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含金纳米颗粒的重链人铁蛋白的细胞摄取增强。

Enhanced Cellular Uptake of H-Chain Human Ferritin Containing Gold Nanoparticles.

作者信息

Moglia Italo, Santiago Margarita, Guerrero Simon, Soler Mónica, Olivera-Nappa Alvaro, Kogan Marcelo J

机构信息

Department of Pharmacological and Toxicological Chemistry, Faculty of Chemical and Pharmaceutical Sciences, University of Chile, Santiago 8380494, Chile.

ACCDiS-Advanced Center for Chronic Diseases, Faculty of Chemical and Pharmaceutical Sciences, University of Chile, Santiago 8380494, Chile.

出版信息

Pharmaceutics. 2021 Nov 19;13(11):1966. doi: 10.3390/pharmaceutics13111966.

Abstract

Gold nanoparticles (AuNP) capped with biocompatible layers have functional optical, chemical, and biological properties as theranostic agents in biomedicine. The ferritin protein containing in situ synthesized AuNPs has been successfully used as an effective and completely biocompatible nanocarrier for AuNPs in human cell lines and animal experiments in vivo. Ferritin can be uptaken by different cell types through receptor-mediated endocytosis. Despite these advantages, few efforts have been made to evaluate the toxicity and cellular internalization of AuNP-containing ferritin nanocages. In this work, we study the potential of human heavy-chain (H) and light-chain (L) ferritin homopolymers as nanoreactors to synthesize AuNPs and their cytotoxicity and cellular uptake in different cell lines. The results show very low toxicity of ferritin-encapsulated AuNPs on different human cell lines and demonstrate that efficient cellular ferritin uptake depends on the specific H or L protein chains forming the ferritin protein cage and the presence or absence of metallic cargo. Cargo-devoid apoferritin is poorly internalized in all cell lines, and the highest ferritin uptake was achieved with AuNP-loaded H-ferritin homopolymers in transferrin-receptor-rich cell lines, showing more than seven times more uptake than apoferritin.

摘要

包覆有生物相容性层的金纳米颗粒(AuNP)作为生物医学中的治疗诊断剂具有功能性光学、化学和生物学特性。含有原位合成金纳米颗粒的铁蛋白已成功用作人细胞系和体内动物实验中有效的、完全生物相容的金纳米颗粒纳米载体。铁蛋白可通过受体介导的内吞作用被不同细胞类型摄取。尽管有这些优点,但很少有人致力于评估含金纳米颗粒的铁蛋白纳米笼的毒性和细胞内化情况。在这项工作中,我们研究了人重链(H)和轻链(L)铁蛋白同聚物作为纳米反应器合成金纳米颗粒的潜力及其在不同细胞系中的细胞毒性和细胞摄取情况。结果表明,铁蛋白包裹的金纳米颗粒对不同人细胞系的毒性非常低,并证明细胞对铁蛋白的有效摄取取决于形成铁蛋白蛋白笼的特定H或L蛋白链以及金属货物的有无。无货物的脱铁铁蛋白在所有细胞系中的内化程度都很低,在富含转铁蛋白受体的细胞系中,装载金纳米颗粒的H-铁蛋白同聚物的铁蛋白摄取量最高,显示出比脱铁铁蛋白多七倍以上的摄取量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95cc/8623468/6f165f8c1239/pharmaceutics-13-01966-g001.jpg

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