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黄芪多糖可预防大黄鱼巨噬细胞中已灭活的 Alg 致炎损伤。

Astragalus polysaccharides protect against inactivated Vibrio alginolyticus-induced inflammatory injury in macrophages of large yellow croaker.

机构信息

Key Laboratory of Marine Biotechnology of Fujian Province, Institute of Oceanology, Fujian Agriculture and Forestry University, Fuzhou, 350002, PR China.

Key Laboratory of Marine Biotechnology of Fujian Province, Institute of Oceanology, Fujian Agriculture and Forestry University, Fuzhou, 350002, PR China; University Key Lab for Integrated Chinese Traditional and Western Veterinary Medicine and Animal Healthcare in Fujian Province, Fujian Agriculture and Forestry University, Fuzhou, 350002, PR China.

出版信息

Fish Shellfish Immunol. 2022 Dec;131:95-104. doi: 10.1016/j.fsi.2022.09.077. Epub 2022 Oct 4.

Abstract

As an effective immunostimulant, Astragalus polysaccharides (APS) have been widely used in fish aquaculture, however, their action mechanisms remain poorly understood. In the present paper, the inflammatory macrophage model of large yellow croaker (Larimichthys crocea) was constructed by using formalin-inactivated Vibrio alginolyticus. Inactivated V. alginolyticus could cause cellular damage of primary head kidney macrophages (PKM) by decreasing cell activity and inducing reactive oxygen species (ROS) production and cell apoptosis. When PKM were pretreated with APS, the depressed cell activity induced by inactivated V. alginolyticus was significantly improved, and ROS overproduction and cell apoptosis were inhibited. Then the protection mechanism of APS was investigated by transcriptome analysis. After treated with inactivated V. alginolyticus, the expression of immune-related genes (TLR5s, TLR13, Clec4e, IKK, IκB, BCL-3, NF-κB2, REL, IL-1β, and IL-6) and pyroptosis-related genes (caspase-1, NLRP3, and NLRC3) in PKM were significantly up-regulated. However, APS pretreatment reversed the up-regulation of most of the above-mentioned genes, where TLR5s, BCL-3, REL, caspase-1, NLRP12, IL-1β, and IL-6 were significantly down-regulated compared with inactivated V. alginolyticus-treated group. These results suggested that APS could protect large yellow croaker PKM against inactivated V. alginolyticus-induced inflammatory injury, and may exert their protection effects by activating NF-κB and pyroptosis signaling pathways. These findings therefore advance our understanding of the immune regulation mechanism of APS in fish, and facilitate the application of APS in prevention and control of fish bacteriosis.

摘要

作为一种有效的免疫刺激剂,黄芪多糖(APS)已广泛应用于鱼类养殖,但它们的作用机制仍知之甚少。本研究采用福尔马林灭活的溶藻弧菌构建大黄鱼(Larimichthys crocea)炎症性巨噬细胞模型。灭活的溶藻弧菌可通过降低细胞活性、诱导活性氧(ROS)产生和细胞凋亡引起原代头肾巨噬细胞(PKM)的细胞损伤。当 PKM 用 APS 预处理时,可显著改善由灭活的溶藻弧菌引起的细胞活性下降,并抑制 ROS 过度产生和细胞凋亡。然后通过转录组分析研究 APS 的保护机制。用灭活的溶藻弧菌处理后,PKM 中免疫相关基因(TLR5s、TLR13、Clec4e、IKK、IκB、BCL-3、NF-κB2、REL、IL-1β和 IL-6)和细胞焦亡相关基因(caspase-1、NLRP3 和 NLRC3)的表达显著上调。然而,APS 预处理逆转了上述大多数基因的上调,与灭活的溶藻弧菌处理组相比,TLR5s、BCL-3、REL、caspase-1、NLRP12、IL-1β和 IL-6 的表达显著下调。这些结果表明 APS 可保护大黄鱼 PKM 免受灭活的溶藻弧菌诱导的炎症损伤,可能通过激活 NF-κB 和细胞焦亡信号通路发挥其保护作用。这些发现有助于深入了解 APS 在鱼类中的免疫调节机制,并促进 APS 在鱼类细菌性疾病的防治中的应用。

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