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Real-time imaging of VCAM-1 mRNA in TNF-α activated retinal microvascular endothelial cells using antisense hairpin-DNA functionalized gold nanoparticles

机译:使用反义发夹-DNA功能化的金纳米粒子对TNF-α激活的视网膜微血管内皮细胞中VCAM-1 mRNA的实时成像

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摘要

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.
机译:血管细胞粘附分子1(VCAM-1)是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功能化的金纳米颗粒(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。与正常血清处理的细胞相比,AS-VCAM-1 hAuNP荧光增强可以清晰地观察到TNF-α诱导的细胞VCAM-1 mRNA水平,且信噪比较高。在相同的图像采集条件下,加扰的hAuNP探针几乎无法检测到。使用完整细胞的透射电子显微镜(TEM)分析检测细胞内hAuNPs。另外,通过活死测定法,AS-VCAM-1 hAuNP探针对视网膜微血管内皮细胞无急性毒性。

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