Role of IL-23/IL-17 inflammatory axis in the pathogenesis of psoriasis-like lesions induced by imiquimod in mice

作者
Ping Li
出处
期刊:Chinese Journal of Pathophysiology
摘要

AIM:To observe the dynamic changes of IL-23/IL-17 inflammatory axis in psoriasis-like lesions of mice induced by imiquimod(IMQ).METHODS: BALB/c female mice were randomly divided into control group and IMQ group.The morphological changes of lesional skin in mice were evaluated according to the psoriasis area and severity index(PASI) and HE staining.cytokine antibody chips were used to determine the cytokine changes in serum and lesions.The mRNA and protein expression of cytokines were analyzed by cytometric bead array,real-time PCR and Western blotting.Moreover,the changes of cellular constituents in the peripheral blood and splenic cells of mice were detected by flow cytometry.RESULTS: Typical psoriasis-like skin lesions,such as red scaly skin plaques,caused by topical IMQ showed a parabolic dynamic change.There was a dynamic increase in proinflammatory cytokines of the IL-23/IL-17 axis in IMQ-treated skin.IMQ application resulted in elevated expression of cytokines related with IL-23/IL-17 inflammatory axis,Th1-type cytokines,Th2-type cytokines and Treg-type cytokines at day 4.IMQ-treated BALB/c mice showed an increased pericentage of dentric cells in peripheral blood and spleen compared with control animals.Percentages of Th17 and Treg in IMQ-treated mice were increased by 3~4 times and twice as compared with control mice,respectively.CONCLUSION: The skin lesions,histopathological features and cytokine changes in mice induced by IMQ are similar to human psoriasis,which are suitable for investigating the pathogenesis of psoriasis as a psoriasis-like model.IL-23/IL-17 axis is involved in the formation of psoriasis-like skin lesions in mice induced by IMQ and presents a dynamic change.Besides,Th1 cell-mediated inflammatory response is also activated in the formation of lesional skin,accompanied by the increase expression of Th2 and Treg cytokines in a feedback mechanism.

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