Suppr超能文献

一种新鉴定的扇贝 MyD88 与 TLR 相互作用并在先天免疫中发挥作用。

A newly identified scallop MyD88 interacts with TLR and functions in innate immunity.

机构信息

School of Agriculture, Ludong University, Yantai, 264025, China.

School of Agriculture, Ludong University, Yantai, 264025, China; Rushan Marine Economy and Development Center, Rushan, 264599, China.

出版信息

Fish Shellfish Immunol. 2024 Aug;151:109697. doi: 10.1016/j.fsi.2024.109697. Epub 2024 Jun 12.

Abstract

Myeloid differentiation factor-88 (MyD88) is a key adaptor of the toll-like receptor (TLR) signaling pathway and plays a crucial role in innate immune signal transduction in animals. However, the MyD88-mediated signal transduction mechanism in shellfish has not been well studied. In this study, a new MyD88 gene, CfMyD88-2, was identified in the Zhikong scallop, Chlamys farreri. The 1779 bp long open reading frame encodes 592 amino acids. The N-terminus of CfMyD88-2 contains a conserved death domain (DD), followed by a TIR (TLR/Interleukin-1 Receptor) domain. The results of the multi-sequence comparison showed that the TIR domain sequences were highly conserved. Phylogenetic analysis revealed that CfMyD88-2 was first associated with Mizuhopecten yessoensis MyD88-4 and Argopecten irradians MyD88-4. CfMyD88-2 mRNA was expressed in all scallop tissues, as detected by qRT-PCR, and the expression level was the highest in the mantle and hepatopancreas. In addition, CfMyD88-2 mRNA expression significantly increased after pathogen-associated molecular patterns (PAMPs, such as lipopolysaccharide, peptidoglycan, or polyinosinic-polycytidylic acid) stimulation. The results of the co-immunoprecipitation experiments in HEK293T cells showed that both CfMyD88-1 and CfMyD88-2 interacted with the TLR protein of scallops, suggesting the existence of more than one functional TLR-MyD88 signaling axis in scallops. Dual luciferase reporter gene assays indicated that the overexpressed CfMyD88-2 in HEK293T cells activated interferon (IFN) α, IFN-β, IFN-γ, and NF-κB reporter genes, indicating that the protein has multiple functions. The results of the subcellular localization experiment uncovered that CfMyD88-2 was mainly localized in the cytoplasm of human cells. In summary, the novel identified CfMyD88-2 can respond to the challenge of PAMPs, participate in TLR immune signaling, and may activate downstream effector genes such as NF-κB gene. These research results will be useful in advancing the theory of innate immunity in invertebrates and provide a reference for the selection of disease-resistant scallops in the future.

摘要

髓样分化因子 88(MyD88)是 Toll 样受体(TLR)信号通路的关键衔接子,在动物的固有免疫信号转导中发挥着重要作用。然而,贝类中的 MyD88 介导的信号转导机制尚未得到很好的研究。在本研究中,在栉孔扇贝(Chlamys farreri)中鉴定出一种新的 MyD88 基因,CfMyD88-2。该基因长 1779bp,开放阅读框编码 592 个氨基酸。CfMyD88-2 的 N 端含有一个保守的死亡结构域(DD),其后是一个 TIR(TLR/白细胞介素-1 受体)结构域。多序列比较的结果表明,TIR 结构域序列高度保守。系统进化分析表明,CfMyD88-2 首先与 Mizuhopecten yessoensis MyD88-4 和 Argopecten irradians MyD88-4 相关。qRT-PCR 检测显示 CfMyD88-2mRNA 在所有扇贝组织中均有表达,其在套膜和肝胰腺中的表达水平最高。此外,CfMyD88-2mRNA 表达在受到病原体相关分子模式(PAMPs,如脂多糖、肽聚糖或多聚肌苷酸-多聚胞苷酸)刺激后显著增加。在 HEK293T 细胞中的共免疫沉淀实验结果表明,CfMyD88-1 和 CfMyD88-2 均与扇贝的 TLR 蛋白相互作用,这表明扇贝中可能存在不止一条功能性 TLR-MyD88 信号轴。双荧光素酶报告基因检测表明,过表达的 CfMyD88-2 在 HEK293T 细胞中激活了干扰素(IFN)α、IFN-β、IFN-γ 和 NF-κB 报告基因,表明该蛋白具有多种功能。亚细胞定位实验的结果表明,CfMyD88-2 主要定位于人细胞的细胞质中。综上所述,新鉴定的 CfMyD88-2 可以对 PAMPs 的挑战做出反应,参与 TLR 免疫信号转导,并可能激活 NF-κB 基因等下游效应基因。这些研究结果将有助于推进无脊椎动物固有免疫理论的发展,并为未来筛选抗病扇贝提供参考。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验