Protective effect of TM6 on LPS-induced acute lung injury in mice

Abstract Acute lung injury (ALI) is an acute failure of the respiratory system for which effective treatment is urgently necessary. Previous studies found that several peptides potently inhibited the production of cytokines induced by lipopolysaccharide (LPS). In this study, we synthetized a cell-pe...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Xiaoyu Hu, Yuan Tian, Shihui Qu, Yongguo Cao, Shumin Li, Wenlong Zhang, Zecai Zhang, Naisheng Zhang, Yunhe Fu
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2017
Materias:
R
Q
Acceso en línea:https://doaj.org/article/65fbb1a0f78b465588c2b87c22d571ed
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:65fbb1a0f78b465588c2b87c22d571ed
record_format dspace
spelling oai:doaj.org-article:65fbb1a0f78b465588c2b87c22d571ed2021-12-02T11:52:30ZProtective effect of TM6 on LPS-induced acute lung injury in mice10.1038/s41598-017-00551-82045-2322https://doaj.org/article/65fbb1a0f78b465588c2b87c22d571ed2017-04-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-00551-8https://doaj.org/toc/2045-2322Abstract Acute lung injury (ALI) is an acute failure of the respiratory system for which effective treatment is urgently necessary. Previous studies found that several peptides potently inhibited the production of cytokines induced by lipopolysaccharide (LPS). In this study, we synthetized a cell-permeable TIR domain-derived decoy peptide (TM6) and examined its substance for the ability to inhibit TLR signaling in the model of ALI induced by LPS. We demonstrated that TM6 (2.5, 5 and 10 nmol/g) alleviated the histological changes in the lung tissues as well as myeloperoxtidase (MPO) activity, lung W/D ratio, the production of TNF-α, IL-1β and IL-6 induced by LPS. Furthermore, the numbers of total cells, neutrophils and macrophages in the BALF were suppressed by TM6. In vitro, TM6 (5, 10 and 20 µM) inhibited the production of TNF-α, IL-1β and IL-6 in LPS-stimulated alveolar macrophages. Moreover, the activation of Nuclear factor-kappaB (NF-κB) and Mitogen activated protein kinases (MAPK) signaling pathways induced by LPS were also inhibited by TM6. Collectively, our results suggested that TM6 was an effective inhibitor of ALI induced by LPS, and this peptide may very well serve as a future treatment for ALI.Xiaoyu HuYuan TianShihui QuYongguo CaoShumin LiWenlong ZhangZecai ZhangNaisheng ZhangYunhe FuNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Xiaoyu Hu
Yuan Tian
Shihui Qu
Yongguo Cao
Shumin Li
Wenlong Zhang
Zecai Zhang
Naisheng Zhang
Yunhe Fu
Protective effect of TM6 on LPS-induced acute lung injury in mice
description Abstract Acute lung injury (ALI) is an acute failure of the respiratory system for which effective treatment is urgently necessary. Previous studies found that several peptides potently inhibited the production of cytokines induced by lipopolysaccharide (LPS). In this study, we synthetized a cell-permeable TIR domain-derived decoy peptide (TM6) and examined its substance for the ability to inhibit TLR signaling in the model of ALI induced by LPS. We demonstrated that TM6 (2.5, 5 and 10 nmol/g) alleviated the histological changes in the lung tissues as well as myeloperoxtidase (MPO) activity, lung W/D ratio, the production of TNF-α, IL-1β and IL-6 induced by LPS. Furthermore, the numbers of total cells, neutrophils and macrophages in the BALF were suppressed by TM6. In vitro, TM6 (5, 10 and 20 µM) inhibited the production of TNF-α, IL-1β and IL-6 in LPS-stimulated alveolar macrophages. Moreover, the activation of Nuclear factor-kappaB (NF-κB) and Mitogen activated protein kinases (MAPK) signaling pathways induced by LPS were also inhibited by TM6. Collectively, our results suggested that TM6 was an effective inhibitor of ALI induced by LPS, and this peptide may very well serve as a future treatment for ALI.
format article
author Xiaoyu Hu
Yuan Tian
Shihui Qu
Yongguo Cao
Shumin Li
Wenlong Zhang
Zecai Zhang
Naisheng Zhang
Yunhe Fu
author_facet Xiaoyu Hu
Yuan Tian
Shihui Qu
Yongguo Cao
Shumin Li
Wenlong Zhang
Zecai Zhang
Naisheng Zhang
Yunhe Fu
author_sort Xiaoyu Hu
title Protective effect of TM6 on LPS-induced acute lung injury in mice
title_short Protective effect of TM6 on LPS-induced acute lung injury in mice
title_full Protective effect of TM6 on LPS-induced acute lung injury in mice
title_fullStr Protective effect of TM6 on LPS-induced acute lung injury in mice
title_full_unstemmed Protective effect of TM6 on LPS-induced acute lung injury in mice
title_sort protective effect of tm6 on lps-induced acute lung injury in mice
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/65fbb1a0f78b465588c2b87c22d571ed
work_keys_str_mv AT xiaoyuhu protectiveeffectoftm6onlpsinducedacutelunginjuryinmice
AT yuantian protectiveeffectoftm6onlpsinducedacutelunginjuryinmice
AT shihuiqu protectiveeffectoftm6onlpsinducedacutelunginjuryinmice
AT yongguocao protectiveeffectoftm6onlpsinducedacutelunginjuryinmice
AT shuminli protectiveeffectoftm6onlpsinducedacutelunginjuryinmice
AT wenlongzhang protectiveeffectoftm6onlpsinducedacutelunginjuryinmice
AT zecaizhang protectiveeffectoftm6onlpsinducedacutelunginjuryinmice
AT naishengzhang protectiveeffectoftm6onlpsinducedacutelunginjuryinmice
AT yunhefu protectiveeffectoftm6onlpsinducedacutelunginjuryinmice
_version_ 1718395050044424192