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Neutrophil extracellular traps contribute to the pathogenesis of acid-aspiration-induced ALI/ARDS
BACKGROUND: 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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788598/ https://www.ncbi.nlm.nih.gov/pubmed/29416730 http://dx.doi.org/10.18632/oncotarget.22744 |
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author | 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 |
author_facet | 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 |
author_sort | Li, Haitao |
collection | PubMed |
description | BACKGROUND: 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. RESULTS: Analysis of bronchial aspirates from ARDS patients showed that NETs were significantly correlated with the degree of ARDS (r = –0.5846, p = 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; p = 0.003, n = 5 per group). Exogenous NETs aggravated lung injury, while alvelestat and DNase markedly attenuated the intensity of ARDS. MATERIALS AND METHODS: 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. CONCLUSIONS: NETs may contribute to ALI/ARDS by promoting tissue damage and systemic inflammation. Targeting NETs by alvelestat may be a potential therapeutic strategy. |
format | Online Article Text |
id | pubmed-5788598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57885982018-02-07 Neutrophil extracellular traps contribute to the pathogenesis of acid-aspiration-induced ALI/ARDS 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 Oncotarget Research Paper BACKGROUND: 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. RESULTS: Analysis of bronchial aspirates from ARDS patients showed that NETs were significantly correlated with the degree of ARDS (r = –0.5846, p = 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; p = 0.003, n = 5 per group). Exogenous NETs aggravated lung injury, while alvelestat and DNase markedly attenuated the intensity of ARDS. MATERIALS AND METHODS: 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. CONCLUSIONS: NETs may contribute to ALI/ARDS by promoting tissue damage and systemic inflammation. Targeting NETs by alvelestat may be a potential therapeutic strategy. Impact Journals LLC 2017-11-28 /pmc/articles/PMC5788598/ /pubmed/29416730 http://dx.doi.org/10.18632/oncotarget.22744 Text en Copyright: © 2018 Li et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper 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 Neutrophil extracellular traps contribute to the pathogenesis of acid-aspiration-induced ALI/ARDS |
title | Neutrophil extracellular traps contribute to the pathogenesis of acid-aspiration-induced ALI/ARDS |
title_full | Neutrophil extracellular traps contribute to the pathogenesis of acid-aspiration-induced ALI/ARDS |
title_fullStr | Neutrophil extracellular traps contribute to the pathogenesis of acid-aspiration-induced ALI/ARDS |
title_full_unstemmed | Neutrophil extracellular traps contribute to the pathogenesis of acid-aspiration-induced ALI/ARDS |
title_short | Neutrophil extracellular traps contribute to the pathogenesis of acid-aspiration-induced ALI/ARDS |
title_sort | neutrophil extracellular traps contribute to the pathogenesis of acid-aspiration-induced ali/ards |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788598/ https://www.ncbi.nlm.nih.gov/pubmed/29416730 http://dx.doi.org/10.18632/oncotarget.22744 |
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