首页|期刊导航|空军军医大学学报|鲍曼不动杆菌对RAW264.7巨噬细胞的损伤效应及Siglec-G的调控作用

鲍曼不动杆菌对RAW264.7巨噬细胞的损伤效应及Siglec-G的调控作用OACHSSCD

Damaging effects of Acinetobacter baumannii on RAW264.7 macrophages and the regulatory role of Siglec-G

中文摘要英文摘要

目的 研究鲍曼不动杆菌(A.baumannii)对小鼠巨噬细胞的损伤作用及Siglec-G的调控作用,并分析其肺炎模型的特征.方法 将RAW264.7细胞与A.baumannii共培养,检测细胞存活率及炎症因子水平;用siRNA干扰Siglec-G表达后观察炎症因子变化.通过气管滴注建立小鼠肺炎模型,观察肺病理、肺泡灌洗液(BALF)炎症因子、蛋白含量、细胞计数和肺湿/干质量比.结果 A.baumannii以时间-剂量依赖方式诱导RAW264.7细胞死亡,并使细胞上清液TNF-α、IL-6显著升高.干扰Siglec-G表达后,细菌诱导的IL-6分泌被显著抑制,TNF-α水平未受影响.而在未感染状态下,敲低Siglec-G可降低TNF-α的基础表达水平.在体内,感染24 h后小鼠肺部出现显著炎症,BALF中炎症因子、蛋白和细胞总数均升高,但肺湿/干质量比无显著变化.结论 A.baumannii可直接损伤巨噬细胞并诱发炎症反应,Siglec-G选择性调控IL-6的产生.小鼠肺炎模型表现为快速进展的炎症而非严重肺水肿.

Objective To investigate the damaging effects of Acinetobacter baumannii(A.baumannii)on mouse macrophages and the regulatory role of Siglec-G,and to analyze the characteristics of its pneumonia model.Methods RAW264.7 cells were co-cultured with A.baumannii to assess cell viability and inflammatory cytokine levels;changes in inflammatory cytokines were observed following siRNA-mediated inhibition of Siglec-G expression.A mouse pneumonia model was established via tracheal instillation to evaluate lung pathology,inflammatory cytokines,proteins,and cell counts in bronchoalveolar lavage fluid(BALF),as well as the wet-to-dry lung weight ratio.Results A.baumannii induced RAW264.7 cell death in a time-and dose-dependent manner and markedly elevated the levels of TNF-α and IL-6 in the cell supernatant.Knockdown of Siglec-G markedly decreased the secretion of IL-6 induced by bacteria,while it had no obvious effect on TNF-α production.In the absence of infection,knocking down Siglec-G reduced the basal expression level of TNF-α.In vivo,significant inflammation was observed in the lungs of mice 24 h after infection,with elevated levels of inflammatory cytokines,proteins,and total cell counts in BALF;however,the wet-to-dry lung weight ratio did not change significantly.Conclusion A.baumannii can directly damage macrophages and induce an inflammatory response,while Siglec-G selectively regulates IL-6 production.The mouse pneumonia model exhibits rapidly progressing inflammation rather than severe pulmonary edema.

许映斐;李玉娟;高永恒;潘蕾

空军军医大学唐都医院呼吸与危重症医学科,陕西西安 710038||解放军联勤保障部队第九二八医院呼吸与重症医学科,海南海口 570100空军军医大学唐都医院呼吸与危重症医学科,陕西西安 710038空军军医大学唐都医院呼吸与危重症医学科,陕西西安 710038空军军医大学唐都医院呼吸与危重症医学科,陕西西安 710038

医药卫生

鲍曼不动杆菌巨噬细胞Siglec-G炎症肺炎RAW264.7细胞炎症因子TNF-α

Acinetobacter baumanniimacrophagesSiglec-GinflammationpneumoniaRAW264.7 cellsinflammatory cytokinesTNF-α

《空军军医大学学报》 2026 (8)

1100-1105,6

陕西省重点研发计划项目(2024SF-YBXM-092)

10.13276/j.issn.2097-1656.2026.08.002

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