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. 2019 Dec 3;12(2):e10862. doi: 10.15252/emmm.201910862

Figure 2. MT1‐MMP absence from endothelial cells limits deterioration of vascular perfusion and impedes colitis progression.

Figure 2

  • A
    Representative maximum‐intensity projection images of whole‐mount distal colons stained for CD31 (green) and IB4 (red) in MT1f/f and MT1iΔEC mice left untreated (basal) or treated with 1% DSS for 3 or 7 days. Scale bar, 40 μm.
  • B
    Perfusion decreased during 1% DSS‐induced colitis in MT1f/f and MT1iΔEC mice; n = 8–12 mice per genotype and condition. Data are shown as mean ± SEM and were tested by one‐way ANOVA with Benjamini and Hochberg post‐test; **P < 0.01.
  • C
    Representative H&E‐stained colon sections from MT1f/f and MT1iΔEC mice left untreated (basal) or treated with 1% DSS for 3 or 7 days. Arrows indicate crypt destruction. Scale bar, 50 μm.
  • D
    Representative second‐harmonic generation (SHG) microscopy images of mucosal plexus in whole‐mount colons from MT1f/f or MT1iΔEC mice left untreated (basal) or treated with 1% DSS for 3 or 7 days. Scale bar, 40 μm.
  • E
    Disease activity index (DAI, a composite of weight change, stool consistency, and presence of fecal blood) during 1% DSS‐induced colitis in MT1f/f and MT1iΔEC mice. Untreated mice were included as a control. n = 19–24 per genotype and condition. Data are shown as mean ± SEM and were tested by two‐way ANOVA with Benjamini and Hochberg post‐test; ***P < 0.001.
Data information: Please see Appendix Table S3 for exact P‐values.Source data are available online for this figure.