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Nanoparticle Labeling of Bone Marrow-Derived Rat Mesenchymal Stem Cells: Their Use in Differentiation and Tracking

机译:骨髓源性大鼠间充质干细胞的纳米标记:在分化和跟踪中的使用。

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摘要

Mesenchymal stem cells (MSCs) are promising candidates for cellular therapies due to their ability to migrate to damaged tissue without inducing immune reaction. Many techniques have been developed to trace MSCs and their differentiation efficacy; however, all of these methods have limitations. Conjugated polymer based water-dispersible nanoparticles (CPN) represent a new class of probes because they offer high brightness, improved photostability, high fluorescent quantum yield, and noncytotoxicity comparing to conventional dyes and quantum dots. We aimed to use this tool for tracing MSCs' fate in vitro and in vivo. MSC marker expression, survival, and differentiation capacity were assessed upon CPN treatment. Our results showed that after CPN labeling, MSC markers did not change and significant number of cells were found to be viable as revealed by MTT. Fluorescent signals were retained for 3 weeks after they were differentiated into osteocytes, adipocytes, and chondrocytes in vitro. We also showed that the labeled MSCs migrated to the site of injury and retained their labels in an in vivo liver regeneration model. The utilization of nanoparticle could be a promising tool for the tracking of MSCs in vivo and in vitro and therefore can be a useful tool to understand differentiation and homing mechanisms of MSCs.
机译:间充质干细胞(MSCs)由于能够迁移到受损组织而不会引起免疫反应,因此有望成为细胞疗法的候选者。已经开发了许多技术来追踪MSC及其分化功效。但是,所有这些方法都有局限性。基于共轭聚合物的水分散性纳米粒子(CPN)代表了一类新型探针,因为与常规染料和量子点相比,它们具有高亮度,改进的光稳定性,高荧光量子产率和无细胞毒性的特点。我们旨在使用该工具在体外和体内追踪MSC的命运。 CPN处理后评估了MSC标记的表达,存活率和分化能力。我们的结果表明,经CPN标记后,MSC标记没有改变,并且MTT揭示了许多细胞是可行的。荧光信号在体外分化为骨细胞,脂肪细胞和软骨细胞后,将保留3周。我们还表明,标记的MSC迁移到损伤部位,并在体内肝脏再生模型中保留了它们的标记。纳米粒子的利用可能是体内和体外追踪MSC的有前途的工具,因此可以成为了解MSC分化和归巢机制的有用工具。

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