基础医学与临床 ›› 2023, Vol. 43 ›› Issue (1): 110-115.doi: 10.16352/j.issn.1001-6325.2023.01.0110

• 研究论文 • 上一篇    下一篇

鲍曼不动杆菌外膜囊泡诱发人单核-巨噬细胞THP-1的炎性反应

付士祥1, 席月2, 丁龙坤2, 闫曼2, 赵俊1, 焦玉东1, 吴亮2*   

  1. 1.扬州市第三人民医院,江苏 扬州 225000;
    2.江苏大学 医学院, 江苏 镇江 212013
  • 收稿日期:2021-08-26 修回日期:2022-06-02 出版日期:2023-01-05 发布日期:2022-12-27
  • 通讯作者: *wl_ujs@163.com
  • 基金资助:
    扬州市2020年市级社会发展计划(YZ2020108)

Acinetobacter baumannii outer membrane vesicles induced inflammation of human monocyte-derived macrophages THP-1

FU Shixiang1, XI Yue2, DING Longkun2, YAN Man2, ZHAO Jun1, JIAO Yudong1, WU Liang2*   

  1. 1. The Third People’s Hospital of Yangzhou, Yangzhou 225000;
    2. School of Medicine, Jiangsu Uiversity, Zhenjiang 212013, China
  • Received:2021-08-26 Revised:2022-06-02 Online:2023-01-05 Published:2022-12-27
  • Contact: *wl_ujs@163.com

摘要: 目的 建立超速离心法纯化鲍曼不动杆菌外膜囊泡(OMVs),并探讨OMVs诱发人单核-巨噬细胞THP-1炎性反应能力。方法 大量培养鲍曼不动杆菌标准菌株,从培养液上清中以超速离心法提纯OMVs并以透射电镜观察形态。分别以5 和50 μg/mL的OMVs与THP-1细胞共培养,RT-qPCR检测NOD样受体家族蛋白(NLRP3)和caspase-1表达量;ELISA检测培养液上清中IL-1β含量;蛋白质印迹法检测细胞自噬相关蛋白LC-3Ⅱ和Beclin-1表达量;酶促动力学法检测细胞caspase-3酶活性;流式细胞测量术检测细胞活性氧表达量。结果 成功提纯鲍曼不动杆菌OMVs。OMVs可以诱导THP-1细胞NLRP3炎性复合体活化,并增加自噬相关蛋白LC-3Ⅱ和Beclin-1表达量(P<0.05),以及上调凋亡关键因子caspase-3酶活性(P<0.05)。共培养1 h时,OMVs可以显著上调THP-1细胞活性氧表达(P<0.05)。结论 鲍曼不动杆菌OMVs可以显著活化巨噬细胞NLRP3炎性复合体。

关键词: 鲍曼不动杆菌, 外膜囊泡, 炎性反应, 自噬, 凋亡

Abstract: Objective To establish an ultra-filtration centrifugation method to purify the outer membrane vesicles (OMVs) of Acinetobacter baumannii(A.baumannii), and to investigate the ability of OMVs to induce inflamma-tion in human monocyte-derired macrophages THP-1. Methods A.baumannii was cultured, and the OMVs were purified from the supernatant of culture medium by ultra-filtration centrifuge,the morphology was observed by transmission electron microscopy. THP-1 cells were incubated with OMVs at the concentration of 5 and 50 μg/mL respectively. The expression of NOD-like receptor protein 3(NLRP3) and caspase-1 were determined by RT-qPCR. The concentration of IL-1β in culture medium supernatant was measured by ELISA. The expression of LC-3Ⅱ and Beclin-1 was examined by Western blot. The activity of caspase-3 was determined by enzyme dynamics assay. The expression of reactive oxygen species (ROS) was determined by flow cytometry. Results A.baumannii OMVs was purified successfully. The OMVs could activate NLRP3 inflammasome, increase the expression of LC-3Ⅱ and Beclin-1 and up-regulate the activity of caspase-3 (P<0.05). The OMVs significantly up-regulated the expression of ROS in THP-1 cells after 1 h co-culture (P<0.05). Conclusions OMVs of A.baumannii can significantly activate macrophages NLRP3 inflammasome and induce cell autophagy and apoptosis.

Key words: Acinetobacter baumannii, outer membrane vesicles, inflammation, autophagy, apoptosis

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