Upregulated E3 ligase tripartite motif‐containing protein 21 in psoriatic epidermis ubiquitylates nuclear factor‐κB p65 subunit and promotes inflammation in keratinocytes*

泛素连接酶 下调和上调 角质形成细胞 炎症 基因敲除 趋化因子 促炎细胞因子 免疫沉淀 细胞生物学 化学 分子生物学 癌症研究 生物 泛素 免疫学 体外 细胞凋亡 生物化学 抗体 基因
作者
Luting Yang,T. Zhang,Chen Zhang,Chunying Xiao,Xiaocui Bai,Gang Wang
出处
期刊:British Journal of Dermatology [Oxford University Press]
卷期号:184 (1): 111-122 被引量:62
标识
DOI:10.1111/bjd.19057
摘要

BACKGROUND: Tripartite motif-containing protein 21 (Trim21) is an E3 ubiquitin-protein ligase that plays pivotal roles in various diseases. However, its role in mediating keratinocyte inflammation, which is a hallmark of psoriasis, has not been thoroughly elucidated. OBJECTIVES: To clarify whether Trim21 plays a pivotal role in regulating keratinocyte inflammation in psoriasis, while focusing on identifying key Trim21 substrates involved in mediating proinflammatory cytokine and chemokine production. MATERIALS AND METHODS: Cytokine and chemokine secretion was examined by quantitative real-time polymerase chain reaction (qPCR) in Trim21-knockdown human keratinocytes. Downstream pathways and substrates of Trim21 were evaluated using immunoblotting, immunoprecipitation and immunofluorescence. The influence of Trim21 ubiquitination on its substrates was tested by in vitro ubiquitination assay, immunoprecipitation and immunofluorescence. The effectiveness of targeting Trim21 for psoriasis treatment was assessed in vivo with haematoxylin and eosin staining, immunofluorescence and qPCR. RESULTS: Knocking down Trim21 expression alleviated keratinocyte inflammation. Trim21 colocalized with p65/nuclear factor (NF)-κB in the cytosol and physically bound and ubiquitinated p65 via a lysine 63 (K63) linkage. Instead of changing p65 protein stability, Trim21 enhanced the interaction of p65 with IκB kinase, which promoted p65 phosphorylation, nuclear transport and downstream gene activation. Finally, both in vitro and in vivo experiments verified that topical application of Trim21-specific small interfering RNA markedly ameliorated imiquimod-induced psoriasis-like lesions. CONCLUSIONS: Our study confirms that upregulated Trim21 in psoriatic epidermis ubiquitylates p65 and activates the NF-κB pathway, which promotes keratinocyte inflammation. Hence, Trim21 represents a potential target for psoriasis treatment.
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