基于NLRP3/Caspase-1/GSDMD焦亡通路探索小鼠急性肺损伤动态时间模型的建立
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中国中医科学院西苑医院

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国家自然科学基金项目(面上项目,重点项目,重大项目)


Exploration of establishing the dynamic time model of acute lung injury in mice based on the NLRP3/caspase-1/GSDMD signal pyroptosis pathway
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Xiyuan Hospital, China Academy of Chinese Medical Sciences

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    目的:基于NLRP3/Caspase-1/GSDMD焦亡通路,建立随时间变化的脂多糖诱导的急性肺损伤小鼠模型,观察不同时间点小鼠肺损伤情况,根据不同时间伤情的变化和焦亡通路相关蛋白的表达,综合筛选出最佳造模时间点,为后续实验奠定动物模型基础。方法:54只6-8周龄SPF级雄性BAL b/c小鼠,随机分为9组,空白对照组和造模时间组(1、3、6、12、18、24、48和72 h组),分别检测体重、肺组织大体、病理观察及半定量评分、肺指数、肺含水量及湿干重比;取肺泡灌洗液检测白细胞计数,TNF-α、IL-6、IL-1β、IL-18及BCA蛋白浓度;使用免疫印迹法检测肺组织中经典焦亡通路相关NLRP3、pro-Caspase-1、Caspase-1、GSDMD蛋白的表达。结果:根据体重统计,各组体重均有下降,24h及48h组体重下降最为明显;通过肺组织大体、病理观察及评分发现,24h-72h肺组织损伤严重,每组与Con组比较均有统计学意义;肺指数、肺含水量及湿干重比在24-72h明显升高;肺泡灌洗液中白细胞从造模后6h开始升高,48h可达峰值,至72h均维持上升状态;灌洗液中IL-18在24h开始升高,72h仍然保持持续升高趋势;TNF-α、IL-1β、IL-6炎症因子在6h时均保持最高水平状态,在48h明显降低;灌洗液中蛋白浓度在24h、48h及72h与Con组相比均有明显升高;通过免疫印迹法检测发现,ALI模型各个时间组焦亡通路蛋白NLRP3、pro-Caspase-1、Caspase-1与GSDMD蛋白表达均有上调,24 h-72h组的通路蛋白表达与对照组相比明显增强。结论:综合分析不同时间组中各项实验指标、炎症因子及WB中通路蛋白的表达,发现焦亡机制与ALI的发生与进展密切相关,并随时间迁移,从实验结果得知24h-48h肺损伤程度严重,肺损伤相关指标及通路蛋白具有研究意义,可作为造模时间参考,也为后续研究ALI的具体机制及干预靶点提供了模型参考与实验基础。

    Abstract:

    Objective: Based on the NLRP3/Caspase-1/GSDMD pyroptosis pathway, a mouse model of LPS-induced acute lung injury was established over time, and the lung injury of mice was observed at different time points. According to the changes in injury at different time points and the expression of pyroptosis pathway-related proteins, the best time point for modeling was screened comprehensively, which laid the foundation for animal models for subsequent experiments. Methods: 54 six to eight weeks of SPF male BAL b/c mice were divided into nine groups randomly, which including control group and building time group (1, 3, 6, 12, 18, 24, 48 and 72 h group), body weight, lung tissue was detected in general and pathological observation and semi-quantitative score, lung index, lung water content of wet and dry weight ratio; The white blood cell count and the concentrations of tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), interleukin-1β (IL-1β), IL-18 and BCA protein in bronchoalveolar lavage fluid (BALF) were detected. Using western blot method to detect the lung tissue of classic coke death pathways related NLRP3, pro - Caspase 1, Caspase 1, GSDMD protein expression. Results: According to the body weight statistics, the body weight of each group decreased, and the 24h and 48h groups showed the most significant weight loss. The results of gross observation and pathological examination of lung tissue showed that the injury of lung tissue in 24h to 72h was severe, and the difference between each group and Con group was statistically significant. Lung index, lung water content and wet/dry weight ratio were significantly increased at 24-72 hours. Alveolar lavage fluid white blood cells from 6 h after building began to rise, 48 h can reach a peak, 72 h all keep increasing; IL-18 in lavage fluid began to increase at 24 hours and continued to increase at 72 hours. TNF alpha, beta, IL - 6, IL - 1 inflammatory factors were keep the highest level at the time of 6 h, 48 h significantly reduced; A lavage in protein concentrations within 24 h, 48 h and 72 h compared with Con group were significantly increased; Found by western blot method and ALI model each time series jiao wu pathway proteins NLRP3, pro - Caspase 1, Caspase 1 and GSDMD protein expression were raised, 24 h - 72 - h group of channel protein expression enhanced significantly compared with control subjects. Conclusions: Comprehensive analysis of the experimental indicators, inflammatory factors and the expression of pathway proteins in WB in different time groups showed that the mechanism of pyroptosis was closely related to the occurrence and progression of ALI, and it moved with time. From the experimental results, it was found that the expression of pyroptosis pathway was the most obvious and the lung injury was the most serious in 24h-48h. This study provides a model reference and experimental basis for the subsequent study of the specific mechanism and intervention targets of ALI.

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  • 收稿日期:2023-12-06
  • 最后修改日期:2024-04-03
  • 录用日期:2024-04-07
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