甘露糖受体通过MAPK和NF-κB途径靶向杜柏多糖PLGA纳米颗粒,增强bmdc的免疫活性。

IF 5.6 2区 医学 Q1 BIOPHYSICS
Xin Hu, Jia Meng, Yi Liao, Yanwen Yang, Yao Wang, Zhenhui Song, Ziwei Liu, Haibo Feng
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引用次数: 0

摘要

研究了一种包裹杜仲多糖(EOPP)的甘露糖基聚乳酸-羟基乙酸(PLGA)纳米颗粒作为靶向免疫调节递送系统。体外实验证实,EOPP对脾脏淋巴细胞具有较低的细胞毒性,但显著增加脾脏淋巴细胞的增殖和细胞因子(IL-6和IFN-γ)的分泌。当与卵清蛋白(MN-EOPP/OVA)共递送时,该系统进一步增强免疫细胞分泌TNF-α、IL-12、IL-6和IFN-γ,并诱导骨髓源性树突状细胞(bmdc)的细胞骨架重塑和成熟。转录组学分析显示免疫相关基因显著上调,KEGG和PPI分析确定了关键信号通路的激活,包括MAPK (ERK, p38, JNK)和NF-κB。这些途径驱动抗原加工和树突状细胞功能相关基因的表达。总的来说,MN-EOPP/OVA通过抗原和免疫增强剂的协同递送有效地增强了体液和细胞免疫应答,支持其作为下一代疫苗佐剂策略的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mannose receptor targeted PLGA nanoparticles ofEucommia ulmoidespolysaccharide through the MAPK and NF-κB pathway to enhance the immune activity of BMDCs.

Mannosylated poly(lactic-co-glycolic acid) (PLGA) nanoparticles encapsulating Eucommia ulmoides polysaccharides (EOPP) were developed as a targeted immunomodulatory delivery system. In vitro evaluations confirmed that EOPP exhibited low cytotoxicity toward spleen lymphocytes while significantly increasing their proliferation and cytokine secretion (IL-6 and IFN-γ). When co-delivered with ovalbumin (MN-EOPP/OVA), the system further enhanced the secretion of TNF-α, IL-12, IL-6, and IFN-γ by immune cells and induced cytoskeletal remodeling and maturation in bone marrow-derived dendritic cells (BMDCs). Transcriptomic profiling revealed significant upregulation of immune-related genes, with KEGG and PPI analyses identifying activation of key signaling pathways, including MAPK (ERK, p38, JNK) and NF-κB. These pathways drive the expression of genes involved in antigen processing and dendritic cell function. Overall, MN-EOPP/OVA effectively enhanced both humoral and cellular immune responses by synergistic delivery of antigen and immunopotentiator, supporting its potential as a next-generation vaccine adjuvant strategy.

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来源期刊
Colloids and Surfaces B: Biointerfaces
Colloids and Surfaces B: Biointerfaces 生物-材料科学:生物材料
CiteScore
11.10
自引率
3.40%
发文量
730
审稿时长
42 days
期刊介绍: Colloids and Surfaces B: Biointerfaces is an international journal devoted to fundamental and applied research on colloid and interfacial phenomena in relation to systems of biological origin, having particular relevance to the medical, pharmaceutical, biotechnological, food and cosmetic fields. Submissions that: (1) deal solely with biological phenomena and do not describe the physico-chemical or colloid-chemical background and/or mechanism of the phenomena, and (2) deal solely with colloid/interfacial phenomena and do not have appropriate biological content or relevance, are outside the scope of the journal and will not be considered for publication. The journal publishes regular research papers, reviews, short communications and invited perspective articles, called BioInterface Perspectives. The BioInterface Perspective provide researchers the opportunity to review their own work, as well as provide insight into the work of others that inspired and influenced the author. Regular articles should have a maximum total length of 6,000 words. In addition, a (combined) maximum of 8 normal-sized figures and/or tables is allowed (so for instance 3 tables and 5 figures). For multiple-panel figures each set of two panels equates to one figure. Short communications should not exceed half of the above. It is required to give on the article cover page a short statistical summary of the article listing the total number of words and tables/figures.
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