首页> 美国卫生研究院文献>Cell Regulation >Microbial sphingomyelinase induces RhoA-mediated reorganization of the apical brush border membrane and is protective against invasion
【2h】

Microbial sphingomyelinase induces RhoA-mediated reorganization of the apical brush border membrane and is protective against invasion

机译:微生物鞘磷脂酶诱导RhoA介导的根尖刷缘膜重组并具有防入侵作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The apical brush border membrane (BBM) of intestinal epithelial cells forms a highly structured and dynamic environmental interface that serves to regulate cellular physiology and block invasion by intestinal microbes and their products. How the BBM dynamically responds to pathogenic and commensal bacterial signals can define intestinal homeostasis and immune function. We previously found that in model intestinal epithelium, the conversion of apical membrane sphingomyelin to ceramide by exogenous bacterial sphingomyelinase (SMase) protected against the endocytosis and toxicity of cholera toxin. Here we elucidate a mechanism of action by showing that SMase induces a dramatic, reversible, RhoA-dependent alteration of the apical cortical F-actin network. Accumulation of apical membrane ceramide is necessary and sufficient to induce the actin phenotype, and this coincides with altered membrane structure and augmented innate immune function as evidenced by resistance to invasion by Salmonella.
机译:肠上皮细胞的根尖刷状缘膜(BBM)形成了高度结构化和动态的环境界面,可用来调节细胞的生理功能并阻止肠内微生物及其产物的入侵。 BBM如何动态响应病原性和共生细菌信号可以定义肠道稳态和免疫功能。我们先前发现,在模型肠上皮中,外源细菌鞘磷脂酶(SMase)将顶膜鞘磷脂转化为神经酰胺可防止内毒素和霍乱毒素的毒性。在这里,我们通过显示SMase诱导了根尖皮质F-肌动蛋白网络的戏剧性,可逆的,RhoA依赖性改变来阐明其作用机理。顶膜神经酰胺的积累对于诱导肌动蛋白表型是必要和充分的,这与膜结构改变和先天免疫功能增强相吻合,如沙门氏菌对入侵的抵抗力所证明。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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