Mangiferin Mitigates Lipopolysaccharide-Induced Lung Injury by Inhibiting NLRP3 Inflammasome Activation

Ning Li,* Rui Xiong,* Ruyuan He, Bohao Liu, Bo Wang, Qing Geng Department of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, 430060, People’s Republic of China*These authors contributed equally to this workCorrespondence: Bo Wang; Qing GengDepartment of Thoracic Surgery, Renm...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Li N, Xiong R, He R, Liu B, Wang B, Geng Q
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2021
Materias:
p65
Acceso en línea:https://doaj.org/article/65ccaf0097c24bb9a766b278a063020f
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:65ccaf0097c24bb9a766b278a063020f
record_format dspace
spelling oai:doaj.org-article:65ccaf0097c24bb9a766b278a063020f2021-12-02T16:58:44ZMangiferin Mitigates Lipopolysaccharide-Induced Lung Injury by Inhibiting NLRP3 Inflammasome Activation1178-7031https://doaj.org/article/65ccaf0097c24bb9a766b278a063020f2021-05-01T00:00:00Zhttps://www.dovepress.com/mangiferin-mitigates-lipopolysaccharide-induced-lung-injury-by-inhibit-peer-reviewed-fulltext-article-JIRhttps://doaj.org/toc/1178-7031Ning Li,* Rui Xiong,* Ruyuan He, Bohao Liu, Bo Wang, Qing Geng Department of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, 430060, People’s Republic of China*These authors contributed equally to this workCorrespondence: Bo Wang; Qing GengDepartment of Thoracic Surgery, Renmin Hospital of Wuhan University, Jiefang Road 238, Wuhan, 430060, People’s Republic of ChinaEmail rmh_wb@whu.edu.cn; gengqingwhu@whu.edu.cnScope: Mangiferin (MF) is a natural phytopolyphenol, which displays potential pharmacological properties involving antibacterial, anti-inflammation, antioxidant and anti-tumor. However, little is known about the roles of MF in lung injury. The aim of this study is to demonstrate the modulatory effects and molecular mechanisms by which MF operates in sepsis-induced lung injury.Methods and Results: To examine the protective properties of MF, an in vivo model of lipopolysaccharide (LPS)-induced lung injury in mice and an in vitro model of LPS-treated J774A.1 cells were established, respectively. The results revealed that MF treatment significantly relieved LPS-induced pathological injury and inflammatory response in murine lung tissues. Meanwhile, MF treatment also inhibited nucleotide-binding oligomerization domain (NOD)-like receptor family, pyrin domain-containing protein 3 (NLRP3) inflammasome activation and pyroptosis induced by LPS. In macrophage-specific NLRP3 deficiency mice treated with LPS, MF showed little protective effects. NLRP3 overexpression by adenovirus could also offset the beneficial effects of MF in LPS-treated J774A.1 cells. Furthermore, we found that MF could suppress the expression of NLPR3 and pyroptosis of macrophages by inhibiting the nuclear translocation of the nuclear factor-κB (NF-κB) subunits P50 and P65.Conclusion: MF protects against lung injury and inflammatory response by inhibiting NLRP3 inflammasome activation in a NF-κB-dependent manner in macrophages, which provides a promising therapeutic candidate for the treatment of lung injury.Keywords: mangiferin, lung injury, NLRP3, P65Li NXiong RHe RLiu BWang BGeng QDove Medical Pressarticlemangiferinlung injurynlrp3p65PathologyRB1-214Therapeutics. PharmacologyRM1-950ENJournal of Inflammation Research, Vol Volume 14, Pp 2289-2300 (2021)
institution DOAJ
collection DOAJ
language EN
topic mangiferin
lung injury
nlrp3
p65
Pathology
RB1-214
Therapeutics. Pharmacology
RM1-950
spellingShingle mangiferin
lung injury
nlrp3
p65
Pathology
RB1-214
Therapeutics. Pharmacology
RM1-950
Li N
Xiong R
He R
Liu B
Wang B
Geng Q
