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量子点不会影响小鼠胚胎干细胞和肾脏干细胞的行为,适合短期追踪。

Quantum dots do not affect the behaviour of mouse embryonic stem cells and kidney stem cells and are suitable for short-term tracking.

机构信息

Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.

出版信息

PLoS One. 2012;7(3):e32650. doi: 10.1371/journal.pone.0032650. Epub 2012 Mar 5.

Abstract

Quantum dots (QDs) are small nanocrystals widely used for labelling cells in order to enable cell tracking in complex environments in vitro, ex vivo and in vivo. They present many advantages over traditional fluorescent markers as they are resistant to photobleaching and have narrow emission spectra. Although QDs have been used effectively in cell tracking applications, their suitability has been questioned by reports showing they can affect stem cell behaviour and can be transferred to neighbouring cells. Using a variety of cellular and molecular biology techniques, we have investigated the effect of QDs on the proliferation and differentiation potential of two stem cell types: mouse embryonic stem cells and tissue-specific stem cells derived from mouse kidney. We have also tested if QDs released from living or dead cells can be taken up by neighbouring cells, and we have determined if QDs affect the degree of cell-cell fusion; this information is critical in order to assess the suitability of QDs for stem cell tracking. We show here that QDs have no effect on the viability, proliferation or differentiation potential of the two stem cell types. Furthermore, we show that the extent of transfer of QDs to neighbouring cells is <4%, and that QDs do not increase the degree of cell-cell fusion. However, although the QDs have a high labelling efficiency (>85%), they are rapidly depleted from both stem cell populations. Taken together, our results suggest that QDs are effective cell labelling probes that are suitable for short-term stem cell tracking.

摘要

量子点 (QDs) 是一种小纳米晶体,广泛用于标记细胞,以实现细胞在体外、体外用复杂环境中的跟踪。与传统荧光标记物相比,它们具有许多优势,因为它们具有抗光漂白性和窄的发射光谱。尽管 QDs 已有效地用于细胞跟踪应用,但有报道称它们会影响干细胞行为并可转移到邻近细胞,这对其适用性提出了质疑。我们使用各种细胞和分子生物学技术,研究了 QDs 对两种干细胞类型(小鼠胚胎干细胞和源自小鼠肾脏的组织特异性干细胞)的增殖和分化潜力的影响。我们还测试了来自活细胞或死细胞的 QDs 是否可以被邻近细胞摄取,以及 QDs 是否会影响细胞融合程度;这些信息对于评估 QDs 用于干细胞跟踪的适用性至关重要。我们在这里表明,QDs 对两种干细胞类型的活力、增殖或分化潜力没有影响。此外,我们表明 QDs 向邻近细胞的转移程度 <4%,并且 QDs 不会增加细胞融合程度。然而,尽管 QDs 具有高标记效率 (>85%),但它们会从两种干细胞群中迅速耗尽。总之,我们的结果表明,QDs 是有效的细胞标记探针,适用于短期干细胞跟踪。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a63/3293847/e9335ec78d2c/pone.0032650.g001.jpg

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