...
首页> 外文期刊>Toxicological sciences: An official journal of the Society of Toxicology >Subtilase cytotoxin activates MAP kinases through PERK and IRE1 branches of the unfolded protein response.
【24h】

Subtilase cytotoxin activates MAP kinases through PERK and IRE1 branches of the unfolded protein response.

机译:枯草杆菌蛋白酶通过未折叠的蛋白质应答的PERK和IRE1分支激活MAP激酶。

获取原文
获取原文并翻译 | 示例
           

摘要

Recent reports suggested involvement of mitogen-activated protein (MAP) kinases in the pathogenesis of Shiga toxin-induced hemolytic uremic syndrome (HUS). In the present study, we investigated a role for subtilase cytotoxin (SubAB), a possible trigger for HUS, in the regulation of MAP kinases. Treatment of cells with SubAB caused phosphorylation of c-Jun NH(2)-terminal kinase, extracellular signal-regulated kinase (ERK), and p38 MAP kinase. It was associated with activation of activator protein 1 (AP-1) and induction of AP-1-dependent transcription. SubAB induced the unfolded protein response (UPR) and consequently caused MAP kinase activation. SubAB led to induction of three major branches of the UPR, and the protein kinase-like endoplasmic reticulum kinase and inositol-requiring ER-to-nucleus signal kinase 1 pathways were responsible for the activation of MAP kinases. These results elucidated the potential of SubAB to trigger MAP kinase pathways via the UPR, which may contribute to the pathogenesis of Shiga toxin-induced HUS.
机译:最近的报道表明有丝分裂原活化蛋白(MAP)激酶参与志贺毒素诱导的溶血性尿毒症综合征(HUS)的发病机理。在本研究中,我们调查了枯草杆菌蛋白酶(SubAB)(可能是HUS的触发因素)在MAP激酶调节中的作用。用SubAB处理细胞会引起c-Jun NH(2)末端激酶,细胞外信号调节激酶(ERK)和p38 MAP激酶的磷酸化。它与激活蛋白1(AP-1)的激活和AP-1依赖性转录的诱导有关。 SubAB诱导了未折叠的蛋白质反应(UPR),因此引起MAP激酶激活。 SubAB导致了UPR的三个主要分支的诱导,而蛋白激酶样内质网激酶和需要肌醇的ER到核信号激酶1通路负责MAP激酶的激活。这些结果阐明了SubAB通过UPR触发MAP激酶途径的潜力,这可能有助于志贺毒素诱导的HUS的发病机理。

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