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多不饱和脂肪酸通过差异调节病原体识别和 p38 MAPK/NF-κB 信号通路影响 LPS 诱导的鱼类巨噬细胞炎症反应。

Polyunsaturated Fatty Acids Influence LPS-Induced Inflammation of Fish Macrophages Through Differential Modulation of Pathogen Recognition and p38 MAPK/NF-κB Signaling.

机构信息

Key Laboratory of Aquaculture Nutrition and Feed (Ministry of Agriculture) & Key Laboratory of Mariculture (Ministry of Education), College of Fisheries, Ocean University of China, Qingdao, China.

Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China.

出版信息

Front Immunol. 2020 Oct 6;11:559332. doi: 10.3389/fimmu.2020.559332. eCollection 2020.

Abstract

Polyunsaturated fatty acids (PUFAs) not only serve as essential nutrients but also function as modulators of the immune response in marine fish. However, their immunomodulatory mechanism is poorly understood given that the underlying regulation of the innate immune response in fish has not been fully elucidated. Hence, study of the innate immunity of fish could help elucidate the mechanism by which PUFAs affect the fish immune response. Here, we used combined transcriptome analysis and experimentation to study the mechanism of LPS-induced inflammation. Transcriptome profiling indicated that LPS elicited strong pro-inflammatory responses featuring high expression levels of pathogen recognition receptors (PRRs) and cytokines along with the activation of NF-κB and MAPK signaling pathways. The transcription factor p65 alone could increase the transcription of by binding to the promoter of , and this promoting effect disappeared after mutation or deletion of its binding sites. We then examined the effects of PUFAs on the levels of gene expression and the abundance of proteins of critical kinases associated with LPS-induced inflammation. We found that LA exerts pro-inflammatory response while ALA, EPA, and DHA induced anti-inflammatory effects by modulating the expression of PRRs, phosphorylation of IKK and p38, and the nuclear translocation of p65. Overall, this study advances our understanding of the regulatory mechanisms by which PUFAs regulate LPS-induced inflammation in a non-model fish species.

摘要

多不饱和脂肪酸(PUFAs)不仅是必需的营养物质,还作为海洋鱼类免疫反应的调节剂。然而,由于鱼类先天免疫反应的潜在调控机制尚未完全阐明,因此它们的免疫调节机制还不太清楚。因此,研究鱼类的先天免疫可以帮助阐明 PUFAs 影响鱼类免疫反应的机制。在这里,我们使用组合转录组分析和实验来研究 LPS 诱导炎症的机制。转录组谱分析表明,LPS 引发了强烈的促炎反应,特征是病原体识别受体(PRRs)和细胞因子的高水平表达,以及 NF-κB 和 MAPK 信号通路的激活。转录因子 p65 可以通过结合 的启动子单独增加 的转录,并且在其结合位点发生突变或缺失后,这种促进作用消失。然后,我们检查了 PUFAs 对与 LPS 诱导的炎症相关的关键激酶的基因表达水平和蛋白丰度的影响。我们发现,LA 表现出促炎反应,而 ALA、EPA 和 DHA 通过调节 PRRs 的表达、IKK 和 p38 的磷酸化以及 p65 的核易位来诱导抗炎作用。总的来说,这项研究增进了我们对 PUFAs 调节非模型鱼类 LPS 诱导炎症的调控机制的理解。

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