Li Haitao, Zhou Xiaoting, Tan Hongyi, Hu Yongbin, Zhang Lemeng, Liu Shuai, Dai Minhui, Li Yi, Li Qian, Mao Zhi, Pan Pinhua, Su Xiaoli, Hu Chengpin
Department of Pulmonary and Critical Care Medicine, Key Site of National Clinical Research Centre for Respiratory Disease, Xiangya Hospital, Central South University, Changsha 410008, China.
Department of Neurology, Xiangya Hospital, Central South University, Changsha 410008, China.
Oncotarget. 2017 Nov 28;9(2):1772-1784. doi: 10.18632/oncotarget.22744. eCollection 2018 Jan 5.
Acute lung injury/acute respiratory distress syndrome (ALI/ARDS) is a manifestation of systemic inflammation in the lungs, but the factors that trigger inflammation in ALI/ARDS are unclear. We hypothesized that neutrophil extracellular traps (NETs) contribute to the pathogenesis of acid aspiration-induced ALI/ARDS.
Analysis of bronchial aspirates from ARDS patients showed that NETs were significantly correlated with the degree of ARDS (r = -0.5846, = 0.0359). NETs in bronchoalveolar lavage fluid of acid-aspiration mice were significantly higher (141.6 ± 23.08) at 3 h after injury than those in the sham group (1234 ± 101.9; = 0.003, = 5 per group). Exogenous NETs aggravated lung injury, while alvelestat and DNase markedly attenuated the intensity of ARDS.
We investigated whether NETs are involved in the severity of gastric aspiration-induced ARDS. Then, a hydrochloric acid aspiration-induced ALI murine model was used to assess whether NETs are pathogenic and whether targeting NETs is protective. Exogenous NETs were administered to mice. Alvelestat can inhibit neutrophil elastase (NE), which serves an important role in NET formation, so we investigated whether alvelestat could protect against ALI in cell and mouse models.
NETs may contribute to ALI/ARDS by promoting tissue damage and systemic inflammation. Targeting NETs by alvelestat may be a potential therapeutic strategy.
急性肺损伤/急性呼吸窘迫综合征(ALI/ARDS)是肺部系统性炎症的一种表现,但引发ALI/ARDS炎症的因素尚不清楚。我们推测中性粒细胞胞外陷阱(NETs)参与了酸吸入诱导的ALI/ARDS的发病机制。
对ARDS患者支气管吸出物的分析表明,NETs与ARDS程度显著相关(r = -0.5846,P = 0.0359)。酸吸入小鼠支气管肺泡灌洗液中的NETs在损伤后3小时显著高于假手术组(141.6 ± 23.08 vs 1234 ± 101.9;P = 0.003,每组n = 5)。外源性NETs加重了肺损伤,而阿弗司他和脱氧核糖核酸酶显著减轻了ARDS的严重程度。
我们研究了NETs是否参与胃内容物吸入诱导的ARDS的严重程度。然后,使用盐酸吸入诱导的ALI小鼠模型来评估NETs是否具有致病性以及靶向NETs是否具有保护作用。将外源性NETs给予小鼠。阿弗司他可抑制在NET形成中起重要作用的中性粒细胞弹性蛋白酶(NE),因此我们研究了阿弗司他在细胞和小鼠模型中是否能预防ALI。
NETs可能通过促进组织损伤和全身炎症而导致ALI/ARDS。用阿弗司他靶向NETs可能是一种潜在的治疗策略。