Europe PMC requires Javascript to function effectively.
Either your web browser doesn't support Javascript or it is currently turned off. In the latter case, please
turn on Javascript support in your web browser and reload this page.
Figure 1
Goblet cell-associated antigen passage (GAP) formation is inhibited by Salmonella in a MyD88 and EGFR dependent manner(a) Fluorescent images of SI villus cross section of C57BL/6 mice given luminal 10kD dextran (red) and DAPI (blue), one hour after receiving luminal PBS (left), 5×108 CFU invasion deficient Salmonella (ΔinvG Sal; center) or 5×108 CFU wildtype Salmonella (WT-Sal; right). (b) Density of GAPs in C57BL/6 mice, given 5×108 CFU or wildtype or ΔinvG Salmonella in the SI lumen 1 hr earlier (left panel) or given 5×107 CFU wildtype or ΔinvG Salmonella orally 2 days earlier (right panel). (c) MyD88fl/fl Math1Cre*PR and (d) EGFRf/f Math1Cre*PR mice and littermate controls were treated with RU486 to delete MyD88 or EGFR from GCs and were administered with 5×108 CFU of wildtype Salmonella or PBS for 1 hour within the SI-lumen (left panel), or gavaged with 5×107 CFU wildtype Salmonella and SI tissue sections were evaluated 2 days later (right panel). Graphs depict the density of GAPs in SI villus cross section of uninfected and infected mice. Data represented as the mean ± SEM. Scale bar in a= 50 μm. *p<0.05, ns = not significant. n=5 or more mice with 60 or more villus cross sections per mouse examined for each condition.
Images in this article
Click on the image to see a larger version.