Upregulated SKP2 Empowers Epidermal Proliferation Through Downregulation of P27 Kip1.

Lipeng Tang, Bowen Zhang, Guanzhuo Li, Xinmin Qiu, Zixin Dai, Hongying Liu, Ying Zhu, Bing Feng, Zuqing Su, Wenhui Han, Huilin Huang, Qiuping Li, Zihao Zhang, Maojie Wang, Huazhen Liu, Yuchao Chen, Yanmei Zhang, Dinghong Wu, Xirun Zheng, Taohua Liu, Jie Zhao, Chutian Li, Guangjuan Zheng
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Abstract

Background: Excessive growth of keratinocytes is the critical event in the etiology of psoriasis. However, the underlying molecular mechanism of psoriatic keratinocyte hyperproliferation is still unclear.

Objective: This study aimed to figure out the potential contributory role of S-phase kinase-associated protein 2 (SKP2) in promoting the hyperproliferation of keratinocytes in psoriasis.

Methods: We analyzed microarray data (GSE41662) to investigate the gene expression of SKP2 in psoriatic lesion skins compared with their adjacent non-lesional skin. Then, we further confirmed the mRNA and protein expression of SKP2 in human psoriatic skin tissues, imiquimod (IMQ)-induced psoriatic mice back skins and tumor necrosis factor α (TNF-α), interleukin (IL)-17A and IL-6-stimulated keratinocytes by using real-time quantitative polymerase chain reaction and western blot (WB). Furthermore, we explored the potential pathogenic role and its underlying cellular mechanism of SKP2 in promoting keratinocytes hyperproliferation through 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, cell cycle detection, 5-ethynyl-2'-deoxyuridine staining and WB. Finally, we determined whether inhibition of SKP2 can effectively alleviate the keratinocytes hyperproliferation in vivo.

Results: We identified that SKP2 is aberrantly upregulated in the psoriatic lesion skin and cytokines-stimulated keratinocytes. Moreover, upregulated SKP2 augments cytokines-induced keratinocytes hyperproliferation. Mechanistically, enhanced SKP2 increased the S phase ratio through inhibiting Cyclin-Dependent Kinase Inhibitor p27 (P27 Kip1) expression. Correspondingly, suppression of SKP2 with SMIP004 can significantly ease the epidermis hyperplasia in vivo.

Conclusion: Our results suggest that elevated SKP2 can empower keratinocytes proliferation and psoriasis-like epidermis hyperplasia via downregulation of P27 Kip1. Therefore, targeting SKP2-P27 Kip1 axis might be a promising therapeutic strategy for the treatment of psoriasis in future.

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上调的 SKP2 通过下调 P27 Kip1 促进表皮增殖
背景:角朊细胞过度增殖是银屑病病因中的关键事件。然而,银屑病角朊细胞过度增殖的分子机制尚不清楚:本研究旨在找出S期激酶相关蛋白2(SKP2)在促进银屑病角朊细胞过度增殖中的潜在作用:我们分析了微阵列数据(GSE41662),研究了银屑病皮损皮肤与邻近非皮损皮肤相比SKP2的基因表达。然后,我们通过实时定量聚合酶链反应和免疫印迹(WB)进一步证实了 SKP2 在人类银屑病皮肤组织、咪喹莫特(IMQ)诱导的银屑病小鼠背部皮肤以及肿瘤坏死因子α(TNF-α)、白细胞介素(IL)-17A 和 IL-6 刺激的角质形成细胞中的 mRNA 和蛋白表达。此外,我们还通过 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑试验、细胞周期检测、5-乙炔基-2'-脱氧尿苷染色和 WB,探讨了 SKP2 在促进角朊细胞过度增殖中的潜在致病作用及其细胞机制。最后,我们确定了抑制 SKP2 是否能有效缓解体内角朊细胞的过度增殖:结果:我们发现 SKP2 在银屑病皮损皮肤和细胞因子刺激的角朊细胞中异常上调。此外,上调的 SKP2 会增强细胞因子诱导的角质形成细胞过度增殖。从机理上讲,SKP2 的增强会通过抑制细胞周期蛋白依赖性激酶抑制剂 p27(P27 Kip1)的表达来提高 S 期比率。相应地,用SMIP004抑制SKP2可显著缓解体内表皮增生:我们的研究结果表明,SKP2 升高可通过下调 P27 Kip1 促进角质形成细胞增殖和银屑病样表皮增生。因此,靶向 SKP2-P27 Kip1 轴可能是未来治疗银屑病的一种有前景的治疗策略。
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