口腔医学 ›› 2026, Vol. 46 ›› Issue (7): 504-513.doi: 10.13591/j.cnki.kqyx.2026.07.004

• 基础与临床研究 • 上一篇    下一篇

大肠杆菌外膜囊泡负载硫化亚铁对口腔鳞状细胞癌的抗肿瘤效应

李昂1, 郭舒琪1, 孟箭1,2(), 单学龙1, 刘珍1, 朱升辉1   

  1. 1 徐州医科大学徐州临床学院, 江苏徐州 (221009)
    2 徐州市中心医院口腔科, 江苏徐州 (221009)
  • 收稿日期:2025-09-11 出版日期:2026-07-28 发布日期:2026-07-23
  • 通讯作者: 孟 箭 E-mail:mrocket@126.com
  • 基金资助:
    江苏省老年健康科研项目(LKM2024031)

Antitumor effects of Escherichia coli-derived outer membrane vesicles loaded with ferrous sulfide on oral squamous cell carcinoma

LI Ang1, GUO Shuqi1, MENG Jian1,2(), SHAN Xuelong1, LIU Zhen1, ZHU Shenghui1   

  1. 1 Xuzhou Clinical College, Xuzhou Medical University, Xuzhou 221009, China
  • Received:2025-09-11 Online:2026-07-28 Published:2026-07-23

摘要:

目的 研究大肠杆菌外膜囊泡(OMV)负载硫化亚铁(FeS)形成的复合物OMV@FeS对口腔鳞状细胞癌(oral squamous cell carcinoma,OSCC)的疗效。方法 使用超高速离心法提取大肠杆菌OMV,并与FeS复合制得OMV@FeS;对OMV@FeS的微观形态、平均粒径及Zeta电位、元素构成进行表征;并对OMV@FeS在808 nm激光照射下的光热性能进行考察。构建SCC-7细胞小鼠皮下移植瘤模型,采用DCFH-DA探针和JC-1探针分别检测胞内活性氧自由基(reactive oxygen species,ROS)水平,以及线粒体膜电位变化;并通过CCK-8和Calcein-AM/PI双染色评价OMV@FeS联合激光治疗对SCC-7细胞的协同杀伤效应;采用流式细胞术评价OMV@FeS及联合激光治疗对肿瘤相关巨噬细胞极化的促进作用及促进未分化树突状细胞成熟的作用。建立SCC-7细胞小鼠皮下移植瘤模型,系统评估OMV@FeS在体抗肿瘤疗效及其生物安全性。结果 透射电子显微镜(transmission electron microscope,TEM)分析证实,FeS均匀分布于OMV囊泡内形成OMV@FeS复合物;在近红外激光(808 nm)照射下,OMV@FeS(>100 μg/mL)体系温度可升温至55 ℃以上,满足光热治疗所需的肿瘤消融温度,光热转换率为58.7%,具有良好的光热性能及光热稳定性。OMV@FeS辅助激光照射后,可于SCC-7细胞内生成大量ROS,并JC-1荧光标记的线粒体膜电位显著下降;Calcein-AM/PI活/死细胞双染及CCK-8结果表明OMV@FeS联合近红外激光对SCC-7细胞具有明显的协同杀伤作用。CD86和CD206流式细胞术结果表明OMV@FeS能有效诱导M2型巨噬细胞转型为M1型。CD80和CD86流式细胞分析证实OMV@FeS联合近红外激光可有效促进树突状细胞成熟。OMV@FeS联合激光干预表现出更为明显的抑瘤效果,SCC-7细胞小鼠皮下移植瘤体积持续缩小。HE染色结果显示,肿瘤细胞出现明显的凋亡或坏死特征,进一步验证了该联合治疗策略在体内具有良好的抗肿瘤效应。结论 OMV@FeS复合物在近红外激光照射下可发挥光热治疗、光动力学治疗与免疫治疗的协同作用,实现了物理治疗与生物免疫治疗的联合增效,对OSCC具有积极的治疗作用。

关键词: 口腔鳞状细胞癌, 大肠杆菌外膜囊泡, 硫化亚铁, 光热治疗, 免疫治疗

Abstract:

Objective To evaluate the therapeutic efficacy of OMV@FeS against oral squamous cell carcinoma(OSCC). Methods Escherichia coli-derived outer membrane vesicle (OMV) was extracted using ultracentrifugation and co-precipitated with FeS to form OMV@FeS. The morphology, average particle size, Zeta potential, and elemental composition of OMV@FeS were characterized. Photothermal performance under 808 nm laser irradiation was assessed. Intracellular reactive oxygen species(ROS) levels and mitochondrial membrane potential changes were detected using DCFH-DA and JC-1 probes respectively on squamous cell carcinoma(SCC-7) cells. The synergistic cytotoxicity of OMV@FeS combined with laser irradiation was evaluated through CCK-8 and Calcein-AM/PI dual staining, respectively. Flow cytometry analysis was employed to evaluate the induction of tumor-associated macrophage polarization and maturation of undifferentiated dendritic cells. A subcutaneous xenograft model of SCC-7 was developed to systematically evaluate the antitumor efficacy and biosafety of OMV@FeS. Results Transmission electron microscopy(TEM) analysis confirmed that FeS was uniformly distributed within OMV vesicles to form OMV@FeS. Under near-infrared laser (808 nm) irradiation, the temperature of the OMV@FeS system (>100 μg/mL) could exceed 55 ℃, meeting the tumor ablation temperature required for photothermal therapy. The photothermal conversion rate was 58.7%, demonstrating excellent photothermal performance and stability. When combined with OMV@FeS under laser irradiation, significant ROS generation and a marked decrease in JC-1 fluorescence-labeled mitochondrial membrane potential were observed within SCC-7 cells. Calcein-AM/PI dual staining and CCK-8 assays revealed that the combination of OMV@FeS with a near-infrared laser exhibited significant synergistic cytotoxic effects against SCC-7 cells. Flow cytometry analysis demonstrated that OMV@FeS effectively induced the polarization of M2 macrophages toward the M1 phenotype. Furthermore, flow cytometry analysis of CD80 and CD86 demonstrated that OMV@FeS combined with near-infrared laser irradiation significantly promoted the maturation of dendritic cells. The tumor-inhibiting effect of OMV@FeS under laser intervention was highly significant in SCC-7 tumor-bearing mice, as evidenced by a continuous reduction in tumor volume. HE staining demonstrated significant apoptotic or necrotic features in tumor cells, further validating the efficacy of this combined therapy strategy in vivo. Conclusion OMV@FeS exhibits synergistic effects of photothermal therapy, photodynamic therapy and immunotherapy under near-infrared laser irradiation, realizing combined enhancement of physical therapy and biological immunotherapy, thereby exerting a positive therapeutic effect on OSCC.

Key words: oral squamous cell carcinoma, Escherichia coli derived-outer membrane vesicles, iron sulfide, photothermal therapy, immunotherapy

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