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牛巨噬细胞可感知大肠杆菌志贺毒素1。

Bovine macrophages sense Escherichia coli Shiga toxin 1.

作者信息

Menge Christian, Loos Daniela, Bridger Philip S, Barth Stefanie, Werling Dirk, Baljer Georg

机构信息

Institute of Hygiene and Infectious Diseases of Animals, Justus-Liebig University, Gießen, Germany

Institute of Hygiene and Infectious Diseases of Animals, Justus-Liebig University, Gießen, Germany.

出版信息

Innate Immun. 2015 Aug;21(6):655-64. doi: 10.1177/1753425915581215. Epub 2015 Apr 23.

Abstract

Shiga toxin (Stx)-producing Escherichia coli (STEC) infections in cattle are asymptomatic; however, Stx impairs the initiation of an adaptive immune response by targeting bovine peripheral and intraepithelial lymphocytes. As presumptive bovine mucosal macrophages (Mø) are also sensitive to Stx, STEC may even exert immune modulatory effects by acting on steps preceding lymphocyte activation at the Mø level. We therefore studied the expression of the Stx receptor (CD77), cellular phenotype and functions after incubation of primary bovine monocyte-derived Mø with purified Stx1. A significant portion of bovine Mø expressed CD77 on their surface, with the recombinant B-subunit of Stx1 binding to >50% of the cells. Stx1 down-regulated significantly surface expression of CD14, CD172a and co-stimulatory molecules CD80 and CD86 within 4 h of incubation, while MHC-II expression remained unaffected. Furthermore, incubation of Mø with Stx1 increased significantly numbers of transcripts for IL-4, IL-6, IL-10, IFN-γ, TNF-α, IL-8 and GRO-α but not for IL-12, TGF-β, MCP-1 and RANTES. In the course of bovine STEC infections, Stx1 appears to induce in Mø a mixed response pattern reminiscent of regulatory Mø, which may amplify the direct suppressive effect of the toxin on lymphocytes.

摘要

产志贺毒素(Stx)的大肠杆菌(STEC)感染牛后不表现出症状;然而,Stx通过靶向牛外周血淋巴细胞和上皮内淋巴细胞来损害适应性免疫反应的启动。由于推测牛黏膜巨噬细胞(Mø)也对Stx敏感,STEC甚至可能通过在Mø水平上作用于淋巴细胞激活之前的步骤来发挥免疫调节作用。因此,我们研究了原代牛单核细胞衍生的Mø与纯化的Stx1孵育后Stx受体(CD77)的表达、细胞表型和功能。相当一部分牛Mø在其表面表达CD77,Stx1的重组B亚基与超过50%的细胞结合。在孵育4小时内,Stx1显著下调了CD14、CD172a以及共刺激分子CD80和CD86的表面表达,而MHC-II的表达未受影响。此外,用Stx1孵育Mø显著增加了IL-4、IL-6、IL-10、IFN-γ、TNF-α、IL-8和GRO-α的转录本数量,但IL-12、TGF-β、MCP-1和RANTES的转录本数量未增加。在牛STEC感染过程中,Stx1似乎在Mø中诱导出一种类似于调节性Mø的混合反应模式,这可能会放大毒素对淋巴细胞的直接抑制作用。

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