Mangiferin Mitigates Lipopolysaccharide-Induced Lung Injury by Inhibiting NLRP3 Inflammasome Activation
description Ning Li,* Rui Xiong,* Ruyuan He, Bohao Liu, Bo Wang, Qing Geng Department of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, 430060, People’s Republic of China*These authors contributed equally to this workCorrespondence: Bo Wang; Qing GengDepartment of Thoracic Surgery, Renmin Hospital of Wuhan University, Jiefang Road 238, Wuhan, 430060, People’s Republic of ChinaEmail rmh_wb@whu.edu.cn; gengqingwhu@whu.edu.cnScope: Mangiferin (MF) is a natural phytopolyphenol, which displays potential pharmacological properties involving antibacterial, anti-inflammation, antioxidant and anti-tumor. However, little is known about the roles of MF in lung injury. The aim of this study is to demonstrate the modulatory effects and molecular mechanisms by which MF operates in sepsis-induced lung injury.Methods and Results: To examine the protective properties of MF, an in vivo model of lipopolysaccharide (LPS)-induced lung injury in mice and an in vitro model of LPS-treated J774A.1 cells were established, respectively. The results revealed that MF treatment significantly relieved LPS-induced pathological injury and inflammatory response in murine lung tissues. Meanwhile, MF treatment also inhibited nucleotide-binding oligomerization domain (NOD)-like receptor family, pyrin domain-containing protein 3 (NLRP3) inflammasome activation and pyroptosis induced by LPS. In macrophage-specific NLRP3 deficiency mice treated with LPS, MF showed little protective effects. NLRP3 overexpression by adenovirus could also offset the beneficial effects of MF in LPS-treated J774A.1 cells. Furthermore, we found that MF could suppress the expression of NLPR3 and pyroptosis of macrophages by inhibiting the nuclear translocation of the nuclear factor-κB (NF-κB) subunits P50 and P65.Conclusion: MF protects against lung injury and inflammatory response by inhibiting NLRP3 inflammasome activation in a NF-κB-dependent manner in macrophages, which provides a promising therapeutic candidate for the treatment of lung injury.Keywords: mangiferin, lung injury, NLRP3, P65
format article
author Li N
Xiong R
He R
Liu B
Wang B
Geng Q
author_facet Li N
Xiong R
He R
Liu B
Wang B
Geng Q
author_sort Li N
title Mangiferin Mitigates Lipopolysaccharide-Induced Lung Injury by Inhibiting NLRP3 Inflammasome Activation
title_short Mangiferin Mitigates Lipopolysaccharide-Induced Lung Injury by Inhibiting NLRP3 Inflammasome Activation
title_full Mangiferin Mitigates Lipopolysaccharide-Induced Lung Injury by Inhibiting NLRP3 Inflammasome Activation
title_fullStr Mangiferin Mitigates Lipopolysaccharide-Induced Lung Injury by Inhibiting NLRP3 Inflammasome Activation
title_full_unstemmed Mangiferin Mitigates Lipopolysaccharide-Induced Lung Injury by Inhibiting NLRP3 Inflammasome Activation
title_sort mangiferin mitigates lipopolysaccharide-induced lung injury by inhibiting nlrp3 inflammasome activation
publisher Dove Medical Press
publishDate 2021
url https://doaj.org/article/65ccaf0097c24bb9a766b278a063020f
work_keys_str_mv AT lin mangiferinmitigateslipopolysaccharideinducedlunginjurybyinhibitingnlrp3inflammasomeactivation
AT xiongr mangiferinmitigateslipopolysaccharideinducedlunginjurybyinhibitingnlrp3inflammasomeactivation
AT her mangiferinmitigateslipopolysaccharideinducedlunginjurybyinhibitingnlrp3inflammasomeactivation
AT liub mangiferinmitigateslipopolysaccharideinducedlunginjurybyinhibitingnlrp3inflammasomeactivation
AT wangb mangiferinmitigateslipopolysaccharideinducedlunginjurybyinhibitingnlrp3inflammasomeactivation
AT gengq mangiferinmitigateslipopolysaccharideinducedlunginjurybyinhibitingnlrp3inflammasomeactivation
_version_ 1718382269359456256