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ML1 通过识别 LPS 并调节虾体内 AMP 的表达来抑制细菌感染。

ML1 suppresses bacterial infection by recognizing LPS and regulating AMP expression in shrimp.

机构信息

Key Laboratory of Inland Saline-alkaline Aquaculture, Ministry of Agriculture and Rural Affairs, Shanghai, China.

East China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Shanghai, China.

出版信息

Front Immunol. 2022 Dec 28;13:1088862. doi: 10.3389/fimmu.2022.1088862. eCollection 2022.

Abstract

Toll and Toll-like receptors (TLRs) play essential roles in the innate immunity of and mammals. Recent studies have revealed the presence of Toll-mediated immune signaling pathways in shrimp. However, the recognition and activation mechanism of Toll signaling pathways in crustaceans remain poorly understood due to the absence of key recognition molecules, such as peptidoglycan recognition proteins. Here, a novel MD2-related lipid-recognition (ML) member named ML1 was characterized in . We found that ML1 shared a similar 3D structure with human MD2 that could specifically recognize lipopolysaccharides (LPS) participating in LPS-mediated TLR4 signaling. was highly expressed in hemocytes and remarkably upregulated after challenge. Furthermore, the binding and agglutinating assays showed that ML1 possessed strong binding activities to LPS and its key portion lipid A as well as cells, and the binding of ML1 with bacterial cells led to the agglutination of bacteria, suggesting ML1 may act as a potential pathogen recognition protein upon interaction with LPS. Besides, coating with recombinant ML1 promoted bacterial clearance and increased the survival rate of bacterium-challenged shrimp. This result was further confirmed by RNAi experiments. The knockdown of remarkably suppressed the clearance of bacteria in hemolymph and decreased the survival rate of infected shrimp. Meanwhile, the silencing of severely impaired the expression of a few antimicrobial peptides (AMPs). These results demonstrated the significant correlation of bacterial clearance mediated by ML1 with the AMP expression. Interestingly, we found that ML1 interacted with the extracellular region of Toll2, which had been previously shown to participate in bacterial clearance by regulating AMP expression. Taken together, the proposed antibacterial model mediated by ML1 might be described as follows. ML1 acted as a potential recognition receptor for Gram-negative bacteria by binding to LPS, and then it activated Toll2-mediated signaling pathway by interacting with Toll2 to eliminate invading bacteria through producing specific AMPs. This study provided new insights into the recognition and activation mechanism of Toll signaling pathways of invertebrates and the defense functions of ML members.

摘要

Toll 和 Toll 样受体 (TLRs) 在 和哺乳动物的固有免疫中发挥重要作用。最近的研究表明,虾中存在 Toll 介导的免疫信号通路。然而,由于缺乏关键的识别分子,如肽聚糖识别蛋白,甲壳动物中 Toll 信号通路的识别和激活机制仍不清楚。在这里,我们在 中鉴定了一种新的 MD2 相关脂质识别 (ML) 成员 ML1。我们发现 ML1 与人类 MD2 具有相似的 3D 结构,可以特异性识别参与 TLR4 信号的脂多糖 (LPS)。 在血细胞中高度表达,并在 后显著上调。此外,结合和凝集试验表明,ML1 具有与 LPS 及其关键部分脂质 A 以及 细胞的强结合活性,并且 ML1 与细菌细胞的结合导致细菌的凝集,表明 ML1 可能在与 LPS 相互作用时作为一种潜在的病原体识别蛋白发挥作用。此外,用重组 ML1 包被 可促进细菌清除 并提高受细菌感染虾的存活率。通过 RNAi 实验进一步证实了这一结果。 的敲低显著抑制了血淋巴中细菌的清除,并降低了受感染虾的存活率。同时, 的沉默严重损害了几种抗菌肽 (AMPs) 的表达。这些结果表明,由 ML1 介导的细菌清除与 AMP 表达显著相关。有趣的是,我们发现 ML1 与 Toll2 的细胞外区域相互作用,先前的研究表明 Toll2 通过调节 AMP 表达参与细菌清除。综上所述,由 ML1 介导的抗菌模型可以描述如下。ML1 通过与 LPS 结合作为革兰氏阴性细菌的潜在识别受体,然后通过与 Toll2 相互作用激活 Toll2 介导的信号通路,通过产生特定的 AMPs 消除入侵细菌。这项研究为无脊椎动物 Toll 信号通路的识别和激活机制以及 ML 成员的防御功能提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4b/9832027/52e4bf7170d7/fimmu-13-1088862-g001.jpg

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