Department of Ophthalmology and Visual Sciences, Vanderbilt University School of Medicine, Nashville, TN, USA..
Pharma Research and Early Development, Roche Innovation Center Basel, F. Hoffmann-La Roche, Ltd., Basel, Switzerland.
Nanomedicine. 2018 Jan;14(1):63-71. doi: 10.1016/j.nano.2017.08.018. Epub 2017 Sep 7.
Vascular cell adhesion molecule 1 (VCAM-1) is an important inflammatory biomarker correlating with retinal disease progression. Thus, detection of VCAM-1 mRNA expression levels at an early disease stage could be an important predictive biomarker to assess the risk of disease progression and monitoring treatment response. We have developed VCAM-1 targeted antisense hairpin DNA-functionalized gold nanoparticles (AS-VCAM-1 hAuNP) for the real time detection of VCAM-1 mRNA expression levels in retinal endothelial cells. The AS-VCAM-1 hAuNP fluorescence enhancement clearly visualized the TNF-α induced cellular VCAM-1 mRNA levels with high signal to noise ratios compared to normal serum treated cells. The scrambled hAuNP probes were minimally detectable under same image acquisition conditions. Intracellular hAuNPs were detected using transmission electron microscopy (TEM) analysis of the intact cells. In addition, the AS-VCAM-1 hAuNP probes exhibited no acute toxicity to the retinal microvascular endothelial cells as measured by live-dead assay.
血管细胞黏附分子 1(VCAM-1)是一种与视网膜疾病进展相关的重要炎症生物标志物。因此,在疾病早期检测 VCAM-1 mRNA 的表达水平可能是评估疾病进展风险和监测治疗反应的重要预测生物标志物。我们已经开发了针对 VCAM-1 的反义发夹 DNA 功能化金纳米颗粒(AS-VCAM-1 hAuNP),用于实时检测视网膜内皮细胞中 VCAM-1 mRNA 的表达水平。与用正常血清处理的细胞相比,AS-VCAM-1 hAuNP 的荧光增强明显可视化了 TNF-α 诱导的细胞 VCAM-1 mRNA 水平,具有高信噪比。在相同的图像采集条件下,对乱序 hAuNP 探针的检测则非常低。通过对完整细胞的透射电子显微镜(TEM)分析检测到细胞内的 hAuNPs。此外,如通过死活检测所测量的,AS-VCAM-1 hAuNP 探针对视网膜微血管内皮细胞没有急性毒性。