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Masaru Yoshida, Kanna Kobayashi, Timothy T. Kuo, Lynn Bry, Jonathan N. Glickman, Steven M. Claypool, Arthur Kaser, Takashi Nagaishi, Darren E. Higgins, Emiko Mizoguchi, Yoshio Wakatsuki, Derry C. Roopenian, Atsushi Mizoguchi, Wayne I. Lencer, Richard S. Blumberg
Published in Volume 116, Issue 8
J Clin Invest. 2006; 116(8):2142–2151 doi:10.1172/JCI27821
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Figure 5
Luminal bacterial antigens transported as an immune complex across intestinal epithelial cells via FcRn in vivo.

(A and B) Flow cytometry of rabbit anti–E. coli IgG and control IgG followed by PE-conjugated goat anti-rabbit IgG (A) and FITC-conjugated E. coli (B). (CF) Confocal microscopy analysis of transport of bacterial antigens across intestinal epithelial cells. Sections were stained for actin (phalloidin; red) and nuclei (blue). Magnification, ×400. Arrow in F illustrates transported FITC-conjugated E. coli in intestinal epithelial cells in the presence of rabbit anti–E. coli IgG. (G) Presence of FITC-conjugated E. coli in CD11c+ cells of the MLNs of IFABP-mFcRnTg/mβ2mTg/FcRn–/– mice 5 hours after FITC-conjugated E. coli administration in the presence of rabbit anti–E. coli IgG. Mean fluorescence intensity (MFI) on gated CD11c+ cells is shown. The mean ± SD was shown for each group (n = 4). *P < 0.05.