Suppr超能文献

金纳米粒子和银纳米粒子影响人胚胎神经前体细胞的生长特性。

Gold- and silver nanoparticles affect the growth characteristics of human embryonic neural precursor cells.

机构信息

Institute of Clinical Sciences, Department of Ophthalmology, Lund University, Lund, Sweden.

出版信息

PLoS One. 2013;8(3):e58211. doi: 10.1371/journal.pone.0058211. Epub 2013 Mar 11.

Abstract

Rapid development of nanotechnologies and their applications in clinical research have raised concerns about the adverse effects of nanoparticles (NPs) on human health and environment. NPs can be directly taken up by organs exposed, but also translocated to secondary organs, such as the central nervous system (CNS) after systemic- or subcutaneous administration, or via the olfactory system. The CNS is particularly vulnerable during development and recent reports describe transport of NPs across the placenta and even into brain tissue using in vitro and in vivo experimental systems. Here, we investigated whether well-characterized commercial 20 and 80 nm Au- and AgNPs have an effect on human embryonic neural precursor cell (HNPC) growth. After two weeks of NP exposure, uptake of NPs, morphological features and the amount of viable and dead cells, proliferative cells (Ki67 immunostaining) and apoptotic cells (TUNEL assay), respectively, were studied. We demonstrate uptake of both 20 and 80 nm Au- and AgNPs respectively, by HNPCs during proliferation. A significant effect on the sphere size- and morphology was found for all cultures exposed to Au- and AgNPs. AgNPs of both sizes caused a significant increase in numbers of proliferating and apoptotic HNPCs. In contrast, only the highest dose of 20 nm AuNPs significantly affected proliferation, whereas no effect was seen on apoptotic cell death. Our data demonstrates that both Au- and AgNPs interfere with the growth profile of HNPCs, indicating the need of further detailed studies on the adverse effects of NPs on the developing CNS.

摘要

纳米技术的快速发展及其在临床研究中的应用引起了人们对纳米粒子(NPs)对人类健康和环境的不良影响的关注。NPs 可以被暴露的器官直接摄取,也可以在全身或皮下给药后转移到次级器官,如中枢神经系统(CNS),或者通过嗅觉系统。CNS 在发育过程中特别脆弱,最近的报告描述了 NPs 通过胎盘转运,甚至通过体外和体内实验系统进入脑组织。在这里,我们研究了经过充分表征的商业 20nm 和 80nmAu 和 AgNPs 是否对人胚胎神经前体细胞(HNPC)的生长有影响。在 NP 暴露两周后,研究了 NPs 的摄取、形态特征以及活细胞和死细胞的数量、增殖细胞(Ki67 免疫染色)和凋亡细胞(TUNEL 检测)。我们证明了 HNPC 在增殖过程中摄取了 20nm 和 80nm 的 Au 和 AgNPs。所有暴露于 Au 和 AgNPs 的培养物的球体大小和形态都受到显著影响。AgNPs 的两种大小都导致增殖和凋亡 HNPC 的数量显著增加。相比之下,只有最高剂量的 20nmAuNPs 显著影响增殖,而对凋亡细胞死亡没有影响。我们的数据表明,Au 和 AgNPs 都干扰了 HNPCs 的生长模式,表明需要进一步详细研究 NPs 对发育中的 CNS 的不良影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b311/3594300/699cf49d0796/pone.0058211.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验