Li Kejun,Du Liqing,Liu Qiang,Song Huijuan.Effects of glycosylated nanoparticles on radiation-induced the polarization of macrophages in early injured lung tissue[J].Chinese Journal of Radiological Medicine and Protection,2023,43(11):858-865
Effects of glycosylated nanoparticles on radiation-induced the polarization of macrophages in early injured lung tissue
Received:February 20, 2023  
DOI:10.3760/cma.j.cn112271-20230220-00172
KeyWords:Radiation-induced lung injury  Pulmonary macrophages  M2 polarization  Reactive oxygen species  Inflammation
FundProject:国家自然科学基金(82001954,32071241,81972976,32171239);辐射防护实验室开放基金(CIRP-DTRI20220202);中国医学科学院医疗健康科技创新项目(2022-I2M-2-003)
Author NameAffiliationE-mail
Li Kejun Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300192, China  
Du Liqing Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300192, China  
Liu Qiang Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300192, China  
Song Huijuan Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300192, China songhuijuan@irm-cams.ac.cn 
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Abstract::
      Objective To explore the effects of glycosylated nanoparticles on early radiation responses including the generation of reactive oxygen species (ROS), the polarization of pulmonary macrophages, and secretion of inflammatory cytokines in mice lung tissues.Methods Twenty mice were randomly divided into control group, drug administration group, irradiation group and irradiation + drug administration group. The irradiation group and irradiation + drug administration group were subjected to whole lung irradiation with X-rays. The antioxidant ability of glycosylated nanoparticles was characterized using ROS indicator (CM-H2DCFDA). The M2 polarization of pulmonary macrophages was detected by flow cytometry and PCR. The mRNA and protein expression levels of inflammatory cytokines were investigated by PCR and ELISA assay, respectively.Results Compared with the irradiation group, the intensity of ROS fluorescence signals was significantly lower (t=15.76, P < 0.05), the proportion of M2-type macrophages was significantly higher (t=2.89, P < 0.05), the expression level of arginase 1 (ARG-1) gene was elevated, and the expression levels of tumour necrosis factor α (TNF-α), interleukin 1β (IL-1β) and interleukin 6 (IL-6) inflammatory factors were significantly reduced (t=3.32, 2.90, 2.85, 4.55, 2.88, P < 0.05) in the lung tissues of irradiation + treatment group.Conclusions Glycosylated nanoparticles can effectively scavenge ROS, trigger polarization of M2 macrophage, dampen inflammatory responses, and thus potentially alleviate radiation-induced lung injury.
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