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Resveratrol pretreatment mitigates LPS-induced acute lung injury by regulating conventional dendritic cells’ maturation and function

Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) is a severe syndrome lacking efficient therapy and resulting in high morbidity and mortality. Although resveratrol (RES), a natural phytoalexin, has been reported to protect the ALI by suppressing the inflammatory response, the detai...

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Autores principales: Guo, Bingnan, Peng, Yigen, Gu, Yuting, Zhong, Yi, Su, Chenglei, Liu, Lin, Chai, Dafei, Song, Tengfei, Zhao, Ningjun, Yan, Xianliang, Xu, Tie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8483064/
https://www.ncbi.nlm.nih.gov/pubmed/34676301
http://dx.doi.org/10.1515/biol-2021-0110
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author Guo, Bingnan
Peng, Yigen
Gu, Yuting
Zhong, Yi
Su, Chenglei
Liu, Lin
Chai, Dafei
Song, Tengfei
Zhao, Ningjun
Yan, Xianliang
Xu, Tie
author_facet Guo, Bingnan
Peng, Yigen
Gu, Yuting
Zhong, Yi
Su, Chenglei
Liu, Lin
Chai, Dafei
Song, Tengfei
Zhao, Ningjun
Yan, Xianliang
Xu, Tie
author_sort Guo, Bingnan
collection PubMed
description Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) is a severe syndrome lacking efficient therapy and resulting in high morbidity and mortality. Although resveratrol (RES), a natural phytoalexin, has been reported to protect the ALI by suppressing the inflammatory response, the detailed mechanism of how RES affected the immune system is poorly studied. Pulmonary conventional dendritic cells (cDCs) are critically involved in the pathogenesis of inflammatory lung diseases including ALI. In this study, we aimed to investigate the protective role of RES via pulmonary cDCs in lipopolysaccharide (LPS)-induced ALI mice. Murine ALI model was established by intratracheally challenging with 5 mg/kg LPS. We found that RES pretreatment could mitigate LPS-induced ALI. Additionally, proinflammatory-skewed cytokines decreased whereas anti-inflammatory-related cytokines increased in bronchoalveolar lavage fluid by RES pretreatment. Mechanistically, RES regulated pulmonary cDCs’ maturation and function, exhibiting lower level of CD80, CD86, major histocompatibility complex (MHC) II expression, and IL-10 secretion in ALI mice. Furthermore, RES modulated the balance between proinflammation and anti-inflammation of cDCs. Moreover, in vitro RES pretreatment regulated the maturation and function of bone marrow derived dendritic cells (BMDCs). Finally, the adoptive transfer of RES-pretreated BMDCs enhanced recovery of ALI. Thus, these data might further extend our understanding of a protective role of RES in regulating pulmonary cDCs against ALI.
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spelling pubmed-84830642021-10-20 Resveratrol pretreatment mitigates LPS-induced acute lung injury by regulating conventional dendritic cells’ maturation and function Guo, Bingnan Peng, Yigen Gu, Yuting Zhong, Yi Su, Chenglei Liu, Lin Chai, Dafei Song, Tengfei Zhao, Ningjun Yan, Xianliang Xu, Tie Open Life Sci Research Article Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) is a severe syndrome lacking efficient therapy and resulting in high morbidity and mortality. Although resveratrol (RES), a natural phytoalexin, has been reported to protect the ALI by suppressing the inflammatory response, the detailed mechanism of how RES affected the immune system is poorly studied. Pulmonary conventional dendritic cells (cDCs) are critically involved in the pathogenesis of inflammatory lung diseases including ALI. In this study, we aimed to investigate the protective role of RES via pulmonary cDCs in lipopolysaccharide (LPS)-induced ALI mice. Murine ALI model was established by intratracheally challenging with 5 mg/kg LPS. We found that RES pretreatment could mitigate LPS-induced ALI. Additionally, proinflammatory-skewed cytokines decreased whereas anti-inflammatory-related cytokines increased in bronchoalveolar lavage fluid by RES pretreatment. Mechanistically, RES regulated pulmonary cDCs’ maturation and function, exhibiting lower level of CD80, CD86, major histocompatibility complex (MHC) II expression, and IL-10 secretion in ALI mice. Furthermore, RES modulated the balance between proinflammation and anti-inflammation of cDCs. Moreover, in vitro RES pretreatment regulated the maturation and function of bone marrow derived dendritic cells (BMDCs). Finally, the adoptive transfer of RES-pretreated BMDCs enhanced recovery of ALI. Thus, these data might further extend our understanding of a protective role of RES in regulating pulmonary cDCs against ALI. De Gruyter 2021-09-29 /pmc/articles/PMC8483064/ /pubmed/34676301 http://dx.doi.org/10.1515/biol-2021-0110 Text en © 2021 Bingnan Guo et al., published by De Gruyter https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License.
spellingShingle Research Article
Guo, Bingnan
Peng, Yigen
Gu, Yuting
Zhong, Yi
Su, Chenglei
Liu, Lin
Chai, Dafei
Song, Tengfei
Zhao, Ningjun
Yan, Xianliang
Xu, Tie
Resveratrol pretreatment mitigates LPS-induced acute lung injury by regulating conventional dendritic cells’ maturation and function
title Resveratrol pretreatment mitigates LPS-induced acute lung injury by regulating conventional dendritic cells’ maturation and function
title_full Resveratrol pretreatment mitigates LPS-induced acute lung injury by regulating conventional dendritic cells’ maturation and function
title_fullStr Resveratrol pretreatment mitigates LPS-induced acute lung injury by regulating conventional dendritic cells’ maturation and function
title_full_unstemmed Resveratrol pretreatment mitigates LPS-induced acute lung injury by regulating conventional dendritic cells’ maturation and function
title_short Resveratrol pretreatment mitigates LPS-induced acute lung injury by regulating conventional dendritic cells’ maturation and function
title_sort resveratrol pretreatment mitigates lps-induced acute lung injury by regulating conventional dendritic cells’ maturation and function
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8483064/
https://www.ncbi.nlm.nih.gov/pubmed/34676301
http://dx.doi.org/10.1515/biol-2021-0110
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