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. 2013 Jun 27;22(22):4579–4590. doi: 10.1093/hmg/ddt307

Figure 5.

Figure 5.

Corneal oedema and progressive corneal dysfunction in slc4A-a11−/− mice. (A) Slit lamp examination of WT and slc4a11−/− mice. Corneas of 48-week WT and slc4a11−/− mice seen under retro-illumination (top panels) and examined using tangential slit illumination (bottom panels). Arrows indicate corneal haze observed in slc4a11−/− mice. (B) Corneal thickness measured by in vivo confocal microscopy (n = 5 per genotype). Central corneal thickness was significantly different between WT and slc4a11−/− mice at all time points (P < 0.01). The corneal thickness in heterozygous (slc4a11+/−) mice was not different compared with wild-type mice. (C) Scanning electron micrographs of corneal endothelia from WT and slc4a11−/−mice at 32 weeks. Scale bars are 20 µm. (D) Statistical analysis of corneal endothelial cell density.