AFRL/711 HPW/RHPB, Wright-Patterson Air Force Base, Dayton, Ohio, USA.
Nat Protoc. 2010 Apr;5(4):744-57. doi: 10.1038/nprot.2010.2. Epub 2010 Mar 25.
We describe the use of transmission electron microscopy (TEM) for cellular ultrastructural examination of nanoparticle (NP)-exposed biomaterials. Preparation and imaging of electron-transparent thin cell sections with TEM provides excellent spatial resolution (approximately 1 nm), which is required to track these elusive materials. This protocol provides a step-by-step method for the mass-basis dosing of cultured cells with NPs, and the process of fixing, dehydrating, staining, resin embedding, ultramicrotome sectioning and subsequently visualizing NP uptake and translocation to specific intracellular locations with TEM. In order to avoid potential artifacts, some technical challenges are addressed. Based on our results, this procedure can be used to elucidate the intracellular fate of NPs, facilitating the development of biosensors and therapeutics, and provide a critical component for understanding NP toxicity. This protocol takes approximately 1 week.
我们描述了使用透射电子显微镜(TEM)对暴露于纳米颗粒(NP)的生物材料进行细胞超微结构检查。TEM 对电子透明的薄细胞切片的制备和成像提供了极好的空间分辨率(约 1nm),这是追踪这些难以捉摸的材料所必需的。该方案提供了一种基于质量的培养细胞与 NP 剂量的分步方法,以及固定、脱水、染色、树脂包埋、超薄切片和随后用 TEM 可视化 NP 摄取和向特定细胞内位置转移的过程。为了避免潜在的假象,解决了一些技术挑战。根据我们的结果,该程序可用于阐明 NPs 的细胞内命运,有助于开发生物传感器和治疗方法,并为理解 NP 毒性提供关键组成部分。该方案大约需要 1 周。