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基于蛋白组学探讨放射性肺损伤致病机制

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目的 基于蛋白组学探讨放射性肺损伤的作用机制.方法 将20 只体质量180~220 g的健康雄性SD大鼠随机分入对照组和放射组(大鼠肺部20 Gy照射),每组各10 只.运用直线加速器单次照射20 Gy构建放射性肺损伤动物模型.处死大鼠后取全肺组织标本,提取蛋白,基于液相色谱-串联质谱技术进行蛋白组学检测,通过DAVID进行生信分析,分析放射性肺损伤后的差异蛋白,根据放射性肺损伤整体炎症蛋白的变化特征筛选出有意义的通路.结果 通过蛋白质定量筛选,在对照组和放射组中筛选出差异蛋白200 个;根据炎症相关蛋白富集分析筛选出最有意义的 9 个通路,包括炎症反应的调节、转化生长因子-β受体信号通路的正调控、黏膜固有免疫反应、白细胞介素-7 的细胞反应、白细胞介素-8 产生的正调节、NIK/NF-kappaB信号的正调控、中性粒细胞趋化性的正调控、中性粒细胞趋化性、通过T细胞受体与抗原呈递细胞上MHC分子结合的抗原接触激活T细胞.结论 放射性肺损伤可能与炎症反应、抗氧化应激及炎症调控蛋白表达密切相关.
Pathogenic mechanism of radiation-induced acute lung injury based on proteomics
Objective To investigate the pathogenic mechanism of radiation-induced acute lung injury in rats based on proteomics.Methods Twenty healthy male SD rats with body weight of 180-220 grams were randomly divided into control group and radiation group(20 Gy lung irradiation of rats),with 10 rats in each group.The animal model of lung injury was established by linear accelerator irradiation of 20 Gy.After the rats were killed,whole lung tissue samples were taken,proteins were extracted,and proteomic detection was carried out based on liquid chromatography tandem mass spectrometry.The differential proteins after radiation lung injury were an-alyzed through biogenic analysis by DAVID,and meaningful pathways were screened according to the change characteristics of the o-verall inflammatory proteins after radiation lung injury.Results Through protein quantitative screening,200 differentially expressed proteins were screened out between the radiation group and the control group.According to the results of enrichment analysis of inflam-mation-related proteins,the most significant 9 pathways were screened out,including the regulation of the inflammatory response,posi-tive regulation of transforming growth factor-β receptor signaling pathway,mucosal cells of the innate immune response,interleukin-7 reaction,positive regulation of interleukin-8 production,positive regulation of NIK/NF-kappaB signals,positive regulation of neutrophil chemotaxis,neutrophil chemotaxis,activation of T cells by antigenic contact with T cell receptors bound to MHC molecules on antigen-presenting cells.Conclusion Radiation lung injury may be closely related to inflammatory response,antioxidant stress and expression of inflammatory regulatory proteins.

Radiation lung injuryProteomicsInflammatory responseLiquid chromatography tandem mass spectrometry

武忠宝、徐莹、柳云恩、阎英

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北部战区总医院 放疗科,辽宁 沈阳 110016

沈阳医学院,辽宁 沈阳 110000

放射性肺损伤 蛋白组学 炎症反应 液相色谱-串联质谱技术

辽宁省科学技术计划项目军队后勤科研重点课题

2020JH2/10300172BLB19J012

2024

临床军医杂志
解放军沈阳军区卫生人员训练基地

临床军医杂志

CSTPCD
影响因子:0.465
ISSN:1671-3826
年,卷(期):2024.52(7)
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