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. 2024 Jun 20;17:4001–4016. doi: 10.2147/JIR.S474879

Figure 3.

Figure 3

In vivo effects of IL-36, IL-37 and IL-38 on OA development. Injection of IL-36Ra inhibited Tgfbr2−/− spontaneous OA mice synovitis, whereas injection of IL-36α promoted OA development. In DMM-induced OA mice, injection of IL-36Ra or IL-36Ra@Gel suppressed severity of cartilage tissue destruction. On the contrary, injection of IL-36α exacerbated OA progress. For IL-37, injection of IL-37 into TMJOA rats suppressed swelling and hyperplasia in tissues around the cartilage. Regarding role of IL-38, DMM-induced OA mice injected with overexpressed IL-38 significantly improved cartilage damage, downregulated OARSI score.

Abbreviations: OA, osteoarthritis; DMM, destabilization of the medial meniscus; IL-36Ra@Gel, poly(lactic-co-glycolic acid)-poly(ethyleneglycol)-poly(lactic-co-glycolic acid) (PLGA-PEG-PLGA) hydrogel system incorporating IL-36Ra; TMJOA, temporomandibular joint OA; OARSI, Osteoarthritis Research Society International.