首页> 美国卫生研究院文献>Cell Regulation >The Association of Shiga-like Toxin with Detergent-resistant Membranes Is Modulated by Glucosylceramide and Is an Essential Requirement in the Endoplasmic Reticulum for a Cytotoxic Effect
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The Association of Shiga-like Toxin with Detergent-resistant Membranes Is Modulated by Glucosylceramide and Is an Essential Requirement in the Endoplasmic Reticulum for a Cytotoxic Effect

机译:志贺样毒素与耐洗涤剂膜的关联受葡萄糖基神经酰胺调节是内质网细胞毒性作用的基本要求。

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摘要

Receptor-mediated internalization to the endoplasmic reticulum (ER) and subsequent retro-translocation to the cytosol are essential sequential processes required for the productive intoxication of susceptible mammalian cells by Shiga-like toxin-1 (SLTx). Recently, it has been proposed that the observed association of certain ER-directed toxins and viruses with detergent-resistant membranes (DRM) may provide a general mechanism for their retrograde transport to endoplasmic reticulum (ER). Here, we show that DRM recruitment of SLTx bound to its globotriosylceramide (Gb3) receptor is mediated by the availability of other glycosphingolipids. Reduction in glucosylceramide (GlcCer) levels led to complete protection against SLTx and a reduced cell surface association of bound toxin with DRM. This reduction still allowed efficient binding and transport of the toxin to the ER. However, toxin sequestration within DRM of the ER was abolished under reduced GlcCer conditions, suggesting that an association of toxin with lipid microdomains or rafts in the ER (where these are defined by detergent insolubility) is essential for a later step leading to or involving retro-translocation of SLTx across the ER membrane. In support of this, we show that a number of ER residents, proteins intimately involved in the process of ER dislocation of misfolded proteins, are present in DRM.
机译:受体介导的内质网(ER)内在化和随后的逆向转运到胞质溶胶是志贺样毒素1(SLTx)对中毒哺乳动物细胞产生生产性毒性所必需的基本顺序过程。最近,已经提出,观察到的某些ER导向的毒素和病毒与去污剂抗性膜(DRM)的结合可能为它们逆行转运至内质网(ER)提供了一般机制。在这里,我们显示绑定到其globotriosylceramide(Gb3)受体的SLTx的DRM募集是由其他糖鞘脂的可用性介导的。葡萄糖基神经酰胺(GlcCer)水平的降低导致针对SLTx的完全保护以及结合毒素与DRM的细胞表面缔合减少。这种减少仍然允许毒素有效结合和转运至ER。但是,在降低的GlcCer条件下,消除了ER DRM中的毒素螯合,这表明毒素与ER中的脂质微区或筏(其中这些由去污剂不溶性定义)的关联对于导致或涉及逆转的后续步骤至关重要SLTx跨ER膜的移位。为了证明这一点,我们表明DRM中存在大量的ER居民,即与错误折叠的蛋白ER错位过程密切相关的蛋白质。

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