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

机译:微生物鞘氨基酶诱导螺旋型刷界膜的RHOA介导的重组,并防止侵袭

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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:肠上皮细胞的顶端刷界膜(BBM)形成高度结构化和动态的环境界面,用于调节肠道微生物及其产品的细胞生理和阻断侵袭。 BBM如何动态地响应致病性和共生细菌信号可以定义肠道稳态和免疫功能。我们以前发现,在模型肠上皮中,通过外源细菌鞘氨基氨基酶(SMASE)将顶端膜鞘磷脂转化为神经酰胺酶(SMASE)免受霍乱毒素的内吞作用和毒性的影响。在这里,我们通过表明Smase诱导剧烈,可逆的,依赖于顶端皮质F-Actin网络的剧烈改变的动作机制。顶端膜神经酰胺的积累是必要的,并且足以诱导肌动蛋白表型,并且这种膜结构改变并被增强先天免疫功能,如抗侵袭的侵袭。

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