SRA5在黄斑部外侧的特征及初步免疫功能。

IF 3.9 2区 农林科学 Q1 FISHERIES Fish & shellfish immunology Pub Date : 2025-06-01 Epub Date: 2025-03-08 DOI:10.1016/j.fsi.2025.110266
Yangtao Peng , Changhong Lin , Bo Zhang , Lulu Yan , Bo Zhang , Chao Zhao , Lihua Qiu
{"title":"SRA5在黄斑部外侧的特征及初步免疫功能。","authors":"Yangtao Peng ,&nbsp;Changhong Lin ,&nbsp;Bo Zhang ,&nbsp;Lulu Yan ,&nbsp;Bo Zhang ,&nbsp;Chao Zhao ,&nbsp;Lihua Qiu","doi":"10.1016/j.fsi.2025.110266","DOIUrl":null,"url":null,"abstract":"<div><div>Scavenger receptors (SRs) are crucial for pattern recognition in the innate immune system. However, the role of <em>Scavenger Receptors class A member 5</em> (<em>SRA5</em>) in the immunological response of bony fish to pathogen invasion remains unclear. This study identified and characterized the <em>SRA5</em> of <em>Lateolabrax maculatus</em> (<em>LmSRA5</em>) from its transcriptome database. <em>LmSRA5</em> has a 1494 bp open reading frame, encodes 497 amino acids, has a molecular weight of 55.01 kDa, and contains a collagen domain and a conserved Scavenger Receptor Cysteine-Rich domain. <em>LmSRA5</em> exhibited high sequence similarity to previously reported <em>SRA5</em> genes. <em>LmSRA5</em> exhibited high sequence similarity to previously reported <em>SRA5</em> genes. <em>LmSRA5</em> is primarily localized in the cytoplasm, with its encoded proteins distributed in both the cytoplasm and the cell membrane. <em>LmSRA5</em> was expressed in all tissues. The highest expression was observed in the pituitary gland, with significant levels in the stomach, intestines, liver, and kidney. <em>LmSRA5</em> expression in the head kidney, spleen, blood, and intestines initially increased, then decreased following infection with <em>Aeromonas veronii</em>. The binding affinity of LmSRA5 for <em>A. veronii</em> was enhanced by increasing concentrations of the extracellular domain recombinant LmSRA5. Knockdown and overexpression experiments in liver cells demonstrated that <em>LmSRA5</em> significantly regulates the expression of <em>IL-8</em> and <em>c-Jun</em>. <em>LmSRA5</em> participates in the immune response by recognizing pathogen-associated molecular patterns (PAMPs) and contributes to immune regulation through modulation <em>IL-8</em> and <em>c-Jun</em>. This study offers valuable insights into the role of <em>SRA5</em> in pathogen resistance and immune regulation in bony fish, thereby contributing to the advancement of aquaculture under escalating disease pressures.</div></div>","PeriodicalId":12127,"journal":{"name":"Fish & shellfish immunology","volume":"161 ","pages":"Article 110266"},"PeriodicalIF":3.9000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Characteristics and preliminary immune function of SRA5 in Lateolabrax maculatus\",\"authors\":\"Yangtao Peng ,&nbsp;Changhong Lin ,&nbsp;Bo Zhang ,&nbsp;Lulu Yan ,&nbsp;Bo Zhang ,&nbsp;Chao Zhao ,&nbsp;Lihua Qiu\",\"doi\":\"10.1016/j.fsi.2025.110266\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Scavenger receptors (SRs) are crucial for pattern recognition in the innate immune system. However, the role of <em>Scavenger Receptors class A member 5</em> (<em>SRA5</em>) in the immunological response of bony fish to pathogen invasion remains unclear. This study identified and characterized the <em>SRA5</em> of <em>Lateolabrax maculatus</em> (<em>LmSRA5</em>) from its transcriptome database. <em>LmSRA5</em> has a 1494 bp open reading frame, encodes 497 amino acids, has a molecular weight of 55.01 kDa, and contains a collagen domain and a conserved Scavenger Receptor Cysteine-Rich domain. <em>LmSRA5</em> exhibited high sequence similarity to previously reported <em>SRA5</em> genes. <em>LmSRA5</em> exhibited high sequence similarity to previously reported <em>SRA5</em> genes. <em>LmSRA5</em> is primarily localized in the cytoplasm, with its encoded proteins distributed in both the cytoplasm and the cell membrane. <em>LmSRA5</em> was expressed in all tissues. The highest expression was observed in the pituitary gland, with significant levels in the stomach, intestines, liver, and kidney. <em>LmSRA5</em> expression in the head kidney, spleen, blood, and intestines initially increased, then decreased following infection with <em>Aeromonas veronii</em>. The binding affinity of LmSRA5 for <em>A. veronii</em> was enhanced by increasing concentrations of the extracellular domain recombinant LmSRA5. Knockdown and overexpression experiments in liver cells demonstrated that <em>LmSRA5</em> significantly regulates the expression of <em>IL-8</em> and <em>c-Jun</em>. <em>LmSRA5</em> participates in the immune response by recognizing pathogen-associated molecular patterns (PAMPs) and contributes to immune regulation through modulation <em>IL-8</em> and <em>c-Jun</em>. This study offers valuable insights into the role of <em>SRA5</em> in pathogen resistance and immune regulation in bony fish, thereby contributing to the advancement of aquaculture under escalating disease pressures.</div></div>\",\"PeriodicalId\":12127,\"journal\":{\"name\":\"Fish & shellfish immunology\",\"volume\":\"161 \",\"pages\":\"Article 110266\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fish & shellfish immunology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S105046482500155X\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/3/8 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"FISHERIES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fish & shellfish immunology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S105046482500155X","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/8 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"FISHERIES","Score":null,"Total":0}
引用次数: 0

摘要

在先天免疫系统中,清道夫受体(SRs)对模式识别至关重要。然而,清道夫受体A类成员5 (SRA5)在硬骨鱼对病原体入侵的免疫应答中的作用尚不清楚。本研究从斑痣Lateolabrax maculatus的转录组数据库中鉴定并鉴定了SRA5 (LmSRA5)。LmSRA5具有1494 bp的开放阅读框,编码497个氨基酸,分子量为55.01 kDa,包含一个胶原结构域和一个保守的Scavenger Receptor半胱氨酸丰富结构域。LmSRA5与先前报道的SRA5基因具有高度的序列相似性。LmSRA5与先前报道的SRA5基因具有高度的序列相似性。LmSRA5主要定位于细胞质,其编码蛋白分布在细胞质和细胞膜上。LmSRA5在所有组织中均有表达。垂体表达量最高,胃、肠、肝、肾表达量显著。感染维罗氏气单胞菌后,LmSRA5在头部肾脏、脾脏、血液和肠道中的表达先升高后降低。通过增加细胞外结构域重组LmSRA5的浓度,增强了LmSRA5对veronii的结合亲和力。肝细胞敲低和过表达实验表明,LmSRA5显著调节IL-8和c-Jun的表达。LmSRA5通过识别病原体相关分子模式(pathogen associated molecular patterns, PAMPs)参与免疫应答,并通过调节IL-8和c-Jun参与免疫调节。本研究为SRA5在硬骨鱼病原体抗性和免疫调节中的作用提供了有价值的见解,从而有助于在疾病压力不断上升的情况下推进水产养殖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Characteristics and preliminary immune function of SRA5 in Lateolabrax maculatus
Scavenger receptors (SRs) are crucial for pattern recognition in the innate immune system. However, the role of Scavenger Receptors class A member 5 (SRA5) in the immunological response of bony fish to pathogen invasion remains unclear. This study identified and characterized the SRA5 of Lateolabrax maculatus (LmSRA5) from its transcriptome database. LmSRA5 has a 1494 bp open reading frame, encodes 497 amino acids, has a molecular weight of 55.01 kDa, and contains a collagen domain and a conserved Scavenger Receptor Cysteine-Rich domain. LmSRA5 exhibited high sequence similarity to previously reported SRA5 genes. LmSRA5 exhibited high sequence similarity to previously reported SRA5 genes. LmSRA5 is primarily localized in the cytoplasm, with its encoded proteins distributed in both the cytoplasm and the cell membrane. LmSRA5 was expressed in all tissues. The highest expression was observed in the pituitary gland, with significant levels in the stomach, intestines, liver, and kidney. LmSRA5 expression in the head kidney, spleen, blood, and intestines initially increased, then decreased following infection with Aeromonas veronii. The binding affinity of LmSRA5 for A. veronii was enhanced by increasing concentrations of the extracellular domain recombinant LmSRA5. Knockdown and overexpression experiments in liver cells demonstrated that LmSRA5 significantly regulates the expression of IL-8 and c-Jun. LmSRA5 participates in the immune response by recognizing pathogen-associated molecular patterns (PAMPs) and contributes to immune regulation through modulation IL-8 and c-Jun. This study offers valuable insights into the role of SRA5 in pathogen resistance and immune regulation in bony fish, thereby contributing to the advancement of aquaculture under escalating disease pressures.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Fish & shellfish immunology
Fish & shellfish immunology 农林科学-海洋与淡水生物学
CiteScore
7.50
自引率
19.10%
发文量
750
审稿时长
68 days
期刊介绍: Fish and Shellfish Immunology rapidly publishes high-quality, peer-refereed contributions in the expanding fields of fish and shellfish immunology. It presents studies on the basic mechanisms of both the specific and non-specific defense systems, the cells, tissues, and humoral factors involved, their dependence on environmental and intrinsic factors, response to pathogens, response to vaccination, and applied studies on the development of specific vaccines for use in the aquaculture industry.
期刊最新文献
Edwardsiella tarda infection induces PANoptosis in gill cells of Japanese flounder Paralichthys olivaceus Effects of artificial diet on glycolytic pathway and immune response in mandarin fish (Siniperca chuatsi) In vitro and in vivo evaluation of Bacillus amyloliquefaciens E35 as prophylactic agents against Singapore grouper iridovirus In vitro evaluation of vitamin D3 as an antiviral and immune modulator against novel yellow catfish calcivirus (YcCV) in channel catfish kidney (CCK) cell line in aquaculture Structural and functional characterization of SIRT1 in Litopenaeus vannamei: A regulator of energy metabolism, antioxidant system, autophagy and resistance to bacterial infection
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1