Liu Jinxia, Zhao Lingping, Li Chunsun, Jia Yali, Yang Zhen, Liang Zhixin, Wang Haiyang, Ma Xiuqing, Su Chengcheng, Ren Jiabo, Mo Zhenfei, Liu Wenli, Wu Peixin, Yin Yue, Liu Shangshu, Yue Wen, Xi Jiafei, Chen Liangan
Medical School of Chinese PLA, Beijing, China.
Beijing Institute of Radiation Medicine, Beijing, China.
J Thorac Dis. 2024 Nov 30;16(11):7836-7852. doi: 10.21037/jtd-24-1471. Epub 2024 Nov 25.
Seawater drowning (SWD) has been an escalating hazard in recent years. It can not only cause immediate death but can also inflict severe complications, such as acute lung injury (ALI), which greatly increases the mortality rate. Thus, investigating the mechanism of SWD induced lung injury and discovering effective treatments is of great importance. The aim of this study was to minimize the lethality and disability of SWD-ALI.
Using male C57BL/6 mice, we established a SWD induced ALI (SWD-ALI) model via the oral laryngoscopy endotracheal injection (LEI) of artificial seawater. We then administered mesenchymal stem cells (MSCs) via laryngoscopy endotracheal nebulized inhalation. We tested our hypotheses using pulmonary function tests, micro-computed tomography (Micro-CT), hematoxylin and eosin (HE) staining, Masson staining, immunofluorescence, immunoblotting, flow cytometry, transcriptome sequencing, quantitative real-time polymerase chain reaction (qPCR), and enzyme-linked immunosorbent assay (ELISA).
We successfully established the SWD-ALI model via LEI method of seawater. The results indicated that SWD induced severe ALI by activating the Snail-mediated epithelial-mesenchymal transition (EMT) pathway through the tumor necrosis factor alpha (TNFα) inflammatory response. Further, we administered transoral laryngoscopy endotracheal nebulization to the SWD mice treated with inhaled MSCs. Non-invasive pulmonary function tests revealed that the respiratory symptoms and respiratory function of the mice were significantly alleviated. Additionally, the histological injury and air-blood barrier, and inflammatory response were significantly mitigated, and TNFα-mediated Snail expression was significantly down-regulated. Importantly, we used Masson staining to examine mouse lung tissue after 28 days of drowning and found that the SWD mice suffered from significant long-term pulmonary fibrosis injury, and MSCs treatment significantly attenuated the degree of fibrosis.
Our research revealed that SWD triggered severe ALI, followed by long-term pulmonary fibrosis. However, treatment with nebulized MSCs significantly mitigated the ALI and slowed the progression of fibrosis.
近年来,海水溺水(SWD)的危害不断升级。它不仅可导致即刻死亡,还会引发严重并发症,如急性肺损伤(ALI),这大大增加了死亡率。因此,研究SWD诱导肺损伤的机制并发现有效的治疗方法至关重要。本研究的目的是将SWD-ALI的致死率和致残率降至最低。
我们使用雄性C57BL/6小鼠,通过经口喉镜气管内注射(LEI)人工海水建立SWD诱导的ALI(SWD-ALI)模型。然后通过喉镜气管内雾化吸入给予间充质干细胞(MSCs)。我们使用肺功能测试、微计算机断层扫描(Micro-CT)、苏木精和伊红(HE)染色、Masson染色、免疫荧光、免疫印迹、流式细胞术、转录组测序、定量实时聚合酶链反应(qPCR)和酶联免疫吸附测定(ELISA)来验证我们的假设。
我们通过LEI海水法成功建立了SWD-ALI模型。结果表明,SWD通过肿瘤坏死因子α(TNFα)炎症反应激活Snail介导的上皮-间质转化(EMT)途径,诱导严重的ALI。此外,我们对吸入MSCs治疗的SWD小鼠进行经口喉镜气管内雾化。无创肺功能测试显示,小鼠的呼吸道症状和呼吸功能得到显著缓解。此外,组织学损伤和气血屏障以及炎症反应显著减轻,TNFα介导的Snail表达显著下调。重要的是,我们在溺水28天后使用Masson染色检查小鼠肺组织,发现SWD小鼠存在明显的长期肺纤维化损伤,而MSCs治疗显著减轻了纤维化程度。
我们的研究表明,SWD引发严重的ALI,随后是长期的肺纤维化。然而,雾化MSCs治疗显著减轻了ALI并减缓了纤维化进程。