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量子点不会改变胰腺干细胞的分化潜能,且在子细胞间随机分布。

Quantum Dots Do Not Alter the Differentiation Potential of Pancreatic Stem Cells and Are Distributed Randomly among Daughter Cells.

作者信息

Danner S, Benzin H, Vollbrandt T, Oder J, Richter A, Kruse C

机构信息

Fraunhofer Research Institution for Marine Biotechnology, 23562 Luebeck, Germany.

出版信息

Int J Cell Biol. 2013;2013:918242. doi: 10.1155/2013/918242. Epub 2013 Jul 24.

DOI:10.1155/2013/918242
PMID:23997768
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3742022/
Abstract

With the increasing relevance of cell-based therapies, there is a demand for cell-labeling techniques for in vitro and in vivo studies. For the reasonable tracking of transplanted stem cells in animal models, the usage of quantum dots (QDs) for sensitive cellular imaging has major advances. QDs could be delivered to the cytoplasm of the cells providing intense and stable fluorescence. Although QDs are emerging as favourable nanoparticles for bioimaging, substantial investigations are still required to consider their application for adult stem cells. Therefore, rat pancreatic stem cells (PSCs) were labeled with different concentrations of CdSe quantum dots (Qtracker 605 nanocrystals). The QD labeled PSCs showed normal proliferation and their usual spontaneous differentiation potential in vitro. The labeling of the cell population was concentration dependent, with increasing cell load from 5 nM QDs to 20 nM QDs. With time-lapse microscopy, we observed that the transmission of the QD particles during cell divisions was random, appearing as equal or unequal transmission to daughter cells. We report here that QDs offered an efficient and nontoxic way to label pancreatic stem cells without genetic modifications. In summary, QD nanocrystals are a promising tool for stem cell labeling and facilitate tracking of transplanted cells in animal models.

摘要

随着基于细胞的疗法的相关性日益增加,对用于体外和体内研究的细胞标记技术有了需求。为了在动物模型中合理追踪移植的干细胞,使用量子点(QD)进行灵敏的细胞成像有了重大进展。量子点可以递送至细胞的细胞质中,提供强烈且稳定的荧光。尽管量子点正成为用于生物成像的有利纳米颗粒,但仍需要大量研究来考虑它们在成体干细胞中的应用。因此,用不同浓度的CdSe量子点(Qtracker 605纳米晶体)标记大鼠胰腺干细胞(PSC)。量子点标记的胰腺干细胞在体外显示出正常的增殖及其通常的自发分化潜能。细胞群体的标记呈浓度依赖性,随着量子点浓度从5 nM增加到20 nM,细胞负载增加。通过延时显微镜观察,我们发现量子点颗粒在细胞分裂期间的传递是随机的,表现为向子细胞的均等或不均等传递。我们在此报告,量子点提供了一种无需基因改造即可有效且无毒地标记胰腺干细胞的方法。总之,量子点纳米晶体是一种用于干细胞标记的有前途的工具,并有助于在动物模型中追踪移植的细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/3742022/347b6456ca08/IJCB2013-918242.011.jpg
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J Nanosci Nanotechnol. 2012 Sep;12(9):6880-6. doi: 10.1166/jnn.2012.5855.
2
Multifactorial determinants that govern nanoparticle uptake by human endothelial cells under flow.多因素决定了人内皮细胞在流动状态下对纳米颗粒的摄取。
Int J Nanomedicine. 2012;7:2943-56. doi: 10.2147/IJN.S30624. Epub 2012 Jun 14.
3
Human salivary gland stem cells: isolation, propagation, and characterization.
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Nat Nanotechnol. 2016 May;11(5):479-86. doi: 10.1038/nnano.2015.338. Epub 2016 Feb 29.
4
In vivo tracking of human placenta derived mesenchymal stem cells in nude mice via ¹⁴C-TdR labeling.通过¹⁴C-胸腺嘧啶核苷标记在裸鼠体内追踪人胎盘来源的间充质干细胞
BMC Biotechnol. 2015 Jun 13;15:55. doi: 10.1186/s12896-015-0174-4.
5
Nanoparticle labeling identifies slow cycling human endometrial stromal cells.
Stem Cell Res Ther. 2014 Jul 4;5(4):84. doi: 10.1186/scrt473.
人唾液腺干细胞:分离、增殖及特性鉴定
Methods Mol Biol. 2012;879:403-42. doi: 10.1007/978-1-61779-815-3_25.
4
Quantum dots do not affect the behaviour of mouse embryonic stem cells and kidney stem cells and are suitable for short-term tracking.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。
PLoS One. 2012;7(3):e32650. doi: 10.1371/journal.pone.0032650. Epub 2012 Mar 5.
5
Cellular modulation of polymeric device surfaces: promise of adult stem cells for neuro-prosthetics.聚合物器件表面的细胞调节:成年干细胞在神经修复中的应用前景。
Front Neurosci. 2011 Oct 10;5:114. doi: 10.3389/fnins.2011.00114. eCollection 2011.
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9
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