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CD44 促进梭菌iota 家族毒素的中毒。

CD44 Promotes intoxication by the clostridial iota-family toxins.

机构信息

Integrated Toxicology Division, Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.

出版信息

PLoS One. 2012;7(12):e51356. doi: 10.1371/journal.pone.0051356. Epub 2012 Dec 7.

Abstract

Various pathogenic clostridia produce binary protein toxins associated with enteric diseases of humans and animals. Separate binding/translocation (B) components bind to a protein receptor on the cell surface, assemble with enzymatic (A) component(s), and mediate endocytosis of the toxin complex. Ultimately there is translocation of A component(s) from acidified endosomes into the cytosol, leading to destruction of the actin cytoskeleton. Our results revealed that CD44, a multifunctional surface protein of mammalian cells, facilitates intoxication by the iota family of clostridial binary toxins. Specific antibody against CD44 inhibited cytotoxicity of the prototypical Clostridium perfringens iota toxin. Versus CD44(+) melanoma cells, those lacking CD44 bound less toxin and were dose-dependently resistant to C. perfringens iota, as well as Clostridium difficile and Clostridium spiroforme iota-like, toxins. Purified CD44 specifically interacted in vitro with iota and iota-like, but not related Clostridium botulinum C2, toxins. Furthermore, CD44 knockout mice were resistant to iota toxin lethality. Collective data reveal an important role for CD44 during intoxication by a family of clostridial binary toxins.

摘要

各种致病性梭菌产生与人类和动物的肠道疾病有关的二元蛋白毒素。单独的结合/转运(B)成分与细胞表面的蛋白质受体结合,与酶(A)成分组装,并介导毒素复合物的内吞作用。最终,A 成分(s)从酸化的内体易位到细胞质中,导致肌动蛋白细胞骨架的破坏。我们的结果表明,哺乳动物细胞的多功能表面蛋白 CD44 有助于梭菌二元毒素的 iota 家族中毒。针对 CD44 的特异性抗体抑制了典型产气荚膜梭菌 iota 毒素的细胞毒性。与 CD44(+)黑素瘤细胞相比,缺乏 CD44 的细胞结合的毒素较少,并且对产气荚膜梭菌 iota 以及艰难梭菌和梭状芽孢杆菌 iota 样毒素呈剂量依赖性耐药。纯化的 CD44 特异性体外与 iota 和 iota 样毒素相互作用,但不与相关的肉毒梭菌 C2 毒素相互作用。此外,CD44 敲除小鼠对 iota 毒素的致死作用具有抗性。集体数据揭示了 CD44 在梭菌二元毒素家族中毒过程中的重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6beb/3517468/68b6e16ebaa9/pone.0051356.g001.jpg

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