首页|期刊导航|军事医学|小鼠肺组织Csf3rhiCD14hi中性粒细胞电离辐射前后转录组特征分析

小鼠肺组织Csf3rhiCD14hi中性粒细胞电离辐射前后转录组特征分析OA

Transcriptomic profiling of Csf3rhiCD14hi neutrophils in lung tissue of mice before and after irradiation

中文摘要英文摘要

目的 探讨由C3H/HeN小鼠肺组织分离的Csf3rhiCD14hi中性粒细胞(Neu)照射前后转录组特征.方法 将12只C3H/HeN小鼠随机分为对照组和照射组,单次胸部照射,剂量为20 Gy.照射后24周,采用流式细胞术由肺组织细胞分选对照组和照射组Csf3rhiCD14hiNeu和Csf3rlowCD14hiNeu 2种Neu亚群.通过RNA测序技术对2类细胞进行转录组测序(RNA-Seq),使用DESeq2软件筛选差异表达基因,并结合基因本体论(GO)和京都基因与基因组百科全书(KEGG)数据库进行功能富集分析及基因集富集分析(GSEA).结果 照射后24周,C3H/HeN小鼠肺泡腔面积显著减少,胶原沉积增加,出现局部纤维化.应用流式细胞术分选Csf3rhiCD14hiNeu与Csf3rlowCD14hiNeu,RNA-Seq结果表明,照射组Csf3rhiCD14hiNeu与Csf3rlowCD14hiNeu比较,存在1499个显著差异表达基因,其中179个上调,1320个下调;对照组Csf3rhiCD14hiNeu与Csf3rlowCD14hi Neu比较,显著上调基因701个,显著下调基因431个;照射组与对照组Csf3rlowCD14hi Neu比较,显著上调基因 1319 个,显著下调基因 219 个;照射组与对照组Csf3rhiCD14hiNeu比较,显著上调基因202个,显著下调基因540个.GO功能富集分析表明,这些差异表达基因参与免疫应答、Wnt信号通路及细胞因子生成.KEGG分析提示,其在TGF-β信号通路、细胞因子-细胞因子受体相互作用及Jak-STAT信号通路中显著富集.GSEA进一步显示,非经典NF-κB信号通路、PD-1信号转导及层粘连蛋白相互作用等相关通路存在显著差异.结论 γ射线胸部照射可导致 C3H/HeN 小鼠肺纤维化,其肺组织中Csf3rhiCD14hiNeu与Csf3rlowCD14hiNeu 2种Neu亚群在照射前后存在显著转录组差异.

Objective To investigate the transcription of neutrophils(Neu)expressing high levels of Csf3rhiCD14hiNeu in C3H/HeN mouse lung tissues before and after irradiation.Methods Twelve C3H/HeN mice were randomly divided into an irradiation group and a control group before being exposed to a single dose of 20 Gy chest irradiation.Twenty-four weeks after irradiation,two Neu subsets,Csf3rhiCD14hiNeu and Csf3rlowCD14hiNeu,were selected from lung tissues of irradiated and non-irradiated mice by flow cytometry.Transcriptomic sequencing(RNA-Seq)was performed on the two types of cells.Differentially expressed genes(DEGs)were identified using the DESeq2 package.Functional enrichment analysis and gene set enrichment analysis(GSEA)were performed using the gene ontology(GO)and Kyoto encyclopedia of genes and genomes(KEGG)databases.Results At 24 weeks post-irradiation,the alveolar space was significantly reduced,collagen deposition increased,and fibrosis localized in C3H/HeN mice.RNA-seq analysis suggested that there were 1499 DEGs in Csf3rhiCD14hi Neu compared with Csf3rlowCD14hi Neu in the irradiated group,179 of which were upregulated and 1320 downregulated.In the control group,there were 701 significantly upregulated and 431 downregulated genes in Csf3rhiCD14hi Neu compared with Csf3rlowCD14hi Neu.Compared with non-irradiated Csf3rlowCD14hi Neu,there were 1319 upregulated and 219 downregulated genes in the irradiated group.Compared with non-irradiated Csf3rhiCD14hi Neu,the irradiated group had 202 upregulated and 540 downregulated genes.GO enrichment analysis indicated that these DEGs were involved in immune response,Wnt signaling pathway,and cytokine production.KEGG pathway analysis pointed to significant enrichment in the TGF-β signaling pathway,cytokine-cytokine receptor interactions,and Jak-STAT signaling pathway.GSEA revealed significant alterations in non-canonical NF-κB signaling,PD-1 signaling,and laminin interaction-related pathways.Conclusion Thoracic γ-ray irradiation can cause pulmonary fibrosis in C3H/HeN mice,with marked transcriptomic differences between Csf3rhiCD14ʰⁱand Csf3rlowCD14hi Neu subsets in lung tissue post-irradiation.

邢玉洁;贾兆乾;冯婷;左红艳;李杨

军事科学院军事医学研究院,北京 100850军事科学院军事医学研究院,北京 100850河北大学,河北 保定 071000军事科学院军事医学研究院,北京 100850军事科学院军事医学研究院,北京 100850

医药卫生

电离辐射小鼠中性粒细胞放射性肺损伤RNA测序

radiationmiceneutrophilsradiation induced lung injuryRNA-sequencing

《军事医学》 2026 (4)

251-259,9

10.7644/j.issn.1674-9960.2026-00003

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