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Receptor-mediated entry of diphtheria toxin into monkey kidney (Vero) cells: electron microscopic evaluation.

机译:受体介导的白喉毒素进入猴肾(Vero)细胞:电子显微镜评估。

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摘要

To express toxicity in living cells, diphtheria toxin (DT) must cross a membrane barrier and reach its target in the cytosol. Here we examine the entry of DT into the toxin-sensitive monkey kidney (Vero) cells. Using electron microscopy we directly demonstrated for the first time that DT is internalized by receptor-mediated endocytosis, i.e., via clathrin-coated pits, and enters the endosomal system. Methylamine, which is known to protect cells from DT, stopped the movement of toxin to coated areas of the cell membrane. In the presence of amine, prebound biotinyl-DT was internalized, but toxicity was inhibited. Biochemical evidence revealed that methylamine maintained toxin molecules at a site accessible to neutralization by antitoxin. The data suggest that DT entering Vero cells in the presence of methylamine is sequestered within the cell and does not express toxicity.
机译:为了在活细胞中表达毒性,白喉毒素(DT)必须穿过膜屏障并到达其在细胞溶胶中的靶标。在这里,我们检查了DT进入毒素敏感的猴肾(Vero)细胞的过程。我们使用电子显微镜首次直接证明了DT是通过受体介导的内吞作用(即通过网格蛋白包被的凹坑)内在化并进入内体系统的。已知可以保护细胞免受DT侵害的甲胺阻止了毒素向细胞膜涂层区域的移动。在胺的存在下,预先结合的生物素-DT被内在化,但是毒性被抑制。生化证据表明,甲胺将毒素分子保持在可被抗毒素中和的位置。数据表明在甲胺存在下进入维罗细胞的DT被隔离在细胞内,并且不表达毒性。

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