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首页> 外文期刊>Journal of Biophotonics >Tracking mesenchymal stromal cells using an ultra-bright TAT-functionalized plasmonic-active nanoplatform
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Tracking mesenchymal stromal cells using an ultra-bright TAT-functionalized plasmonic-active nanoplatform

机译:使用超亮TAT功能化的等离激元活性纳米平台追踪间充质基质细胞

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摘要

High-resolution tracking of stem cells remains a challenging task. An ultra-bright contrast agent with extended intracellular retention is suitable for in vivo high-resolution tracking of stem cells following the implantation. Here, a plasmonic-active nanoplatform was developed for tracking mesenchymal stromal cells (MSCs) in mice. The nanoplatform consisted of TAT peptide-functionalized gold nanostars (TAT-GNS) that emit ultra-bright two-photon photoluminescence capable of tracking MSCs under high-resolution optical imaging. In vitro experiment showed TAT-GNS-labeled MSCs retained a similar differentiability to that of non-labeled MSCs controls. Due to their star shape, TAT-GNS exhibited greater intracellular retention than that of commercial Q-Tracker. In vivo imaging of TAT-GNS-labeled MSCs five days following intra-arterial injections in mice kidneys showed possible MSCs implantation in juxta-glomerular (JG) regions, but non-specifically in glomeruli and afferent arterioles as well. With future design to optimize GNS labeling specificity and clearance, plasmonic-active nanoplatforms may be a useful intracellular tracking tool for stem cell research.
机译:干细胞的高分辨率跟踪仍然是一项艰巨的任务。具有延长的细胞内滞留性的超亮造影剂适用于植入后干细胞的体内高分辨率追踪。在这里,等离子体活性纳米平台被开发用于跟踪小鼠间充质基质细胞(MSCs)。纳米平台由TAT肽功能化的金纳米星(TAT-GNS)组成,它们发射超亮的双光子光致发光,能够在高分辨率光学成像下跟踪MSC。体外实验表明,TAT-GNS标记的MSC保留了与未标记MSC对照相似的可分化性。由于其星形,TAT-GNS的细胞内滞留性比市售Q-Tracker高。在小鼠肾脏内动脉注射后五天,TAT-GNS标记的MSC的体内成像显示可能将MSC植入近肾小球(JG)区,但也非特异性地植入肾小球和传入小动脉。通过优化GNS标记特异性和清除率的未来设计,等离子活性纳米平台可能成为干细胞研究的有用的细胞内追踪工具。

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