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Goblet cell loss abrogates ocular surface immune tolerance
Byung Yi Ko, Yangyan Xiao, Flavia L. Barbosa, Cintia S. de Paiva, Stephen C. Pflugfelder
Byung Yi Ko, Yangyan Xiao, Flavia L. Barbosa, Cintia S. de Paiva, Stephen C. Pflugfelder
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Research Article Angiogenesis Immunology

Goblet cell loss abrogates ocular surface immune tolerance

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Abstract

Intestinal epithelial cells condition tolerogenic properties in DCs. Aqueous-deficient dry eye is associated with goblet cell (GC) loss and increased IFN-γ expression in the conjunctiva. We hypothesized that loss of GCs reduces tolerance-inducing properties of antigen presenting cells (APCs) in the conjunctiva and draining nodes. Mice lacking the SAM pointed domain containing ETS transcription factor (Spdef) that is required for GC differentiation had an increased frequency of macrophages in the conjunctiva and CD11b+CD11c+ DCs in the conjunctiva and draining nodes, and these cells had greater IL-12 expression than WT mice. Conditioned media from cultured WT conjunctival GCs suppressed LPS-induced IL-12 production by conjunctival APCs. OVA antigen–specific OTII CD4+ T cells primed by Spdef-KO draining lymph node APCs showed greater proliferation, lower frequency of Foxp3+, increased frequency of IFN-γ+ and IL-17+ cells, and greater IFN-γ production than those primed by WT APCs. The immune tolerance to OVA antigen topically applied to the conjunctiva measured by cutaneous delayed type hypersensitivity (DTH) reaction, OVA-specific T cell proliferation, Foxp3 induction, and IFN-γ production observed in WT mice was lost in the Spdef-KO mice. We concluded that conjunctival GCs condition tolerogenic properties in APCs that suppress IL-12 production and Th1 polarization.

Authors

Byung Yi Ko, Yangyan Xiao, Flavia L. Barbosa, Cintia S. de Paiva, Stephen C. Pflugfelder

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Figure 1

Lack of goblet cells alters DC distribution in Spdef-KO conjunctiva.

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Lack of goblet cells alters DC distribution in Spdef-KO conjunctiva.
(A)...
(A) Representative PAS staining of paraffin-embedded conjunctival sections. Magenta-colored PAS+ goblet cells are present in WT but absent in Spdef-KO (n = 3/group; scale bars: 50 μm). (B) Greater uptake of 70 kDa Oregon green dextran (OGD) by cornea epithelium, indicating altered corneal barrier function, was noted in the Spdef-KO (n = 8–14/group). Mean ± SEM, *P < 0.05. (C and D) Laser confocal microscopy of whole mount conjunctivas taken from fornices of WT (C) and Spdef-KO mice (D). Top left panels show surface view (200× magnification); lower left panels show distribution of DCs in the conjunctiva using Z-stack option from epithelium (e) to stroma (s). Smaller right panels are of superficial (Sup) and deep epithelium and of stroma (400× magnification). Nuclei are stained with Hoechst 33343 dye (blue) (n = 3/group). (E) Representative conjunctival sections from WT and Spdef-KO stained for CD11b (green) and DNA with propidium iodide (red, 20×). White boxes in left images are seen in higher magnification in right images (40×, n = 3/group). (F) Bar graphs of mean ± SEM of macrophage (CD11b+F4/80+) and DC (CD11c+CD11b+, CD11c+CD11b–) percentages in conjunctiva, cervical lymph nodes (CLN), and spleen from WT and Spdef-KO measured by flow cytometry. Lack of GCs increases all 3 populations in the conjunctiva and CD11c+CD11b+ DCs in the CLN of Spdef-KO (n = 4/group). Between-group comparisons for each cell type in each tissue were performed with the Student t test, *P < 0.05; **P < 0.01

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