...
首页> 外文期刊>Scientific reports. >Recombinant Mtb9.8 of Mycobacterium bovis stimulates TNF-α and IL-1β secretion by RAW264.7 macrophages through activation of NF-κB pathway via TLR2
【24h】

Recombinant Mtb9.8 of Mycobacterium bovis stimulates TNF-α and IL-1β secretion by RAW264.7 macrophages through activation of NF-κB pathway via TLR2

机译:通过通过TLR2激活NF-κB途径,通过TLR2激活NF-κB途径刺激TNF-α和IL-1β分泌的重组MTB9.8刺激TNF-α和IL-1β分泌

获取原文
           

摘要

The Mtb9.8 antigenic protein of Mycobacterium bovis/Mycobacterium tuberculosis has been identified as a target of the T-cell response. However, the interaction of Mtb9.8 with Toll-like receptors (TLRs) and the relevant signaling pathways have not been fully clarified. In this study, recombinant Mtb9.8 (rMtb9.8) derived from M. bovis-stimulated RAW264.7 cells initiated the secretion of TNF-α and IL-1β in a dose-dependent manner. Blocking assays show that TLR2-neutralizing antibody decreases the production of TNF-α and IL-1β. Moreover, NF-κB activation is associated with TNF-α and IL-1β production by rMtb9.8 stimulation, and rMtb9.8 stimulation also induces the phosphorylation of NF-κB p65 at Ser536 and its rapid nuclear translocation in RAW264.7 cells. Furthermore, NF-κB luciferase activity is rapidly activated in response to rMtb9.8 in RAW264.7 cells and is also significantly increased in rMtb9.8-induced HEK293-TLR2. However, these activations were abrogated in cells with a dominant-negative mutation of NF-κB p65 and by treatment with anti-TLR2 antibody. We also find that rMtb9.8 induces the activation of IRF-1. These findings indicate that M. bovis-derived rMtb9.8 activates the NF-κB pathway via TLR2 in RAW264.7 cells. In particular, it phosphorylates NF-κB p65 at Ser536 and induces nuclear translocation, thereby leading to the production of TNF-α and IL-1β, which correlates with the induction of IRF-1.
机译:MTB9.8分枝杆菌/分枝杆菌结核病的抗原蛋白已被鉴定为T细胞反应的靶标。然而,尚未完全阐明MTB9.8与Toll样受体(TLR)和相关信号通路的相互作用。在该研究中,来自M.BOVIS刺激的Raw264.7细胞的重组MTB9.8(RMTB9.8)引发了以剂量依赖性方式引发TNF-α和IL-1β的分泌。阻断测定表明,TLR2中和抗体降低了TNF-α和IL-1β的产生。此外,NF-κB活化与RMTB9.8刺激的TNF-α和IL-1β产生相关,RMTB9.8刺激也诱导SER536的NF-κBP65的磷酸化及其RAW264.7细胞中的快速核易位。此外,响应于Raw264.7细胞中的RMTB9.8迅速激活NF-κB荧光素酶活性,并且在RMTB9.8诱导的HEK293-TLR2中也显着增加。然而,这些活性在具有NF-κBP65的显性阴性突变的细胞中消除,并通过用抗TLR2抗体治疗。我们还发现RMTB9.8引起了IRF-1的激活。这些发现表明,M. Bovis衍生的RMTB9.8通过RAW264.7细胞中通过TLR2激活NF-κB途径。特别地,它在Ser536磷酸化NF-κBP65并诱导核易位,从而导致TNF-α和IL-1β的产生,其与IRF-1的诱导相关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号