[hPP10-Cu、Zn-SOD 融合蛋白的细胞膜穿透能力及其抗氧化和抗炎活性]。

Q3 Medicine
J Zhang, J Yao, Y Yang, F Wang, Q Zheng, X Li, C Liu
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引用次数: 0

摘要

目的研究携带人抗氧化蛋白铜锌超氧化物歧化酶(Cu, Zn-SOD)的人细胞膜穿透肽 hPP10 的细胞膜穿透能力,并评估这些融合蛋白的抗氧化和抗炎活性:方法:通过基因工程获得了融合蛋白 hPP10-Cu,Zn-SOD,并通过 Western 印迹进行了鉴定。方法:通过基因工程获得了融合蛋白 hPP10-Cu、Zn-SOD,并通过 Western 印迹进行了鉴定。融合蛋白的穿膜能力通过免疫荧光检测、荧光共聚焦检测和 Western 印迹进行了评估,其 SOD 酶活性通过商业试剂盒进行了检测,其对细胞活力的影响通过 MTT 检测进行了评估。在H2O2诱导氧化应激的HEK293细胞模型中,用流式细胞仪和RT-qPCR分析了hPP10-Cu、Zn-SOD对细胞凋亡的影响,用活性氧(ROS)检测评估了其抗氧化作用;在TPA诱导的小鼠耳部炎症模型中,用RT-qPCR、Western印迹和免疫组化检测了炎症因子的表达,评估了其抗炎作用:结果:成功获得了融合蛋白hPP10-Cu, Zn-SOD。免疫荧光检测证实,该融合蛋白在 HEK293 细胞中具有明显的膜穿透性,进入细胞后定位于细胞膜和细胞核中。在氧化应激细胞模型中,融合蛋白能明显抑制细胞凋亡,降低细胞内 ROS 水平;在小鼠耳部炎症模型中,融合蛋白能显著降低炎症因子的 mRNA 和蛋白表达:能够穿透细胞膜的融合蛋白hPP10-Cu, Zn-SOD具有很强的抗氧化和抗炎活性,且细胞毒性极低,这表明了hPP10作为一种高效载药载体的价值以及hPP10-Cu, Zn-SOD在护肤品开发中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Cell membrane-penetrating capacity of hPP10-Cu, Zn-SOD fusion protein and its antioxidant and anti-inflammatory activity].

Objective: To investigate the cell membrane-penetrating capacity of human cell-penetrating peptide hPP10 carrying human antioxidant protein Cu-Zn superoxide dismutase (Cu, Zn-SOD) and assess the antioxidant and anti-inflammatory activity of these fusion proteins.

Methods: The fusion protein hPP10-Cu, Zn-SOD was obtained by genetic engineering and identified by Western blotting. The membrane-penetrating ability of the fusion protein was evaluated by immunofluorescence assay, fluorescence colocalization assay and Western blotting, its SOD enzyme activity was detected using a commercial kit, and its effect on cell viability was assessed with MTT assay. In a HEK293 cell model of H2O2-induced oxidative stress, the effect of hPP10-Cu, Zn-SOD on cell apoptosis was analyzed with flow cytometry and RT-qPCR, and its antioxidant effect was assessed using reactive oxygen species (ROS) assay; its anti-inflammatory effect was evaluated in mouse model of TPA-induced ear inflammation by detecting expression of the inflammatory factors using RT-qPCR, Western blotting and immunohistochemistry.

Results: The fusion protein hPP10-Cu, Zn-SOD was successfully obtained. Immunofluorescence assay confirmed obvious membrane penetration of this fusion protein in HEK293 cells, localized both in the cell membrane and the cell nuclei after cell entry. hPP10-Cu, Zn-SOD at the concentration of 5 μmol/L exhibited strong antioxidant activity with minimal impact on cell viability at the concentration up to 10 μmol/L. The fusion protein obviously inhibited apoptosis and decreased intracellular ROS level in the oxidative stress cell model and significantly reduced mRNA and protein expression of the inflammatory factors in the mouse model of ear inflammation.

Conclusion: The fusion protein hPP10-Cu, Zn-SOD capable of penetrating the cell membrane possesses strong antioxidant and anti-inflammatory activities with only minimal cytotoxicity, demonstrating the value of hPP10 as an efficient drug delivery vector and the potential of hPP10-Cu, Zn-SOD in the development of skincare products.

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CiteScore
1.50
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