Potential roles of the IL-6 family in conjunctival fibrosis

• Published in: Experimental eye research 2021-09, Vol.210, p.108708-108708, Article 108708
• Main Authors: Watanabe-Kitamura, Fumika, Ogawa, Akiko, Fujimoto, Tomokazu, Iraha, Satoshi, Inoue-Mochita, Miyuki, Watanabe, Takahiro, Takahashi, Eri, Tanihara, Hidenobu, Inoue, Toshihiro
• Format: Article
• Language: English
• Subjects: Conjunctival fibroblast; Interleukin 6; Myofibroblast; Oncostatin
• ISSN: 0014-4835; 1096-0007
• DOI: 10.1016/j.exer.2021.108708

Elevated intraocular pressure (IOP) is a significant risk factor for vision loss due to glaucoma, which is a major cause of blindness worldwide. Glaucoma filtration surgery (GFS) is an important method to reduce IOP by guidance of aqueous humor into a newly built filtration bleb in the conjunctiva; management of the wound healing mechanism is essential for the success of GFS. Here, we investigated the roles of interleukin (IL)-6 family members during the wound healing process after GFS. At the surgical site, the expression levels of genes encoding IL-6, oncostatin M (OSM), their receptors, and collagen I were elevated at 3 h after GFS, whereas the levels of genes encoding transforming growth factor (TGF)-β, α-smooth muscle actin (SMA), type IV collagen, and fibronectin were elevated at 3 days after GFS. IL-6 trans-signaling and OSM signaling suppressed TGF-β-induced expression of α-SMA and collagen IV, as well as activation of the non-canonical TGF-β pathway, suggesting that IL-6 and OSM may aid in controlling the phase transition from inflammation to proliferation and remodeling. The suppressive effects of OSM were accompanied by STAT3 activation, such that STAT1 function was complementary to STAT3. Taken together, these observations indicated that IL-6 family members constitute early response genes after GFS, which can suppress TGF-β-induced expression of late response genes at the surgical site after GFS. •IL-6 family members constitute early response genes after trabeculectomy.•IL-6 family members can suppress TGF-β-induced expression of late response genes, such as α-SMA and type IV collagen, in cell culture.•The suppressive effects of IL-6 on the effects of TGF-β were accompanied by STAT3 activation, such that STAT1 function was complementary to STAT3.