Longpeng Ma, Xiangqian Luo, Lihua Mo, Jialiang Fan, Dabo Liu
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引用次数: 0
Abstract
Objective:To prepare PLGA nanoparticles loaded with Der f 1/IGF-1(Der f 1/IGF-1 NPs) and investigate their role in promoting the formation of Treg cells. Methods:NPs coated with Der f 1/IGF-1 were prepared by double emulsion method and their physicochemical properties and cumulative release rate in vitro were analyzed. After pretreatment, BMDC was divided into Saline group, Blank NPs group, Der f 1/IGF-1 group and Der f 1/IGF-1 NPs group. Determination of the expression of IL-10 and TGF-β in BMDC by ELISA. The number of Treg cells was detected by flow cytometry. Results:The results showed that Der f 1/IGF-1 NPs were spherical structures, with good dispersion, particle size less than 200 nm, negative charge and stable slow-release effect of Zeta potential. After BMDC pretreatment, the expression levels of TGF-β and IL-10 in BMDC cells in the Der f 1/IGF-1 NPs group were significantly increased compared with the Blank NPs group, and the difference was statistically significant(P<0.001). After co-culture with CD4+ T cells, the proportion of Treg cells produced in the Der f 1/IGF-1 NPs group was significantly increased, and the difference was statistically significant(P<0.001). Conclusion:Der f 1/IGF-1 NPs can induce Treg cell generation in vitro. This study provides a new and more effective method for the reconstruction of immune tolerance dysfunction.
目的:制备负载Der f 1/IGF-1的PLGA纳米粒子(Der f 1/IGF-1 NPs),并研究其在促进Treg细胞形成中的作用。方法:采用双乳液法制备Der f1/IGF-1包被的纳米颗粒,并对其理化性质和体外累积释放率进行分析。预处理后,将BMDC分为生理盐水组、空白NPs组、Der f1/IGF-1组和Der f1-IGF-1 NPs组。ELISA法检测白细胞介素-10和转化生长因子-β在骨髓基质干细胞中的表达。流式细胞仪检测Treg细胞的数量。结果:Der f 1/IGF-1纳米粒子为球形结构,具有良好的分散性,粒径小于200nm,带负电荷,Zeta电位具有稳定的缓释效果。Der f 1/IGF-1 NPs组BMDC细胞中TGF-β和IL-10的表达水平较空白NPs组显著升高,结论:Der f 1/IGF-1 NPs在体外可诱导Treg细胞生成,为免疫耐受功能障碍的重建提供了一种新的、更有效的方法。