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当新型氧化铁纳米颗粒 Molday ION Rhodamine B 标记人神经祖细胞时,其活力、表型、增殖和谱系分化得以保留。

Human neural progenitor cells retain viability, phenotype, proliferation, and lineage differentiation when labeled with a novel iron oxide nanoparticle, Molday ION Rhodamine B.

机构信息

Research Service, VA Maryland Health Care System, Baltimore, MD, USA ; Department of Pharmacology, University of Maryland School of Medicine, Baltimore, MD, USA.

Department of Pharmacology, University of Maryland School of Medicine, Baltimore, MD, USA ; Department of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, MD, USA.

出版信息

Int J Nanomedicine. 2013;8:4593-600. doi: 10.2147/IJN.S53012. Epub 2013 Nov 28.


DOI:10.2147/IJN.S53012
PMID:24348036
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3849141/
Abstract

Ultrasmall superparamagnetic iron-oxide particles (USPIOs) loaded into stem cells have been suggested as a way to track stem cell transplantation with magnetic resonance imaging, but the labeling, and post-labeling proliferation, viability, differentiation, and retention of USPIOs within the stem cells have yet to be determined for each type of stem cell and for each type of USPIO. Molday ION Rhodamine B™ (BioPAL, Worcester, MA, USA) (MIRB) has been shown to be a USPIO labeling agent for mesenchymal stem cells, glial progenitor cells, and stem cell lines. In this study, we have evaluated MIRB labeling in human neuroprogenitor cells and found that human neuroprogenitor cells are effectively labeled with MIRB without use of transfection reagents. Viability, proliferation, and differentiation properties are unchanged between MIRB-labeled neuroprogenitors cells and unlabeled cells. Moreover, MIRB-labeled human neuroprogenitor cells can be frozen, thawed, and replated without loss of MIRB or even without loss of their intrinsic biology. Overall, those results show that MIRB has advantageous properties that can be used for cell-based therapy.

摘要

超顺磁性氧化铁纳米颗粒(USPIO)负载到干细胞中已被提议用于通过磁共振成像来追踪干细胞移植,但每种类型的干细胞和每种类型的 USPIO 中 USPIO 的标记、标记后的增殖、活力、分化和保留情况仍有待确定。Molday ION Rhodamine B™(BioPAL,马萨诸塞州伍斯特市,美国)(MIRB)已被证明是间充质干细胞、神经前体细胞和干细胞系的 USPIO 标记试剂。在这项研究中,我们评估了 MIRB 在人神经祖细胞中的标记,发现人神经祖细胞可以有效地用 MIRB 标记,而无需使用转染试剂。MIRB 标记的神经祖细胞与未标记的细胞之间的活力、增殖和分化特性没有变化。此外,MIRB 标记的人神经祖细胞可以冷冻、解冻和再种植,而不会丢失 MIRB,甚至不会丢失其内在生物学特性。总的来说,这些结果表明 MIRB 具有可用于细胞治疗的优势特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d8/3849141/2669842b7fde/ijn-8-4593Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d8/3849141/400e8d692be2/ijn-8-4593Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d8/3849141/50e0fef07f7a/ijn-8-4593Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d8/3849141/2669842b7fde/ijn-8-4593Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d8/3849141/400e8d692be2/ijn-8-4593Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d8/3849141/50e0fef07f7a/ijn-8-4593Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d8/3849141/2669842b7fde/ijn-8-4593Fig3.jpg

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[2]
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[3]
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World J Stem Cells. 2021-9-26

[4]
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Int J Nanomedicine. 2021

[5]
Optimizing Stem Cell Therapy after Ischemic Brain Injury.

J Stroke. 2020-9

[6]
Magnetic resonance imaging of human neural stem cells in rodent and primate brain.

Stem Cells Transl Med. 2021-1

[7]
In vivo Cell Tracking Using Non-invasive Imaging of Iron Oxide-Based Particles with Particular Relevance for Stem Cell-Based Treatments of Neurological and Cardiac Disease.

Mol Imaging Biol. 2020-12

[8]
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[9]
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