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网格蛋白介导的内吞作用参与了秀丽隐杆线虫中二氧化硅纳米颗粒的摄取和毒性。

Clathrin-mediated endocytosis is involved in uptake and toxicity of silica nanoparticles in Caenohabditis elegans.

机构信息

School of Environmental Engineering, University of Seoul, 163 Siripdaero, Dongdaemun-gu, Seoul, 130-743, South Korea.

School of Environmental Engineering, University of Seoul, 163 Siripdaero, Dongdaemun-gu, Seoul, 130-743, South Korea.

出版信息

Chem Biol Interact. 2019 Sep 25;311:108774. doi: 10.1016/j.cbi.2019.108774. Epub 2019 Jul 29.

Abstract

Silica nanoparticles (SiNPs) are one of the popular nanomaterials used in industrial manufacturing, synthesis, engineering, and medicine. Recently, mechanisms underlying toxicity of silica nanoparticles have been reported; however, their uptake mechanisms have still not fully understood. In this study, toxicity of SiNPs was investigated in the nematode Caenohabditis elegans by using microarray and pathway analysis focusing the uptake mechanisms and their impact on toxicity. Physicochemical characterization of SiNPs was performed using dynamic light scattering (DLS) and zeta potential. No mortality was observed after 24 h exposure to SiNPs. However, reproductive ability was significantly reduced at the same concentrations. To ascertain a global mechanism of toxicity, microarray was conducted on C. elegans exposed to 10 mg/L SiNPs (20% reduction in reproductive ability). Microarray results indicated that genes involved in reproduction, such as msp (Major Sperm Protein) genes, were significantly downregulated in C. elegans exposed to SiNPs. Pathway analyses on differentially expressed genes (DEGs) revealed that endocytic pathway as a major pathway involved in the uptake of SiNPs. Involvement of endocytic pathway in the uptake of SiNPs was assessed using specific inhibitors (methyl-β-cyclodextrin, chlorpromazine, and LY294002 for caveolin-, clathrin-, and pinocytosis-mediated endocytosis, respectively). The inhibitor assay indicated that an internalization process facilitated by clathrin-mediated endocytosis is involved in the uptake of SiNPs. Functional analysis using endocytosis defective mutants, (i,e.  cav-1, cup-2, and chc-1) confirmed the role of endocytosis on the reproductive toxicity of SiNPs. Overall results suggest that clathrin-mediated endocytosis pathway is a potential mechanism of uptake of SiNPs in C. elegans that in turn, affects general toxic outcome, such as, decrease in reproductive ability.

摘要

硅纳米颗粒 (SiNPs) 是一种广泛应用于工业制造、合成、工程和医学的纳米材料。最近,已经报道了硅纳米颗粒毒性的作用机制,但它们的摄取机制仍未完全了解。在这项研究中,通过使用微阵列和途径分析,重点关注摄取机制及其对毒性的影响,研究了线虫秀丽隐杆线虫中 SiNPs 的毒性。使用动态光散射 (DLS) 和zeta 电位对 SiNPs 的理化特性进行了表征。在暴露于 SiNPs 24 小时后,没有观察到死亡率。然而,在相同浓度下,生殖能力显著降低。为了确定毒性的全局机制,对线虫暴露于 10mg/L SiNPs(生殖能力降低 20%)进行了微阵列分析。微阵列结果表明,暴露于 SiNPs 的线虫中,与生殖有关的基因,如 msp(主要精子蛋白)基因,显著下调。对差异表达基因 (DEGs) 的途径分析表明,内吞途径是 SiNPs 摄取的主要途径。使用特定抑制剂(甲基-β-环糊精、氯丙嗪和 LY294002 分别用于胞饮、网格蛋白和小窝蛋白介导的内吞作用)评估 SiNPs 摄取中内吞途径的参与。抑制剂测定表明,网格蛋白介导的内吞作用所促进的内化过程参与了 SiNPs 的摄取。使用内吞作用缺陷突变体(即 cav-1、cup-2 和 chc-1)进行功能分析,证实了内吞作用对 SiNPs 生殖毒性的作用。总体结果表明,网格蛋白介导的内吞途径是 SiNPs 在秀丽隐杆线虫中摄取的潜在机制,进而影响一般毒性结果,如生殖能力下降。

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