: 10.15252/embr.201948389

Figure 7. Hoxa4 KO mice alleviate smooth muscle phenotypic modulation and abrogate neointima formation after carotid artery ligation injury.

Figure 7

  • A
    Quantitative real‐time PCR analysis of differentiated smooth muscle marker genes in the left carotid artery of 8‐week‐old WT and Hoxa4 KO mice (WT: n = 7; Hoxa4 KO: n = 5).
  • B
    Quantitative real‐time PCR analysis of differentiated smooth muscle marker genes in the ligated left carotid artery of WT and Hoxa4 KO mice at 1 week after ligation (n = 6). Mean expression level of six WT mice at the baseline was defined as 1.0.
  • C
    Hoxa4 expression levels in the ligated left carotid artery of WT mice at 1 week after ligation (n = 6).
  • D
    Quantitative real‐time PCR analysis of Yap/Tead target genes in the left carotid artery of 8‐week‐old WT and Hoxa4 KO mice (WT: n = 7; Hoxa4 KO: n = 5).
  • E
    Quantitative real‐time PCR analysis of Yap/Tead target genes in the ligated left carotid artery of WT and Hoxa4 KO mice at 1 week after ligation (n = 6). Mean expression level of six WT mice at the baseline was defined as 1.0.
  • F
    Representative Western blotting analysis and densitometry of non‐ligated (right; R) and ligated (left; L) carotid arteries from WT and Hoxa4 KO mice at 1 week after ligation (WT: n = 6; Hoxa4 KO: n = 7). *P < 0.05, **P < 0.01, by two‐way ANOVA with Sidak's correction.
  • G–I
    Representative images showing Elastica van Gieson staining (G); vessel, neointima, and media area (H); and neointima‐to‐media layer ratio (I) of carotid arteries of WT and Hoxa4 KO mice at 4 weeks after ligation (WT: n = 14; Hoxa4 KO: n = 11).
Data information: Images and data were obtained at 250 μm proximal to the ligation. Scale bars indicate 100 μm. *P < 0.05, **P < 0.01 versus WT, except in (C) versus baseline, by unpaired two‐tailed Mann–Whitney test. Data are presented as mean ± SEM. N.D., not detected.