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硒纳米片在溃疡性结肠炎中的抗炎机制:蛋白质冠、GP130相互作用及转录组图谱

Anti-Inflammatory Mechanisms of Selenium Nanosheets in Ulcerative Colitis: Protein Corona, GP130 Interaction, and Transcriptomic Profile.

作者信息

Shen Dingyi, Gong Li, Yang Wei, Luo Jiaqi, Jin Zhen, Tang Youzhi

机构信息

Guangdong Laboratory for Lingnan Modern Agriculture, College of Veterinary Medicine, South China Agriculture University, Guangzhou, Guangdong, 510642, China.

Instrumental Analysis Research Center, Sun Yat-sen University, Guangzhou, Guangdong, 510275, China.

出版信息

Adv Sci (Weinh). 2025 Sep;12(36):e01832. doi: 10.1002/advs.202501832. Epub 2025 Jun 29.

Abstract

Ulcerative colitis (UC) is a complex inflammatory bowel disease characterized by multiple factors. Alleviating inflammation is the primary therapeutic approach. However, currently employed anti-inflammatory treatments have limited efficacy and cause side effects. Safer, more effective therapies are needed. Selenium nanosheets (SeNSs) are biocompatible, anti-inflammatory, and low-toxicity nanomaterials with high surface areas and abundant active sites, making them potential therapeutic agents for UC. This study indicates that SeNSs can interact with macrophages and adhere to their cell membranes, significantly increasing their internalization into cells. Proteomic analysis reveals that the main components of the SeNS protein corona are proteins involved in cell proliferation and migration, including those associated with the AKT/PI3K and NF-κB signaling pathways. SeNSs hydrophobically interact with GP130, inhibiting its expression. This interaction downregulates the proteins involved in the aforementioned pathways. In addition, a transcriptomic analysis confirms that SeNSs inhibit apoptosis, cytokine-cytokine receptor interactions, and the chemokine and TNF signaling pathways. In dextran sulfate sodium (DSS)-induced UC model mice, SeNSs significantly decrease IL-1β, IL-6, and TNF-α levels, alleviate tissue damage, and lower the disease activity index. These findings suggest that SeNSs can be a safe and effective treatment strategy for UC, offering a novel approach for managing inflammatory diseases.

摘要

溃疡性结肠炎(UC)是一种由多种因素导致的复杂炎症性肠病。减轻炎症是主要的治疗方法。然而,目前使用的抗炎治疗效果有限且会引发副作用。因此需要更安全、更有效的治疗方法。硒纳米片(SeNSs)是具有生物相容性、抗炎性且低毒性的纳米材料,其具有高表面积和丰富的活性位点,使其成为治疗UC的潜在药物。本研究表明,SeNSs可与巨噬细胞相互作用并黏附于其细胞膜,显著增加其内化进入细胞的能力。蛋白质组学分析显示,SeNS蛋白冠的主要成分是参与细胞增殖和迁移的蛋白质,包括与AKT/PI3K和NF-κB信号通路相关的蛋白质。SeNSs与GP130发生疏水相互作用,抑制其表达。这种相互作用下调了上述信号通路中涉及的蛋白质。此外,转录组学分析证实,SeNSs可抑制细胞凋亡、细胞因子-细胞因子受体相互作用以及趋化因子和TNF信号通路。在葡聚糖硫酸钠(DSS)诱导的UC模型小鼠中,SeNSs可显著降低IL-1β、IL-6和TNF-α水平,减轻组织损伤,并降低疾病活动指数。这些研究结果表明,SeNSs可能是一种治疗UC的安全有效的策略,为炎症性疾病的治疗提供了一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7194/12462919/beeb4b793544/ADVS-12-e01832-g008.jpg

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