Dosumu Abiola N, Claire Sunil, Watson Luke S, Girio Patricia M, Osborne Shani A M, Pikramenou Zoe, Hodges Nikolas J
School of Biosciences, School of Chemistry, and Doctoral Training Centre in Physical Sciences for Health, The University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom.
JACS Au. 2021 Feb 22;1(2):174-186. doi: 10.1021/jacsau.0c00033. Epub 2021 Jan 19.
Optical microscopy techniques are ideal for live cell imaging for real-time nanoparticle tracking of nanoparticle localization. However, the quantification of nanoparticle uptake is usually evaluated by analytical methods that require cell isolation. Luminescent labeling of gold nanoparticles with transition metal probes yields particles with attractive photophysical properties, enabling cellular tracking using confocal and time-resolved microscopies. In the current study, gold nanoparticles coated with a red-luminescent ruthenium transition metal complex are used to quantify and track particle uptake and localization. Analysis of the red-luminescence signal from particles is used as a metric of cellular uptake, which correlates to total cellular gold and ruthenium content, independently measured and correlated by inductively coupled plasma mass spectrometry. Tracking of the luminescence signal provides evidence of direct diffusion of the nanoparticles across the cytoplasmic membrane with particles observed in the cytoplasm and mitochondria as nonclustered "free" nanoparticles. Electron microscopy and inhibition studies identified macropinocytosis of clusters of particles into endosomes as the major mechanism of uptake. Nanoparticles were tracked inside GFP-tagged cells by following the red-luminescence signal of the ruthenium complex. Tracking of the particles demonstrates their initial location in early endosomes and, later, in lysosomes and autophagosomes. Colocalization was quantified by calculating the Pearson's correlation coefficient between red and green luminescence signals and confirmed by electron microscopy. Accumulation of particles in autophagosomes correlated with biochemical evidence of active autophagy, but there was no evidence of detachment of the luminescent label or breakup of the gold core. Instead, accumulation of particles in autophagosomes caused organelle swelling, breakdown of the surrounding membranes, and endosomal release of the nanoparticles into the cytoplasm. The phenomenon of endosomal release has important consequences for the toxicity, cellular targeting, and therapeutic future applications of gold nanoparticles.
光学显微镜技术非常适合用于活细胞成像,以实时追踪纳米颗粒的定位。然而,纳米颗粒摄取的定量通常通过需要细胞分离的分析方法来评估。用过渡金属探针进行金纳米颗粒的发光标记可产生具有吸引人的光物理性质的颗粒,从而能够使用共聚焦显微镜和时间分辨显微镜进行细胞追踪。在本研究中,涂有红色发光钌过渡金属络合物的金纳米颗粒用于定量和追踪颗粒摄取及定位。对颗粒红色发光信号的分析用作细胞摄取的指标,这与通过电感耦合等离子体质谱独立测量并相关的细胞总金和钌含量相关。对发光信号的追踪提供了纳米颗粒直接穿过细胞质膜扩散的证据,在细胞质和线粒体中观察到颗粒为非聚集的“游离”纳米颗粒。电子显微镜和抑制研究确定颗粒簇的巨胞饮作用进入内体是主要的摄取机制。通过跟踪钌络合物的红色发光信号,在绿色荧光蛋白标记的细胞内追踪纳米颗粒。对颗粒的追踪表明它们最初位于早期内体中,随后位于溶酶体和自噬体中。通过计算红色和绿色发光信号之间的皮尔逊相关系数来定量共定位,并通过电子显微镜进行确认。颗粒在自噬体中的积累与活跃自噬的生化证据相关,但没有发光标记物脱离或金核破裂的证据。相反,颗粒在自噬体中的积累导致细胞器肿胀、周围膜的破裂以及纳米颗粒从内体释放到细胞质中。内体释放现象对金纳米颗粒的毒性、细胞靶向和治疗未来应用具有重要影响。