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大黄鱼(Larimichthys crocea)免疫应答中Trim38的特性鉴定与功能分析:针对感染

Characterization and Functional Analysis of Trim38 in the Immune Response of the Large Yellow Croaker () Against Infection.

作者信息

Li Qiaoying, Wu Hongling, Huang Ying, Yekefenhazi Dinaer, Zou Wenzheng, Han Fang

机构信息

State Key Laboratory of Mariculture Breeding, Fisheries College, Jimei University, Xiamen 361000, China.

出版信息

Int J Mol Sci. 2025 Apr 27;26(9):4150. doi: 10.3390/ijms26094150.

Abstract

The large yellow croaker () is a cornerstone species in Chinese marine aquaculture, yet bacterial infections-particularly visceral white nodules disease (VWND) caused by -severely compromise its production. This study aimed to elucidate the immunoregulatory mechanisms of tripartite motif-containing protein 38 in the large yellow croaker () during bacterial infections, with an emphasis on host-pathogen interactions involving , to evaluate its potential for disease-resistant breeding applications. The full-length cDNA of was cloned and characterized, with structural analysis revealing a conserved domain architecture comprising RING, B-box, coiled-coil, and PRY-SPRY motifs. Functional characterization through overexpression in large yellow croaker kidney cells (PCK cells) demonstrated significant modulation of key immune-related pathways, including TGF-β, PI3K-Akt, IL-17, and PPAR. Notably, -mediated inhibition of NF-κB signaling was shown to downregulate pro-inflammatory cytokines (TNF-α, IL-6, IFN-γ), establishing its role as a negative regulator of inflammatory responses. These findings provide insights into the immune mechanisms of Trim38 in large yellow croakers and highlight its potential as a molecular target for disease resistance breeding. Future research should explore its broader functions, including its antiviral potential.

摘要

大黄鱼是中国海水养殖的基石性物种,但细菌感染,尤其是由[病原体名称未给出]引起的内脏白色结节病(VWND),严重影响其产量。本研究旨在阐明大黄鱼中含三联基序蛋白38在细菌感染期间的免疫调节机制,重点关注涉及[病原体名称未给出]的宿主-病原体相互作用,以评估其在抗病育种应用中的潜力。克隆并鉴定了[蛋白名称未给出]的全长cDNA,结构分析表明其具有由RING、B-box、卷曲螺旋和PRY-SPRY基序组成的保守结构域。通过在大黄鱼肾细胞(PCK细胞)中过表达[蛋白名称未给出]进行功能表征,结果表明关键免疫相关途径(包括TGF-β、PI3K-Akt、IL-17和PPAR)受到显著调节。值得注意的是,[蛋白名称未给出]介导的对NF-κB信号通路的抑制作用被证明可下调促炎细胞因子(TNF-α、IL-6、IFN-γ),确立了其作为炎症反应负调节因子的作用。这些发现为大黄鱼中Trim38的免疫机制提供了见解,并突出了其作为抗病育种分子靶点的潜力。未来的研究应探索其更广泛的功能,包括其抗病毒潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/275f/12071835/12fc06caee90/ijms-26-04150-g001.jpg

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