Fig. 3From: Novel alterations in corneal neuroimmune phenotypes in mice with central nervous system tauopathyDendritic cells in the central and peripheral corneal epithelium of WT and rTg4510 mice at 2, 6, 8, and 11 months. a–f Representative images of CD45+ DCs show higher abundance in the peripheral versus central cornea for both genotypes, with few DCs across the peripheral area in rTg4510 mice at 11 months (d–f). c, f In rTg4510 mice, CD45+ DCs had an altered, amoeboid morphology compared to WT at 11 months. g The central cornea showed no significant inter-group differences at any age (P > 0.05). h Substantial differences were observed in the peripheral cornea, whereby there was a significantly lower DC density in rTg4510 mice compared to WT mice, at both 8 and 11 months (P < 0.05). i–p DCs were analyzed for field area, cell area, total dendrite length (TDL), and number of dendrites per cell. There was no genotype difference in the central cornea except for a larger cell area in the 8-month-old WT mice compared to rTg4510 mice (j, P < 0.05). m–p In the peripheral cornea, DC field areas were significantly smaller in rTg4510 mice compared to WT, at 6, 8, and 11 months of age (m, P < 0.05). Cell area analysis shows no significant genotype difference (n). TDL and number of dendrites per cell were less in the 11-month-old rTg4510 mice compared to WT (o, p; P < 0.05). q Morphometric methods for field area, cell area, TDL, and number of dendrites per cell. Scale bars represent 100 μm. Date are shown as mean ± SEM, where * indicates P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001 as determined using the two-way ANOVA and Tukey’s multiple comparisonsBack to article page