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Tracking the endocytic pathway of recombinant protein toxin delivered by multiwalled carbon nanotubes

机译:跟踪多壁碳纳米管传递的重组蛋白毒素的内吞途径

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摘要

The endocytic pathway of a recombinant protein toxin, ricin A-chain (RTA), delivered by multiwalled carbon nanotubes (MWCNTs) was tracked in HeLa cells by tagging RTA with enhanced green fluorescent protein (EGFP). EGFP-RTA was found to accumulate in the endosome and to be retrogradely transported to the endoplasmic reticulum, from which it translocated into the cytosol. Nuclear staining, Z-axis scanning with a laser scanning confocal microscope (LSCM), and transmission electron microscopy (TEM) indicated that the RTA exerted its toxic effects. Endocytosis-inhibiting tests with LSCM and flow cytometry showed that MWCNT-EGFP-RTA conjugates penetrated cells principally via clathrin-mediated endocytosis. These studies are beneficial to understanding the MWCNT-based intracellular drug delivery mechanism and provide guidelines for designing promising MWCNT-based vectors for targeting diagnostic or therapeutic compounds, not only to specific cells, but even to specific cellular compartments.
机译:通过用增强的绿色荧光蛋白(EGFP)标记RTA,在HeLa细胞中跟踪了多壁碳纳米管(MWCNT)传递的重组蛋白毒素蓖麻毒蛋白A链(RTA)的内吞途径。发现EGFP-RTA积累在内体中,并逆行转运至内质网,并从中转移到胞质溶胶中。核染色,激光共聚焦显微镜(LSCM)的Z轴扫描和透射电子显微镜(TEM)表明RTA发挥了毒性作用。 LSCM和流式细胞仪的内吞抑制试验表明,MWCNT-EGFP-RTA结合物主要通过网格蛋白介导的内吞作用渗透细胞。这些研究有益于理解基于MWCNT的细胞内药物递送机制,并为设计有前途的基于MWCNT的载体提供指导,这些载体不仅针对特定细胞,甚至针对特定细胞区室,用于靶向诊断或治疗化合物。

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