食品科学 ›› 2025, Vol. 46 ›› Issue (22): 157-170.doi: 10.7506/spkx1002-6630-20250509-038

• 基础研究 • 上一篇    下一篇

苦荞类外泌体纳米囊泡调控巨噬细胞RAW264.7炎症反应及极化的体外机制

曹亚楠,刘乙志,彭镰心   

  1. (1.成都大学食品与生物工程学院,农业农村部杂粮加工重点实验室,四川?成都 610106;2.四川省杂粮产业化工程技术研究中心,四川?成都 610106)
  • 发布日期:2025-11-21
  • 基金资助:
    四川省科技厅计划项目(2023ZYD0078);现代农业产业技术体系四川杂粮创新团队专项(SCCXTD-2024-20); 西南民族大学青藏高原民族药用资源保护与利用实验室开放基金项目(QTPEM2201)

Mechanism by Which Tartary Buckwheat-Derived Exosome-like Nanovesicles Regulate the Inflammatory Response and Polarization of RAW264.7 Cells in Vitro

CAO Yanan, LIU Yizhi, PENG Lianxin   

  1. (1. Key Laboratory of Coarse Cereal Processing, Ministry of Agriculture and Rural Affairs, School of Food and Biological Engineering, Chengdu University, Chengdu 610106, China;2. Sichuan Engineering & Technology Research Center of Coarse Cereal Industrialization, Chengdu 610106, China)
  • Published:2025-11-21

摘要: 目的:探究苦荞来源类外泌体纳米囊泡(tartary buckwheat-derived exosome-like nanovesicles,TELN)对脂多糖(lipopolysaccharide,LPS)诱导的巨噬细胞RAW264.7炎症反应及极化的调控作用与机制。方法:首先采用尺寸排阻色谱(size exclusion chromatography,SEC)法从苦荞中提取TELN,并进行表征与鉴定;然后以巨噬细胞RAW264.7为研究模型,通过转录组学分析LPS处理组与LPS+TELN共处理组中巨噬细胞RAW264.7的基因表达差异;通过酶联免疫吸附测定(enzyme-linked immunosorbent assay,ELISA)法检测关键炎症因子白细胞介素(interleukin,IL)-6、肿瘤坏死因子α(tumor necrosis factor-α,TNF-α)、IL-1β、IL-10分泌水平;利用实时定量荧光聚合酶链式反应(quantitative polymerase chain reaction,qPCR)检测炎症因子mRNA表达水平;同时采用流式细胞术和Western blot分析TELN对LPS刺激下巨噬细胞RAW264.7极化的影响,初步探究TELN在调控炎症中的作用和机制。结果:采用SEC法提取的TELN粒径分布均匀,其平均粒径为145.8 nm,浓度为(1.305±0.074)×1010 particles/mL;转录组分析结果显示,TELN作用下巨噬细胞衍生趋化因子、泛素化、磷酸化蛋白等显著上调,同时S100A8等调节免疫和炎症的基因表达水平也明显增加。ELISA结果显示,TELN处理组细胞上清液中促炎因子IL-6、TNF-α和IL-1β水平分别下降(75.6±0.9)%(P<0.000 1)、(10.9±0.2)%(P<0.000 1)和(57.8±6.8)%(P<0.000 1),同时抗炎因子IL-10水平上升(69.7±4.6)%(P<0.000 1);qPCR结果在转录水平证实TELN显著下调IL-6、TNF-α和IL-1β mRNA表达,上调IL-10 mRNA表达。流式细胞术与Western blot分析结果一致表明,TELN能够显著抑制LPS诱导的M1型极化标志物CD86的表达,但未检测到CD206蛋白表达,提示TELN未促进M2型极化。结论:TELN通过双向调控炎症因子分泌(有效抑制促炎因子IL-6、TNF-α、IL-1β释放,显著提升抗炎因子IL-10水平)和抑制巨噬细胞向M1型极化,从而发挥抗炎作用。其对IL-6表达的抑制效果尤为突出,提示其作用可能与靶向核因子κB等信号通路有关。本研究可为深入解析苦荞的营养与免疫调节机制提供新视角。

关键词: 苦荞来源类外泌体纳米囊泡;巨噬细胞RAW264.7;转录组学;生物信息学;炎症

Abstract: Objective: To investigate the regulatory effect and underlying mechanism of tartary buckwheat-derived exosome-like nanovesicles (TELN) on lipopolysaccharide (LPS)-induced inflammatory response and polarization in murine macrophage RAW264.7 cells. Methods: TELN were extracted from tartary buckwheat using size-exclusion chromatography and characterized. RAW264.7 macrophages were divided into a control, an LPS-treated group, and an LPS + TELN-treated group. Transcriptomic analysis was performed to identify the differences in gene expression between these groups. The secretion levels of the key inflammatory cytokines interleukin (IL)-6, tumor necrosis factor-α (TNF-α), IL-1β, and IL-10 in cell culture supernatants were measured by enzyme-linked immunosorbent assay (ELISA). The mRNA expression of these cytokines was detected by real-time quantitative polymerase chain reaction (qPCR). The impact of TELN on LPS-induced macrophage polarization was analyzed using flow cytometry and Western blot. Results: TELN exhibited a homogeneous size distribution with an average diameter of 145.8 nm and a concentration of (1.305 ± 0.074) × 1010 particles/mL. The transcriptomic analysis revealed significant upregulation of the genes encoding macrophage-derived chemotactic factors, ubiquitinated proteins, phosphorylated proteins, and immune/inflammatory regulators (e.g., S100A8) in the TELN-treated group. The ELISA results demonstrated that compared with the LPS group, TELN significantly reduced the levels of the pro-inflammatory cytokines IL-6, TNF-α, and IL-1β in supernatants by (75.6 ± 0.9)% (P < 0.000 1), (10.9 ± 0.2)% (P < 0.000 1), and (57.8 ± 6.8)% (P < 0.000 1), respectively, while elevating the anti-inflammatory cytokine IL-10 by (69.7 ± 4.6)% (P < 0.000 1). The qPCR results confirmed that TELN significantly downregulated the mRNA expression of IL-6, TNF-α, and IL-1β and upregulated IL-10 mRNA expression at the transcriptional level. Flow cytometry and Western blot analyses consistently showed that TELN significantly suppressed the LPS-induced expression of the M1 polarization marker CD86. However, no detectable CD206 protein expression was observed, indicating that TELN did not promote M2 polarization. Conclusion: TELN exerts an anti-inflammatory effect by bidirectionally modulating cytokine secretion (effectively inhibiting the release of the pro-inflammatory cytokines IL-6, TNF-α, and IL-1β while significantly enhancing the level of anti-inflammatory IL-10) and suppressing M1 macrophage polarization. Particularly, TELN has a pronounced inhibitory effect on IL-6 expression, suggesting that its mechanism of action may be related to targeting signal pathways such as nuclear factor kappa-B (NF-κB). This study provides novel insights into the nutritional and immunomodulatory mechanisms of tartary buckwheat.

Key words: tartary buckwheat-derived exosome-like nanovesicles; RAW264.7 macrophages; transcriptomics; bioinformatics; inflammation

中图分类号: