• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

猪嗜血杆菌性败血病时外周血单核细胞中 TLR2、Siglec-3 和 CD163 的表达增加。

TLR2, Siglec-3 and CD163 expressions on porcine peripheral blood monocytes are increased during sepsis caused by Haemophilus parasuis.

机构信息

Microbiology & Immunology Section, Animal Health Department, Faculty of Veterinary Medicine, University of León, Spain.

Porcine Immunology Laboratory, Biotechnology Department, INIA, Madrid, Spain.

出版信息

Comp Immunol Microbiol Infect Dis. 2019 Jun;64:31-39. doi: 10.1016/j.cimid.2019.02.001. Epub 2019 Feb 8.

DOI:10.1016/j.cimid.2019.02.001
PMID:31174697
Abstract

TLRs, Siglecs and CD163 are cell surface receptors that play an important role in immune response and sepsis. The objective of this study was to assess changes in the expression levels of several of these receptors (TLR2, TLR4, CD163, Siglec-1, Siglec-3, Siglec-5 and Siglec-10) on the surface of peripheral blood mononuclear cells from pigs with sepsis caused by Haemophilus parasuis. Flow cytometry was employed to analyze samples from an experimental infection and from cell cultures. A significant increase in CD163, TLR2 and Siglec-3 expression during infection was seen. However, in vitro exposure of peripheral blood monocytes to bacteria or sera from infected pigs did not increase the expression of these receptors. These changes may be due to recruitment of monocytes into the blood compartment in response to H. parasuis-induced sepsis.

摘要

TLRs、Siglecs 和 CD163 是细胞表面受体,它们在免疫反应和败血症中起着重要作用。本研究的目的是评估几种这些受体(TLR2、TLR4、CD163、Siglec-1、Siglec-3、Siglec-5 和 Siglec-10)在由副猪嗜血杆菌引起的败血症的猪外周血单核细胞表面的表达水平的变化。流式细胞术用于分析来自实验感染和细胞培养的样本。在感染过程中观察到 CD163、TLR2 和 Siglec-3 的表达显著增加。然而,体外将外周血单核细胞暴露于细菌或来自感染猪的血清并没有增加这些受体的表达。这些变化可能是由于副猪嗜血杆菌诱导的败血症导致单核细胞募集到血液中。

相似文献

1
TLR2, Siglec-3 and CD163 expressions on porcine peripheral blood monocytes are increased during sepsis caused by Haemophilus parasuis.猪嗜血杆菌性败血病时外周血单核细胞中 TLR2、Siglec-3 和 CD163 的表达增加。
Comp Immunol Microbiol Infect Dis. 2019 Jun;64:31-39. doi: 10.1016/j.cimid.2019.02.001. Epub 2019 Feb 8.
2
Changes in macrophage phenotype after infection of pigs with Haemophilus parasuis strains with different levels of virulence.不同毒力水平副猪嗜血杆菌感染猪后巨噬细胞表型的变化。
Infect Immun. 2013 Jul;81(7):2327-33. doi: 10.1128/IAI.00056-13. Epub 2013 Apr 15.
3
Molecular cloning of porcine Siglec-3, Siglec-5 and Siglec-10, and identification of Siglec-10 as an alternative receptor for porcine reproductive and respiratory syndrome virus (PRRSV).猪唾液酸结合免疫球蛋白样凝集素-3、唾液酸结合免疫球蛋白样凝集素-5和唾液酸结合免疫球蛋白样凝集素-10的分子克隆,以及唾液酸结合免疫球蛋白样凝集素-10作为猪繁殖与呼吸综合征病毒(PRRSV)替代受体的鉴定。
J Gen Virol. 2017 Aug;98(8):2030-2042. doi: 10.1099/jgv.0.000859. Epub 2017 Jul 26.
4
Immune response of porcine alveolar macrophages to a concurrent infection with porcine reproductive and respiratory syndrome virus and Haemophilus parasuis in vitro.猪肺泡巨噬细胞对猪繁殖与呼吸综合征病毒和副猪嗜血杆菌并发感染的体外免疫反应。
Vet Microbiol. 2015 Oct 22;180(1-2):28-35. doi: 10.1016/j.vetmic.2015.08.026. Epub 2015 Aug 29.
5
Blood cellular immune response in pigs immunized and challenged with Haemophilus parasuis.用副猪嗜血杆菌免疫和攻毒的猪的血细胞免疫反应
Res Vet Sci. 2009 Apr;86(2):230-4. doi: 10.1016/j.rvsc.2008.07.010. Epub 2008 Sep 9.
6
Haemophilus parasuis induces activation of NF-κB and MAP kinase signaling pathways mediated by toll-like receptors.副猪嗜血杆菌可诱导由Toll样受体介导的NF-κB和丝裂原活化蛋白激酶信号通路的激活。
Mol Immunol. 2015 Jun;65(2):360-6. doi: 10.1016/j.molimm.2015.02.016. Epub 2015 Feb 28.
7
Comparative assessment of the recognition of domain-specific CD163 monoclonal antibodies in human monocytes explains wide discrepancy in reported levels of cellular surface CD163 expression.比较评估对人类单核细胞中特定领域 CD163 单克隆抗体的识别,可解释报道的细胞表面 CD163 表达水平的巨大差异。
Immunobiology. 2011 Aug;216(8):882-90. doi: 10.1016/j.imbio.2011.02.001. Epub 2011 Feb 22.
8
CD163 and CD206 expression does not correlate with tolerance and cytokine production in LPS-tolerant human monocytes.CD163和CD206的表达与脂多糖耐受的人单核细胞中的耐受性和细胞因子产生无关。
Cytometry B Clin Cytom. 2017 May;92(3):192-199. doi: 10.1002/cyto.b.21321. Epub 2016 Feb 8.
9
Immunomodulatory activity of extracellular Hsp70 mediated via paired receptors Siglec-5 and Siglec-14.通过配对受体Siglec-5和Siglec-14介导的细胞外Hsp70的免疫调节活性。
EMBO J. 2015 Nov 12;34(22):2775-88. doi: 10.15252/embj.201591407. Epub 2015 Oct 12.
10
Siglec-5 and Siglec-14 are polymorphic paired receptors that modulate neutrophil and amnion signaling responses to group B Streptococcus.Siglec-5 和 Siglec-14 是多态配对受体,可调节中性粒细胞和羊膜对 B 族链球菌的信号反应。
J Exp Med. 2014 Jun 2;211(6):1231-42. doi: 10.1084/jem.20131853. Epub 2014 May 5.

引用本文的文献

1
A marker-free genetic manipulation method for Glaesserella parasuis strains developed by alternately culturing transformants at 37°C and 30°C.一种无标记基因操作方法,用于交替在 37°C 和 30°C 下培养转化体,从而开发副猪嗜血杆菌菌株。
BMC Biotechnol. 2024 Sep 3;24(1):60. doi: 10.1186/s12896-024-00887-w.
2
Quantitative analysis of the blood transcriptome of young healthy pigs and its relationship with subsequent disease resilience.年轻健康猪血液转录组的定量分析及其与后续疾病恢复力的关系。
BMC Genomics. 2021 Aug 12;22(1):614. doi: 10.1186/s12864-021-07912-8.
3
Sialidase of Augments Inflammatory Response via Desialylation and Abrogation of Negative Regulation of Siglec-5.
唾液酸酶通过去唾液酸化和取消 Siglec-5 的负调控来增强炎症反应。
Infect Immun. 2021 Apr 16;89(5). doi: 10.1128/IAI.00696-20.
4
Integration Analysis of mA-SNPs and eQTLs Associated With Sepsis Reveals Platelet Degranulation and Infection are Mediated by mA mRNA Methylation.与脓毒症相关的mA单核苷酸多态性和表达数量性状基因座的整合分析揭示血小板脱颗粒和感染由mA mRNA甲基化介导。
Front Genet. 2020 Feb 26;11:7. doi: 10.3389/fgene.2020.00007. eCollection 2020.
5
Polyamine Transport Protein PotD Protects Mice against and Elevates the Secretion of Pro-Inflammatory Cytokines of Macrophage via JNK-MAPK and NF-κB Signal Pathways through TLR4.多胺转运蛋白PotD通过TLR4经由JNK-MAPK和NF-κB信号通路保护小鼠免受侵害并提高巨噬细胞促炎细胞因子的分泌。
Vaccines (Basel). 2019 Dec 14;7(4):216. doi: 10.3390/vaccines7040216.