Role of oncostatin M in the pathogenesis of vernal keratoconjunctivitis: focus on tissue remodeling

Purpose Vernal keratoconjunctivitis (VKC) is a severe and recurrent allergic conjunctivitis, the mechanism of which is not well understood. In this study, we investigated the role of oncostatin M (OSM) in the pathogenesis of VKC, with a focus on tissue remodeling. Study design Clinical and experimental. Patients and methods The OSM concentrations in tear fluid samples obtained from VKC patients and healthy controls were measured using ELISA, and the expression of OSM mRNA and protein in giant papillae resected from VKC patients was investigated using RT-PCR and immunohistochemistry, respectively. In cultured human conjunctival epithelial cells (HconEpiCs), expression of OSM receptor beta (OSMR beta) was detected using immunocytochemical and FACS analyses. Finally, we investigated whether recombinant OSM activated STAT1 and STAT3 to induce the expression of various genes related to tissue remodeling in HconEpiCs, by using Western blot analysis, microarray analysis, and RT-PCR. Results The OSM concentration was higher in the tear fluid of VKC patients than in that of the healthy controls, and strong expression of OSM mRNA was found in the giant papillae. We also detected T cells expressing OSM in the giant papillae. In addition, HconEpiCs showed surface expression of OSMR beta. Recombinant human OSM strongly activated both STAT1 and STAT3 in HconEpiCs and induced various tissue remodeling-related genes, including MMP-1, MMP-3, IL-24, IL-20, serpinB3, S100A7, tenascin C, and SOCS3. Conclusion Our results suggest that OSM is one of the key molecules involved in remodeling of giant papillae in VKC.

Automated summary

The study found that the concentration of OSM in the tear fluid of VKC patients was higher than that of healthy controls, and strong expression of OSM mRNA was found in giant papillae. T cells expressing OSM were also detected in giant papillae, as well as surface expression of OSMR beta in HconEpiCs. Recombinant human OSM strongly activated both STAT1 and STAT3 in HconEpiCs, inducing the expression of various tissue remodeling-related genes.