Guo Bingnan, Peng Yigen, Gu Yuting, Zhong Yi, Su Chenglei, Liu Lin, Chai Dafei, Song Tengfei, Zhao Ningjun, Yan Xianliang, Xu Tie
Jiangsu Institute of Health Emergency, Xuzhou Medical University, Xuzhou, Jiangsu 221004, China.
Department of Emergency Medicine, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu 221000, China.
Open Life Sci. 2021 Sep 29;16(1):1064-1081. doi: 10.1515/biol-2021-0110. eCollection 2021.
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, 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.
急性肺损伤(ALI)/急性呼吸窘迫综合征(ARDS)是一种缺乏有效治疗方法且导致高发病率和死亡率的严重综合征。尽管白藜芦醇(RES),一种天然植保素,已被报道可通过抑制炎症反应来保护ALI,但RES影响免疫系统的详细机制研究较少。肺常规树突状细胞(cDCs)在包括ALI在内的炎症性肺病的发病机制中起关键作用。在本研究中,我们旨在研究RES通过肺cDCs在脂多糖(LPS)诱导的ALI小鼠中的保护作用。通过气管内给予5 mg/kg LPS建立小鼠ALI模型。我们发现RES预处理可减轻LPS诱导的ALI。此外,RES预处理使支气管肺泡灌洗液中促炎倾向的细胞因子减少,而抗炎相关细胞因子增加。机制上,RES调节肺cDCs的成熟和功能,在ALI小鼠中表现出较低水平的CD80、CD86、主要组织相容性复合体(MHC)II表达和IL-10分泌。此外,RES调节cDCs促炎和抗炎之间的平衡。而且,RES预处理调节骨髓来源树突状细胞(BMDCs)的成熟和功能。最后,RES预处理的BMDCs的过继转移增强了ALI的恢复。因此,这些数据可能进一步扩展我们对RES在调节肺cDCs抵抗ALI中的保护作用的理解。