Affiliation:
1. Shanxi Key Laboratory of Stem Cells for Immunological Dermatosis Institute of Dermatology, Taiyuan Central Hospital of Shanxi Medical University Taiyuan China
2. Shanxi Key Laboratory of Stem Cells for Immunological Dermatosis Institute of Dermatology, Taiyuan City Central Hospital Taiyuan China
Abstract
AbstractObjectiveIncreased angiogenesis is a pathological feature of psoriasis, but the pathomechanisms of angiogenesis in psoriasis are not clear. Interleukin‐17A (IL‐17A) is the major effect factor in the pathogenesis of psoriasis. Our results showed that IL‐17A can promote angiogenesis and cause endothelial cell inflammation. Autophagy plays an important role not only in regulating inflammation, but also in regulating angiogenesis. Whether angiogenesis in psoriasis is related to autophagy remains unclear. In this study, we treated human umbilical vein endothelial cells (HUVECs) with IL‐17A to simulate increased angiogenesis to study whether increased angiogenesis in psoriasis is related to autophagy.Methods and ResultsOur results showed that treatment of HUVECs with IL‐17A significantly increased angiogenesis and expression levels of mRNA for multiple proinflammatory cytokines (CCL20, IL‐8, CCL2, IL‐6, and IL‐1β) and, while decreasing intracellular levels of nitric oxide (NO) and NO synthase (NOS) activity. Moreover, IL‐17A inhibited autophagy as shown that IL‐17A significantly increased expression levels of LC3II and p62 proteins. Induction of autophagy ameliorated IL‐17A‐mediated inflammatory response and inhibited angiogenesis, accompanied by increased p‐AMPKα(Thr172) and p‐ULK1(Ser555) expression, and decreased p‐mTOR(Ser2448) and p‐ULK1(Ser757) expression. Furthermore, inhibition of either AMPK or lysosomal acidification completely overrode autophagy‐induced changes in angiogenesis and NOS activity. Finally, induction of autophagy decreased apoptosis and caspase‐3 activity in IL‐17A‐treated HUVECs.ConclusionsThese results showed that IL‐17A is involved in angiogenesis and inflammatory response by inhibiting autophagy through AMPK signaling pathway, suggesting that autophagy may be a new therapeutic target for psoriasis.
Funder
National Natural Science Foundation of China
Cited by
2 articles.
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