Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
  • Physician-Scientist Development
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • In-Press Preview
    • Resource and Technical Advances
    • Clinical Research and Public Health
    • Research Letters
    • Editorials
    • Perspectives
    • Physician-Scientist Development
    • Reviews
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • In-Press Preview
  • Resource and Technical Advances
  • Clinical Research and Public Health
  • Research Letters
  • Editorials
  • Perspectives
  • Physician-Scientist Development
  • Reviews
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
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
View: Text | PDF
Research Article Angiogenesis Immunology

Goblet cell loss abrogates ocular surface immune tolerance

  • Text
  • PDF
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

×

Figure 3

Increased IL-12 production in conjunctiva of Spdef-KO mice.

Options: View larger image (or click on image) Download as PowerPoint
Increased IL-12 production in conjunctiva of Spdef-KO mice.
(A) Immunohi...
(A) Immunohistochemical staining demonstrates presence of IL-12α+ cells in the conjunctiva of Spdef-KO mice. Slides without primary antibody are shown as negative control (neg. control). Scale bars: 50 μm. Arrows indicate IL-12+ cells. Magnification of inset, 2× (B) Flow cytometry analysis showing percentage and median fluorescence intensity (MFI) of IL-12+ macrophages (CD11b+F4/80+) and DCs (CD11c+CD11b+, CD11c+CD11b–) in conjunctiva of WT and Spdef-KO (n = 3/group, means ± SEM, between-group comparisons for each cell type performed with Mann-Whitney test). (C) Graphs showing percentage and MFI of IL-12+CD11c+CD11b+ (left) or CD11b+F4/80+ (right) cells in Spdef-KO mice with or without topical administration of media (IMDM) or CjCM prior to topical LPS challenge. Mice received a single dose of media as noted 1 hour (1×) or 1 day and 1 hour (for a total of 5 applications) prior to LPS stimulation. (n = 6/group, means ± SEM, 1-way ANOVA followed by Holm-Sidak’s multiple comparisons test corrected for repeated measures). (D) Histograms of median fluorescence intensity (MFI) of IL-12+CD11c+CD11b+ cells in conjunctivae of Spdef-KO treated topically with water, LPS, and IMDM (media control) 5× prior to LPS or WT conjunctival conditioned media (CjCM) 5× prior to LPS.

Copyright © 2026 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts